Team:UNIPV-Pavia/Protocols

From 2011.igem.org

(Difference between revisions)
Line 87: Line 87:
<h1> <span class="mw-headline" id="Media_.26_Antibiotics">Media &amp; Antibiotics</span></h1>
<h1> <span class="mw-headline" id="Media_.26_Antibiotics">Media &amp; Antibiotics</span></h1>
<h2> <span class="mw-headline" id="LB">LB</span></h2>
<h2> <span class="mw-headline" id="LB">LB</span></h2>
-
<li> Add:
+
<ul>
-
<li> 10 g/L NaCl
+
  <li> Add:
-
<li> 10 g/L Bacto-Tryptone
+
    <ul>
-
<li> 5 g/L Bacto-Yeast Extract
+
      <li> 10 g/L NaCl </li>
-
<li> ddH2O
+
      <li> 10 g/L Bacto-Tryptone </li>
-
   to a sterile pyrex bottle
+
      <li> 5 g/L Bacto-Yeast Extract </li>
-
  <ul>
+
      <li> ddH2O </li>
-
    <li> autoclave </li>
+
    </ul>
-
    <li> (add antibiotic when it reaches ~45°C) </li>
+
   </li>
-
    <li> store at +4°C </li>
+
</ul>
-
  </ul>
+
to a sterile pyrex bottle
-
  <div align="right"><small><a href="#indice">^top</a></small></div>
+
<ul>
-
  <p><br />
+
  <li> autoclave </li>
-
  </p>
+
  <li> (add antibiotic when it reaches ~45°C) </li>
-
  <h2> <span class="mw-headline" id="LB_Agar">LB Agar</span></h2>
+
  <li> store at +4°C </li>
-
  <p>&bull; Add: </p>
+
</ul>
-
   <ul>
+
<div align="right"><small><a href="#indice">^top</a></small></div>
-
     <li>
+
<p><br />
-
       <ul>
+
</p>
-
        <li> 10 g/L NaCl </li>
+
<h2> <span class="mw-headline" id="LB_Agar">LB Agar</span></h2>
-
        <li> 10 g/L Bacto-Tryptone </li>
+
<ul>
-
        <li> 5 g/L Bacto-Yeast Extract </li>
+
   <li> Add:
-
        <li> 15 g/L Bacto-Agar </li>
+
     <ul>
-
        <li> ddH2O </li>
+
       <li> 10 g/L NaCl </li>
-
      </ul>
+
      <li> 10 g/L Bacto-Tryptone </li>
-
    </li>
+
      <li> 5 g/L Bacto-Yeast Extract </li>
-
  </ul>
+
      <li> 15 g/L Bacto-Agar </li>
-
  <p>to a sterile 1L flask </p>
+
      <li> ddH2O </li>
-
  <ul>
+
    </ul>
-
    <li> autoclave </li>
+
  </li>
-
    <li> (add antibiotic when the agar becomes visible in the liquid, at about 45°C; shake gently to avoid bubbles) </li>
+
</ul>
-
    <li> pour into Petri plates and close them immediately </li>
+
<p>to a sterile 1L flask </p>
-
    <li> let them polymerize for ~2-3h </li>
+
<ul>
-
    <li> invert plates and wrap them with aluminium foil and store at +4°C </li>
+
  <li> autoclave </li>
-
  </ul>
+
  <li> (add antibiotic when the agar becomes visible in the liquid, at about 45°C; shake gently to avoid bubbles) </li>
-
  <div align="right"><small><a href="#indice">^top</a></small></div>
+
  <li> pour into Petri plates and close them immediately </li>
-
  <p><br />
+
  <li> let them polymerize for ~2-3h </li>
-
  </p>
+
  <li> invert plates and wrap them with aluminium foil and store at +4°C </li>
-
  <h2> <span class="mw-headline" id="SOB">SOB</span></h2>
+
</ul>
-
  <ul>
+
<div align="right"><small><a href="#indice">^top</a></small></div>
-
    <li> Add:
+
<p><br />
-
      <ul>
+
</p>
-
        <li> 5 g/L Bacto-Yeast Extract </li>
+
<h2> <span class="mw-headline" id="SOB">SOB</span></h2>
-
        <li> 20 g/L Bacto-Tryptone </li>
+
<ul>
-
        <li> 10mM NaCl </li>
+
  <li> Add:
-
        <li> 2.5mM KCl </li>
+
    <ul>
-
        <li> 10mM MgSO4 </li>
+
      <li> 5 g/L Bacto-Yeast Extract </li>
-
        <li> 10mM MgCl2 </li>
+
      <li> 20 g/L Bacto-Tryptone </li>
-
      </ul>
+
      <li> 10mM NaCl </li>
-
    </li>
+
      <li> 2.5mM KCl </li>
-
  </ul>
+
      <li> 10mM MgSO4 </li>
-
  <p>to a sterile pyrex bottle </p>
+
      <li> 10mM MgCl2 </li>
-
  <ul>
+
    </ul>
-
    <li> (optional: check that pH is ~6.8, otherwise adjust with NaOH) </li>
+
  </li>
-
    <li> autoclave </li>
+
</ul>
-
    <li> (add antibiotic when it reaches ~45°C) </li>
+
<p>to a sterile pyrex bottle </p>
-
    <li> store at +4°C </li>
+
<ul>
-
  </ul>
+
  <li> (optional: check that pH is ~6.8, otherwise adjust with NaOH) </li>
-
  <div align="right"><small><a href="#indice">^top</a></small></div>
+
  <li> autoclave </li>
-
  <p><br />
+
  <li> (add antibiotic when it reaches ~45°C) </li>
-
  </p>
+
  <li> store at +4°C </li>
-
  <h2> <span class="mw-headline" id="SOC">SOC</span></h2>
+
</ul>
-
  <ul>
+
<div align="right"><small><a href="#indice">^top</a></small></div>
-
    <li> Prepare SOB and add 20 ml of 1M glucose (prepare it dissolving 3.6 g of glucose in 20 ml of ddH2O). </li>
+
<p><br />
-
  </ul>
+
</p>
-
  <div align="right"><small><a href="#indice">^top</a></small></div>
+
<h2> <span class="mw-headline" id="SOC">SOC</span></h2>
-
  <p><br />
+
<ul>
-
  </p>
+
  <li> Prepare SOB and add 20 ml of 1M glucose (prepare it dissolving 3.6 g of glucose in 20 ml of ddH2O). </li>
-
  <h2> <span class="mw-headline" id="M9_supplemented_with_glycerol_.28M9gly.29">M9 supplemented with glycerol (M9gly)</span></h2>
+
</ul>
-
  <p>For 1L of medium, add: </p>
+
<div align="right"><small><a href="#indice">^top</a></small></div>
-
  <ul>
+
<p><br />
-
    <li> 734 ml of autoclaved (and cooled to Tamb, N.B. consider evaporation during autoclaving) ddH2O with a magnetic stirrer inside the bottle </li>
+
</p>
-
    <li> 5 ml of autoclaved 80% glycerol as carbon source </li>
+
<h2> <span class="mw-headline" id="M9_supplemented_with_glycerol_.28M9gly.29">M9 supplemented with glycerol (M9gly)</span></h2>
-
    <li> 100 ul of autoclaved or filtered (0.2um) CaCl2 1 M </li>
+
<p>For 1L of medium, add: </p>
-
    <li> 20 ml of 10% autoclaved casamino acids (dissolve 50 g in 500 ml = 10% stock) </li>
+
<ul>
-
    <li> 34 ml of filtered (0.2um) thiamine hydrochloride MW=337.27g/mol (340 mg in 34 ml) (keep in mind it is photosensitive) </li>
+
  <li> 734 ml of autoclaved (and cooled to Tamb, N.B. consider evaporation during autoclaving) ddH2O with a magnetic stirrer inside the bottle </li>
-
    <li> 2 ml of autoclaved MgSO4 1 M </li>
+
  <li> 5 ml of autoclaved 80% glycerol as carbon source </li>
-
    <li> 200 ml of autoclaved M9 salts 5x (dissolve 56.4 g in 1 liter ddH2O = 5x stock) </li>
+
  <li> 100 ul of autoclaved or filtered (0.2um) CaCl2 1 M </li>
-
    <li> shake the ddH2O with the magnetic stirrer and start adding the other solutions in sterility (each solution must be completely dissolved!) in the order listed above. </li>
+
  <li> 20 ml of 10% autoclaved casamino acids (dissolve 50 g in 500 ml = 10% stock) </li>
-
    <li> add antibiotic if needed </li>
+
  <li> 34 ml of filtered (0.2um) thiamine hydrochloride MW=337.27g/mol (340 mg in 34 ml) (keep in mind it is photosensitive) </li>
-
    <li> store at +4°C, protected from light </li>
+
  <li> 2 ml of autoclaved MgSO4 1 M </li>
-
  </ul>
+
  <li> 200 ml of autoclaved M9 salts 5x (dissolve 56.4 g in 1 liter ddH2O = 5x stock) </li>
-
  <p>NOTE: </p>
+
  <li> shake the ddH2O with the magnetic stirrer and start adding the other solutions in sterility (each solution must be completely dissolved!) in the order listed above. </li>
-
  <ul>
+
  <li> add antibiotic if needed </li>
-
    <li> M9 salts 5x, 10% casamino acids, MgSO4 1 M and CaCl2 1 M can be stored at +4°C. </li>
+
  <li> store at +4°C, protected from light </li>
-
    <li> glycerol 80% can be stored at room temperature. </li>
+
</ul>
-
    <li> thiamine hydrochloride (LIGHT SENSITIVE) is one-shot and must be prepared each time (keep in mind you loose some volume during filtration) </li>
+
<p>NOTE: </p>
-
  </ul>
+
<ul>
-
  <div align="right"><small><a href="#indice">^top</a></small></div>
+
  <li> M9 salts 5x, 10% casamino acids, MgSO4 1 M and CaCl2 1 M can be stored at +4°C. </li>
-
  <p><br />
+
  <li> glycerol 80% can be stored at room temperature. </li>
-
    <br />
+
  <li> thiamine hydrochloride (LIGHT SENSITIVE) is one-shot and must be prepared each time (keep in mind you loose some volume during filtration) </li>
-
  </p>
+
</ul>
-
  <h2> <span class="mw-headline" id="Antibiotics">Antibiotics</span></h2>
+
<div align="right"><small><a href="#indice">^top</a></small></div>
-
  <p>Stocks at -20°C freezer: </p>
+
<p><br />
-
  <ul>
+
  <br />
-
    <li> Ampicillin 100 mg/ml (in water) </li>
+
</p>
-
    <li> Kanamycin 50 mg/ml (in water) </li>
+
<h2> <span class="mw-headline" id="Antibiotics">Antibiotics</span></h2>
-
    <li> Chloramphenicol 34 mg/ml (in 100% ethanol) </li>
+
<p>Stocks at -20°C freezer: </p>
-
  </ul>
+
<ul>
-
  <p>These stocks are 1000x for high copy number plasmids.
+
  <li> Ampicillin 100 mg/ml (in water) </li>
-
    For low copy number plasmids, you should use these final concentrations in media: </p>
+
  <li> Kanamycin 50 mg/ml (in water) </li>
-
  <ul>
+
  <li> Chloramphenicol 34 mg/ml (in 100% ethanol) </li>
-
    <li> Ampicillin 50 ug/ml </li>
+
</ul>
-
    <li> Kanamycin 20 ug/ml </li>
+
<p>These stocks are 1000x for high copy number plasmids.
-
    <li> Chloramphenicol 12.5 ug/ml </li>
+
  For low copy number plasmids, you should use these final concentrations in media: </p>
-
  </ul>
+
<ul>
-
  <div align="right"><small><a href="#indice">^top</a></small></div>
+
  <li> Ampicillin 50 ug/ml </li>
-
  <p><br />
+
  <li> Kanamycin 20 ug/ml </li>
-
    <br />
+
  <li> Chloramphenicol 12.5 ug/ml </li>
-
  </p>
+
</ul>
-
  <h1> <span class="mw-headline" id="E._coli_transformation">E. coli transformation</span></h1>
+
<div align="right"><small><a href="#indice">^top</a></small></div>
-
  <h2> <span class="mw-headline" id="Transforming_home-made_competent_cells">Transforming home-made competent cells</span></h2>
+
<p><br />
-
  <ul>
+
  <br />
-
    <li> heat ligation at 65°C to inactivate T4 ligase </li>
+
</p>
-
    <li> thaw in ice a vial of TOP10 competent cells stored at -80°C </li>
+
<h1> <span class="mw-headline" id="E._coli_transformation">E. coli transformation</span></h1>
-
    <li> incubate a selective LB agar plate at 37°C </li>
+
<h2> <span class="mw-headline" id="Transforming_home-made_competent_cells">Transforming home-made competent cells</span></h2>
-
    <li> pipet 800ul of LB (without antibiotic) in a 15ml falcon tube and incubate it at 37°C </li>
+
<ul>
-
    <li> heat the water bath at 42°C </li>
+
  <li> heat ligation at 65°C to inactivate T4 ligase </li>
-
  </ul>
+
  <li> thaw in ice a vial of TOP10 competent cells stored at -80°C </li>
-
  <p><br />
+
  <li> incubate a selective LB agar plate at 37°C </li>
-
  </p>
+
  <li> pipet 800ul of LB (without antibiotic) in a 15ml falcon tube and incubate it at 37°C </li>
-
  <ul>
+
  <li> heat the water bath at 42°C </li>
-
    <li> add 1 ul (~3ng of DNA vector) of ligation to 100ul of thawed TOP10 </li>
+
</ul>
-
    <li> add parafilm and incubate in ice for 30 min </li>
+
<p><br />
-
    <li> heat shock at 42°C for 1 min </li>
+
</p>
-
    <li> incubate in ice for 2 min </li>
+
<ul>
-
    <li> transfer transformed bacteria to 800ul of pre-warmed LB </li>
+
  <li> add 1 ul (~3ng of DNA vector) of ligation to 100ul of thawed TOP10 </li>
-
    <li> incubate at 37°C, 220 rpm for 1 h </li>
+
  <li> add parafilm and incubate in ice for 30 min </li>
-
    <li> centrifuge at 2000 rpm, 25°C for 10 min </li>
+
  <li> heat shock at 42°C for 1 min </li>
-
    <li> take 750ul of supernatant and resuspend the pellet in the remaining LB (~150ul) </li>
+
  <li> incubate in ice for 2 min </li>
-
    <li> plate the entire culture and incubate the plate at 37°C overnight </li>
+
  <li> transfer transformed bacteria to 800ul of pre-warmed LB </li>
-
  </ul>
+
  <li> incubate at 37°C, 220 rpm for 1 h </li>
-
  <p>Variants: </p>
+
  <li> centrifuge at 2000 rpm, 25°C for 10 min </li>
-
  <ul>
+
  <li> take 750ul of supernatant and resuspend the pellet in the remaining LB (~150ul) </li>
-
    <li> if you transform a miniprep, add less than 3 ng in order to have single colonies </li>
+
  <li> plate the entire culture and incubate the plate at 37°C overnight </li>
-
    <li> if you use another home-made competent strain, the protocol is the same but you should consider the transformation efficiency to add a proper amount of DNA </li>
+
</ul>
-
    <li> if you use commercial Invitrogen TOP10 the protocol changes and it is reported below. </li>
+
<p>Variants: </p>
-
  </ul>
+
<ul>
-
  <div align="right"><small><a href="#indice">^top</a></small></div>
+
  <li> if you transform a miniprep, add less than 3 ng in order to have single colonies </li>
-
  <p><br />
+
  <li> if you use another home-made competent strain, the protocol is the same but you should consider the transformation efficiency to add a proper amount of DNA </li>
-
    <br />
+
  <li> if you use commercial Invitrogen TOP10 the protocol changes and it is reported below. </li>
-
  </p>
+
</ul>
-
  <h2> <span class="mw-headline" id="Transforming_commercial_competent_cells">Transforming commercial competent cells</span></h2>
+
<div align="right"><small><a href="#indice">^top</a></small></div>
-
  <p>(according to manufacturer's protocol) </p>
+
<p><br />
-
  <ul>
+
  <br />
-
    <li> heat ligation at 65°C to inactivate T4 ligase </li>
+
</p>
-
    <li> thaw in ice a vial of TOP10 competent cells stored at -80°C (one vial contains 50ul of cells) </li>
+
<h2> <span class="mw-headline" id="Transforming_commercial_competent_cells">Transforming commercial competent cells</span></h2>
-
    <li> incubate a selective LB agar plate at 37°C </li>
+
<p>(according to manufacturer's protocol) </p>
-
    <li> heat the water bath at 42°C </li>
+
<ul>
-
  </ul>
+
  <li> heat ligation at 65°C to inactivate T4 ligase </li>
-
  <ul>
+
  <li> thaw in ice a vial of TOP10 competent cells stored at -80°C (one vial contains 50ul of cells) </li>
-
    <li> dilute the ligation 1:50 (or 1:100) in ddH2O, in order to have less than 100pg/ul </li>
+
  <li> incubate a selective LB agar plate at 37°C </li>
-
    <li> add 1 ul of ligation (or less than 100pg of miniprepped DNA) to 25 or 50ul of thawed TOP10 </li>
+
  <li> heat the water bath at 42°C </li>
-
    <li> add parafilm and incubate in ice for 10 min </li>
+
</ul>
-
    <li> heat shock at 42°C for 1 min </li>
+
<ul>
-
    <li> incubate in ice for 2 min </li>
+
  <li> dilute the ligation 1:50 (or 1:100) in ddH2O, in order to have less than 100pg/ul </li>
-
    <li> add 250ul of SOC medium </li>
+
  <li> add 1 ul of ligation (or less than 100pg of miniprepped DNA) to 25 or 50ul of thawed TOP10 </li>
-
    <li> incubate at 37°C, 220 rpm for 1 h </li>
+
  <li> add parafilm and incubate in ice for 10 min </li>
-
    <li> plate 150ul of the culture and incubate the plate at 37°C overnight </li>
+
  <li> heat shock at 42°C for 1 min </li>
-
    <li> the remaining 150ul can be stored at +4°C </li>
+
  <li> incubate in ice for 2 min </li>
-
  </ul>
+
  <li> add 250ul of SOC medium </li>
-
  <div align="right"><small><a href="#indice">^top</a></small></div>
+
  <li> incubate at 37°C, 220 rpm for 1 h </li>
-
  <p><br />
+
  <li> plate 150ul of the culture and incubate the plate at 37°C overnight </li>
-
    <br />
+
  <li> the remaining 150ul can be stored at +4°C </li>
-
  </p>
+
</ul>
-
  <h1> <span class="mw-headline" id="E._coli_competent_cells_preparation">E. coli competent cells preparation</span></h1>
+
<div align="right"><small><a href="#indice">^top</a></small></div>
-
  <h2> <span class="mw-headline" id="H._Inoue_et_al._.281990.29.2C_High_efficiency_transformation_of_Escherichia_coli_with_plasmids.2C_Gene_96_23-28.">H. Inoue et al. (1990), High efficiency transformation of Escherichia coli with plasmids, Gene 96 23-28.</span></h2>
+
<p><br />
-
  <dl>
+
  <br />
-
    <dt> DAY1 </dt>
+
</p>
-
    <dd> inoculum 5-8 ul from -80°C stock in 5 ml of LB (37°C, 220 rpm ON); </dd>
+
<h1> <span class="mw-headline" id="E._coli_competent_cells_preparation">E. coli competent cells preparation</span></h1>
-
    <dt>DAY2 </dt>
+
<h2> <span class="mw-headline" id="H._Inoue_et_al._.281990.29.2C_High_efficiency_transformation_of_Escherichia_coli_with_plasmids.2C_Gene_96_23-28.">H. Inoue et al. (1990), High efficiency transformation of Escherichia coli with plasmids, Gene 96 23-28.</span></h2>
-
    <dd> dilution 1:1000 in SOB (flask, 18-25°C, 220 rpm ON); </dd>
+
<dl>
-
    <dt> DAY3 </dt>
+
  <dt> DAY1 </dt>
-
    <dd> pre-chill centrifuge at 4°C; </dd>
+
  <dd> inoculum 5-8 ul from -80°C stock in 5 ml of LB (37°C, 220 rpm ON); </dd>
-
    <dd> prepare TB (prepare 50 ml every 125 ml of SOB):
+
  <dt>DAY2 </dt>
-
      <dl>
+
  <dd> dilution 1:1000 in SOB (flask, 18-25°C, 220 rpm ON); </dd>
-
         <dd>
+
  <dt> DAY3 </dt>
 +
  <dd> pre-chill centrifuge at 4°C; </dd>
 +
  <dd> prepare TB (prepare 50 ml every 125 ml of SOB):
 +
    <dl>
 +
      <dd>
 +
         <ul>
 +
          <li> 15mM CaCl2 </li>
 +
          <li> 250mM KCl </li>
 +
          <li> 10mM (3 g/L) Pipes </li>
 +
          <li> adjust pH at 6.7 with KOH </li>
 +
          <li> 55mM (8.9 g/L) MnCl2 </li>
 +
          <li> filter (0.2 um) the solution and chill in 50 ml </li>
 +
        </ul>
 +
      </dd>
 +
    </dl>
 +
  </dd>
 +
  <dd> put the flask in ice when the culture reaches OD600=~0.05 (1mm pathlength – NanoDrop); </dd>
 +
  <dd> aliquot in pre-chilled 50 ml falcon tubes; </dd>
 +
  <dd> centrifuge at 2500g (4400rpm), 4°C, 10 min; </dd>
 +
  <dd> ICE: discard, resuspend in 40 ml of TB each 125 ml SOB, centrifuge as before; </dd>
 +
  <dd> ICE: discard, resuspend in 10 ml of TB each 125 ml SOB, add 700ul DMSO; </dd>
 +
  <dd> ICE: aliquot 100ul in pre-chilled 0.5ml tubes; </dd>
 +
  <dd> put in -80°C freezer; </dd>
 +
</dl>
 +
<p>ALWAYS TEST THE EFFICIENCY IN [CFU/ug] UNITS: transform 100ul of competent cells with 4ng of DNA and 100ul of competent cells without DNA (add 1ul of ddH2O), then plate on proper LB agar plates. </p>
 +
<p>This protocol has shown to work with: </p>
 +
<ul>
 +
  <li> DH5alpha (10^8 with 100ul of cells); </li>
 +
  <li> TOP10 (5*10^7 with 100ul of cells); </li>
 +
  <li> BW20767 (10^3 with 100ul of cells); </li>
 +
  <li> DB3.1 (5*10^4 with 100ul of cells); </li>
 +
</ul>
 +
<div align="right"><small><a href="#indice">^top</a></small></div>
 +
<p><br />
 +
  <br />
 +
</p>
 +
<h2> <span class="mw-headline" id="J._Sambrook.2C_E.F._Fritsch.2C_T._Maniatis_.281989.29">J. Sambrook, E.F. Fritsch, T. Maniatis (1989)</span></h2>
 +
<ul>
 +
  <li>DAY1
 +
    <ul>
 +
      <li>Inoculum 5-8 ul from -80°C stock in 5 ml of LB (37°C, 220 rpm ON). </li>
 +
    </ul>
 +
  </li>
 +
  <li>DAY2
 +
    <ul>
 +
      <li>Dilution 1:500 in LB (flask, 30-37°C, 220 rpm), monitor OD600 until it reaches 0.04 (1mm pathlength – NanoDrop, it should take from 3 to 5 hours); </li>
 +
      <li>prepare the proper amount of 50 ml tubes in ice and pre-chill the centrifuge; </li>
 +
      <li>when the culture reaches the right OD600, aliquot the culture in the pre-chilled tubes; </li>
 +
      <li>centrifuge (4000rpm, 4°C, 10min) and discard the supernatant; </li>
 +
      <li>for each 50 ml of culture, add 30 ml of MgCl2-CaCl2 solution (Buffer1) and resuspend the pellet; </li>
 +
      <li>centrifuge (4000rpm, 4°C, 10min) and discard the supernatant; </li>
 +
      <li>for each 50 ml of the original culture, add 2 ml of CaCl2 solution (Buffer2) and resuspend the pellet; </li>
 +
      <li>aliquot in 0.5 ml tubes and store at -80°C. </li>
 +
    </ul>
 +
  </li>
 +
</ul>
 +
<p>ALWAYS TEST THE EFFICIENCY IN [CFU/ug] UNITS </p>
 +
<dl>
 +
  <dt>Buffers preparation </dt>
 +
</dl>
 +
<ul>
 +
  <li>Buffer1: 80mM MgCl2, 20mM CaCl2 (e.g.: mix 8 ml MgCl2 1M, 2 ml CaCl2 1M and 90 ml ddH2O):
 +
    <ul>
 +
      <li>put ddH2O into a flask or a bottle and autoclave it; </li>
 +
      <li>add MgCl2 previously filter-sterilized (0,2 um) and CaCl2 previously autoclaved or filter-sterilized (0,2 um). </li>
 +
    </ul>
 +
  </li>
 +
  <li>Buffer2: 0.1 M CaCl2 and 15% of glycerol (e.g.: mix 100 mL of 1M CaCl2, 150 mL of 100% Glycerol and 750 mL of ddH2O):
 +
    <ul>
 +
      <li>put ddH2O and glycerol into a flask and autoclave it; </li>
 +
      <li>add CaCl2 previously autoclaved or filter-sterilized (0,2 um). </li>
 +
    </ul>
 +
  </li>
 +
</ul>
 +
<p>Keep Buffers cold. </p>
 +
<div align="right"><small><a href="#indice">^top</a></small></div>
 +
<p><br />
 +
  <br />
 +
</p>
 +
<h1> <span class="mw-headline" id="E._coli_strains_.28all_in_-80.C2.B0C_freezer.29">E. coli strains (all in -80°C freezer)</span></h1>
 +
<h2> <span class="mw-headline" id="TOP10">TOP10</span></h2>
 +
<p>F- mcrA Δ(mrr-hsdRMS-mcrBC) φ80lacZΔM15 ΔlacX74 nupG recA1 araD139 Δ(ara-leu)7697 galE15 galK16 rpsL(StrR) endA1 λ- </p>
 +
<ul>
 +
  <li> competent cells already prepared (5*10^7 CFU/ug with100ul of cells) </li>
 +
  <li> competent cells from Invitrogen available (10^9 CFU/ug with 50ul of cells) </li>
 +
  <li> commonly used for cloning and expression in our lab </li>
 +
  <li> they are equal to DH10B strain, whose genome is available from NCBI </li>
 +
</ul>
 +
<p>NOTE: they have </p>
 +
<ul>
 +
  <li> lacI wt </li>
 +
  <li> cI of phi80 prophage (different from cI of lambda phage) </li>
 +
  <li> Streptomycin resistance </li>
 +
</ul>
 +
<div align="right"><small><a href="#indice">^top</a></small></div>
 +
<h2> <span class="mw-headline" id="DH5alpha">DH5alpha</span></h2>
 +
<p>F- endA1 glnV44 thi-1 recA1 relA1 gyrA96 deoR nupG Φ80dlacZΔM15 Δ(lacZYA-argF)U169, hsdR17(rK- mK+), λ– </p>
 +
<ul>
 +
  <li> competent cells already prepared (10^8 CFU/ug with100ul of cells) </li>
 +
  <li> commonly used for cloning </li>
 +
</ul>
 +
<div align="right"><small><a href="#indice">^top</a></small></div>
 +
<h2> <span class="mw-headline" id="BW20767">BW20767</span></h2>
 +
<p>F-, RP4-2(Km::Tn7,Tc::Mu-1), leu-163::IS10, ΔuidA3::pir+, recA1, endA1, thi-1, hsdR17, creC510 </p>
 +
<ul>
 +
  <li> competent cells already prepared (10^3 CFU/ug with100ul of cells) </li>
 +
  <li> not used for cloning </li>
 +
</ul>
 +
<p>NOTE: they have </p>
 +
<ul>
 +
  <li> a fully working lac operon (already tested on IPTG/X-Gal plates) </li>
 +
  <li> Kan and Tet resistance (not tested) </li>
 +
</ul>
 +
<div align="right"><small><a href="#indice">^top</a></small></div>
 +
<h2> <span class="mw-headline" id="XL1-Blue">XL1-Blue</span></h2>
 +
<p>endA1 gyrA96(nalR) thi-1 recA1 relA1 lac glnV44 F'[&nbsp;::Tn10 proAB+ lacIq Δ(lacZ)M15] hsdR17(rK- mK+) </p>
 +
<ul>
 +
  <li> competent cells never prepared </li>
 +
  <li> a small stock of competent cells is available </li>
 +
  <li> used for cloning </li>
 +
</ul>
 +
<p>NOTE: they have lacIQ </p>
 +
<div align="right"><small><a href="#indice">^top</a></small></div>
 +
<h2> <span class="mw-headline" id="DB3.1">DB3.1</span></h2>
 +
<p>F- gyrA462 endA1 glnV44 Δ(sr1-recA) mcrB mrr hsdS20(rB-, mB-) ara14 galK2 lacY1 proA2 rpsL20(Smr) xyl5 Δleu mtl1 </p>
 +
<ul>
 +
  <li> competent cells already prepared (5*10^4 CFU/ug with 100ul of cells) </li>
 +
  <li> used for in vivo amplification of ccdB plasmids </li>
 +
</ul>
 +
<p>NOTE: they have a working lacZ, but a deleted lacY, they become slightly blue on IPTG/X-Gal plates </p>
 +
<div align="right"><small><a href="#indice">^top</a></small></div>
 +
<h2> <span class="mw-headline" id="STBL3">STBL3</span></h2>
 +
<p>F- glnV44 recA13 mcrB mrr hsdS20(rB-, mB-) ara-14 galK2 lacY1 proA2 rpsL20 xyl-5 leu mtl-1 </p>
 +
<ul>
 +
  <li> competent cells never prepared </li>
 +
  <li> used for in vivo amplification of DNA with direct repeats </li>
 +
</ul>
 +
<p>NOTE: they cannot be used for blue/white screening </p>
 +
<div align="right"><small><a href="#indice">^top</a></small></div>
 +
<h2> <span class="mw-headline" id="CW2553_.2B_pJat8">CW2553 + pJat8</span></h2>
 +
<p>Genotype: Khlebnikov A et al. (2000), Regulatable Arabinose-Inducible Gene Expression System with Consistent Control in All Cells of a Culture, Journal of Bacteriology, Vol. 182, No. 24, p.7029-7034. </p>
 +
<ul>
 +
  <li> pJat8 is Gentamycine resistant </li>
 +
</ul>
 +
<p>NOTE: </p>
 +
<ul>
 +
  <li> the stock of this strain has been grown without Gen </li>
 +
  <li> this strain is used for araBAD inducible system </li>
 +
</ul>
 +
<div align="right"><small><a href="#indice">^top</a></small></div>
 +
<h2> <span class="mw-headline" id="MG1655_.28seq.29">MG1655 (seq)</span></h2>
 +
<p>F-, λ-, rph-1 </p>
 +
<ul>
 +
  <li> CGSC#7740 </li>
 +
  <li> Fully sequenced genome (GenBank: NC_000913) </li>
 +
</ul>
 +
<div align="right"><small><a href="#indice">^top</a></small></div>
 +
<h2> <span class="mw-headline" id="MC1061">MC1061</span></h2>
 +
<p>F-, Δ(araA-leu)7697, [araD139]B/r, Δ(codB-lacI)3, galK16, galE15(GalS), λ-, e14-, mcrA0, relA1, rpsL150(strR), spoT1, mcrB1, hsdR2 </p>
 +
<ul>
 +
  <li> CGSC#6649 </li>
 +
</ul>
 +
<div align="right"><small><a href="#indice">^top</a></small></div>
 +
<h2> <span class="mw-headline" id="BW25141">BW25141</span></h2>
 +
<p>F-, Δ(araD-araB)567, ΔlacZ4787(::rrnB-3), Δ(phoB-phoR)580, λ-, galU95, ΔuidA3::pir+, recA1, endA9(del-ins)::FRT, rph-1, Δ(rhaD-rhaB)568, hsdR514 </p>
 +
<ul>
 +
  <li> CGSC#7635 </li>
 +
  <li> Carry the wild type pir gene </li>
 +
</ul>
 +
<div align="right"><small><a href="#indice">^top</a></small></div>
 +
<h2> <span class="mw-headline" id="BW25142">BW25142</span></h2>
 +
<p>F-, Δ(araD-araB)567, ΔlacZ4787(::rrnB-3), Δ(phoB-phoR)580, λ-, galU95, ΔuidA4::pir-116, recA1, endA9(del-ins)::FRT, rph-1, Δ(rhaD-rhaB)568, hsdR514 </p>
 +
<ul>
 +
  <li> CGSC#6649 </li>
 +
  <li> Carry the pir-116 gene </li>
 +
</ul>
 +
<div align="right"><small><a href="#indice">^top</a></small></div>
 +
<h2> <span class="mw-headline" id="BW23473">BW23473</span></h2>
 +
<p>F-, Δ(argF-lac)169, ΔuidA3::pir+, recA1, rpoS396(Am)?, endA9(del-ins)::FRT?, rph-1, hsdR514, rob-1, creC510 </p>
 +
<ul>
 +
  <li> CGSC#7837 </li>
 +
  <li> Carry the wild type pir gene </li>
 +
</ul>
 +
<div align="right"><small><a href="#indice">^top</a></small></div>
 +
<h2> <span class="mw-headline" id="BW23474">BW23474</span></h2>
 +
<p>F-, Δ(argF-lac)169, ΔuidA4::pir-116, recA1, rpoS396(Am)?, endA9(del-ins)::FRT, rph-1, hsdR514, rob-1, creC510 </p>
 +
<ul>
 +
  <li> CGSC#7838 </li>
 +
  <li> Carry the pir-116 gene </li>
 +
</ul>
 +
<div align="right"><small><a href="#indice">^top</a></small></div>
 +
<p><br />
 +
  <br />
 +
</p>
 +
<h1> <span class="mw-headline" id="Long_term_bacterial_glycerol_stocks">Long term bacterial glycerol stocks</span></h1>
 +
<ul>
 +
  <li> Mix 750 ul of a culture (preferably in log-phase) with 250 ul of 80% glycerol, in a 1.5ml vial </li>
 +
  <li> label the vial with name, date and antibiotic resistance </li>
 +
  <li> leave at -20°C for one day </li>
 +
  <li> move to -80°C the day after </li>
 +
</ul>
 +
<div align="right"><small><a href="#indice">^top</a></small></div>
 +
<p><br />
 +
  <br />
 +
</p>
 +
<h1> <span class="mw-headline" id="Plasmid_digestion_for_BioBrick_Standard_Assembly">Plasmid digestion for BioBrick Standard Assembly</span></h1>
 +
<dl>
 +
  <dt> To open vectors</dt>
 +
  <dd>
 +
    <ul>
 +
      <li> a volume containing 1 ug of purified plasmid </li>
 +
      <li> 2.5 ul of 10X buffer H </li>
 +
      <li> 1 ul of first enzyme </li>
 +
      <li> 1 ul of second enzyme </li>
 +
      <li> 25 ul final volume </li>
 +
      <li> incubate at 37°C for 3 hours </li>
 +
    </ul>
 +
  </dd>
 +
</dl>
 +
<dl>
 +
  <dt> To excide fragments</dt>
 +
  <dd>
 +
    <ul>
 +
      <li> A volume containing 1-1.8 ug of purified plasmid </li>
 +
      <li> 2.5 ul of buffer H </li>
 +
      <li> 1 ul of first enzyme </li>
 +
      <li> 1 ul of second enzyme </li>
 +
      <li> 25 ul final volume </li>
 +
      <li> incubate at 37°C for 3 hours </li>
 +
    </ul>
 +
  </dd>
 +
</dl>
 +
<p>NOTE: if you are performing a digestion for screening, 1 hour of incubation is sufficient. </p>
 +
<div align="right"><small><a href="#indice">^top</a></small></div>
 +
<p><br />
 +
  <br />
 +
</p>
 +
<h1> <span class="mw-headline" id="Ethanol_precipitation_with_sodium_acetate">Ethanol precipitation with sodium acetate</span></h1>
 +
<ul>
 +
  <li> Add 1/10 DNA solution volume of sodium acetate 3 M, pH 5.2 </li>
 +
  <li> Add 2.5 DNA solution volume of absolute ethanol </li>
 +
  <li> Freeze at -80°C for 30 min </li>
 +
  <li> Centrifuge at 13000 rpm, 4°C for 20 min </li>
 +
  <li> Decant supernatant </li>
 +
  <li> Add 250 µl of 70% ethanol </li>
 +
  <li> Centrifuge at 13000 rpm, 4°C for 20 min </li>
 +
  <li> Remove all supernatant with a pipette </li>
 +
  <li> Air dry pellet until ethanol is totally removed </li>
 +
  <li> Elute with 5-10 µl of ddH2O </li>
 +
</ul>
 +
<div align="right"><small><a href="#indice">^top</a></small></div>
 +
<p><br />
 +
  <br />
 +
</p>
 +
<h1> <span class="mw-headline" id="Ligation">Ligation</span></h1>
 +
<p>After the purification of two digested DNA fragments: </p>
 +
<ul>
 +
  <li> add a volume containing 20-50 ng of vector </li>
 +
  <li> add a volume containing: </li>
 +
</ul>
 +
<p><a href="/wiki/index.php?title=Special:Upload&amp;wpDestFile=Pv_formula_lig.png" class="new" title="File:Pv formula lig.png">File:Pv formula lig.png</a> </p>
 +
<p>("6" can be lowered to "2") </p>
 +
<ul>
 +
  <li> heat DNA mix at 65°C for 5 min for DNA denaturation </li>
 +
  <li> add 1 ul of T4 Ligase buffer (check if ATP is completely dissolved) </li>
 +
  <li> add 1 ul of T4 Ligase </li>
 +
  <li> 10-20 µl final volume </li>
 +
  <li> incubate at 16°C overnight </li>
 +
  <li> inactivate the T4 Ligase heating at 65°C for 10 min </li>
 +
  <li> then, ligation can be conserved at 4°C or can be transformed </li>
 +
</ul>
 +
<p>NOTE:
 +
  When the purified DNA of the insert also contains its native vector, you can perform the ligation anyway, but its antibiotic resistance must be different from the acceptor vector's resistance in order to select correct transformants on agar plates.
 +
  When doing this, you should modify the ligation protocol: </p>
 +
<ul>
 +
  <li> you should use "2" or "3" instead of "6" to compute the insert mass; </li>
 +
  <li> when you add the volume containing the insert mass, you must consider that the DNA quantification with NanoDrop refers to insert+NATIVE VECTOR. So, you must add: </li>
 +
</ul>
 +
<p><a href="/wiki/index.php?title=Special:Upload&amp;wpDestFile=Pv_formula_lig_2.jpeg" class="new" title="File:Pv formula lig 2.jpeg">File:Pv formula lig 2.jpeg</a> </p>
 +
<div align="right"><small><a href="#indice">^top</a></small></div>
 +
<p><br />
 +
  <br />
 +
</p>
 +
<h1> <span class="mw-headline" id="DNA_resuspension_from_iGEM_plates">DNA resuspension from iGEM plates</span></h1>
 +
<ul>
 +
  <li>Find the right position of the DNA of interest in iGEM plates </li>
 +
  <li>Resuspend with 15 ul ddH2O and transfer it in 0,5 ml sterile Eppendorf tubes </li>
 +
</ul>
 +
<p>Now you can store them at -20°C or transform in your favorite strain. </p>
 +
<div align="right"><small><a href="#indice">^top</a></small></div>
 +
<p><br />
 +
  <br />
 +
</p>
 +
<h1> <span class="mw-headline" id="PCR">PCR</span></h1>
 +
<ul>
 +
  <li>For every DNA sample you want to amplify, put:
 +
    <ul>
 +
      <li>2 µl buffer </li>
 +
      <li>0.6 µl MgCl2 </li>
 +
      <li>0.4 µl dNTPs </li>
 +
      <li>1 µl DNA (or ddH2O for blank sample). If you are performing a colony PCR, pick up the desired colony from a plate with a tip and dip it in the solution. </li>
 +
      <li>0.25 µl Taq Polymerase </li>
 +
      <li>0.5 ul VF2 primer (10 uM) </li>
 +
      <li>0.5 ul VR primer (10 uM) </li>
 +
      <li>A proper amount of ddH2O to have 20 µl of total reaction volume </li>
 +
    </ul>
 +
  </li>
 +
  <li>into an eppendorf tube. </li>
 +
  <li>Put the Eppendorf tube in the thermal cycler and set this program:
 +
    <ul>
 +
      <li>95°C 10 min </li>
 +
      <li>CYCLE:
 +
        <ul>
 +
          <li>95°C 30 sec </li>
 +
          <li>60°C 1 min </li>
 +
          <li>72°C 1-3 min </li>
 +
        </ul>
 +
      </li>
 +
      <li>for 35 cycles </li>
 +
      <li>72°C 7 min </li>
 +
      <li>16°C forever. </li>
 +
    </ul>
 +
  </li>
 +
  <li>Now you can add a loading buffer to the solution and perform electrophoresis to check the amplified sequence length. </li>
 +
</ul>
 +
<div align="right"><small><a href="#indice">^top</a></small></div>
 +
<p><br />
 +
  <br />
 +
</p>
 +
<h1> <span class="mw-headline" id="Electrophoresis">Electrophoresis</span></h1>
 +
<table>
 +
  <tr>
 +
    <td valign="top"><ul>
 +
        <li>Prepare agarose gel in 1x TBE buffer </li>
 +
        <li>Add ethidium bromide (using gloves and face mask for your safety):
           <ul>
           <ul>
-
             <li> 15mM CaCl2 </li>
+
             <li>1,5 µl in the small size agarose gel (70 ml) </li>
-
            <li> 250mM KCl </li>
+
            <li>3 µl in the middle size agarose gel (150 ml) </li>
-
            <li> 10mM (3 g/L) Pipes </li>
+
            <li>5 µl in the big size agarose gel (250 ml) </li>
-
            <li> adjust pH at 6.7 with KOH </li>
+
-
            <li> 55mM (8.9 g/L) MnCl2 </li>
+
-
            <li> filter (0.2 um) the solution and chill in 50 ml </li>
+
-
          </ul>
+
-
        </dd>
+
-
      </dl>
+
-
    </dd>
+
-
    <dd> put the flask in ice when the culture reaches OD600=~0.05 (1mm pathlength – NanoDrop); </dd>
+
-
    <dd> aliquot in pre-chilled 50 ml falcon tubes; </dd>
+
-
    <dd> centrifuge at 2500g (4400rpm), 4°C, 10 min; </dd>
+
-
    <dd> ICE: discard, resuspend in 40 ml of TB each 125 ml SOB, centrifuge as before; </dd>
+
-
    <dd> ICE: discard, resuspend in 10 ml of TB each 125 ml SOB, add 700ul DMSO; </dd>
+
-
    <dd> ICE: aliquot 100ul in pre-chilled 0.5ml tubes; </dd>
+
-
    <dd> put in -80°C freezer; </dd>
+
-
  </dl>
+
-
  <p>ALWAYS TEST THE EFFICIENCY IN [CFU/ug] UNITS: transform 100ul of competent cells with 4ng of DNA and 100ul of competent cells without DNA (add 1ul of ddH2O), then plate on proper LB agar plates. </p>
+
-
  <p>This protocol has shown to work with: </p>
+
-
  <ul>
+
-
    <li> DH5alpha (10^8 with 100ul of cells); </li>
+
-
    <li> TOP10 (5*10^7 with 100ul of cells); </li>
+
-
    <li> BW20767 (10^3 with 100ul of cells); </li>
+
-
    <li> DB3.1 (5*10^4 with 100ul of cells); </li>
+
-
  </ul>
+
-
  <div align="right"><small><a href="#indice">^top</a></small></div>
+
-
  <p><br />
+
-
    <br />
+
-
  </p>
+
-
  <h2> <span class="mw-headline" id="J._Sambrook.2C_E.F._Fritsch.2C_T._Maniatis_.281989.29">J. Sambrook, E.F. Fritsch, T. Maniatis (1989)</span></h2>
+
-
  <ul>
+
-
    <li>DAY1
+
-
      <ul>
+
-
        <li>Inoculum 5-8 ul from -80°C stock in 5 ml of LB (37°C, 220 rpm ON). </li>
+
-
      </ul>
+
-
    </li>
+
-
    <li>DAY2
+
-
      <ul>
+
-
        <li>Dilution 1:500 in LB (flask, 30-37°C, 220 rpm), monitor OD600 until it reaches 0.04 (1mm pathlength – NanoDrop, it should take from 3 to 5 hours); </li>
+
-
        <li>prepare the proper amount of 50 ml tubes in ice and pre-chill the centrifuge; </li>
+
-
        <li>when the culture reaches the right OD600, aliquot the culture in the pre-chilled tubes; </li>
+
-
        <li>centrifuge (4000rpm, 4°C, 10min) and discard the supernatant; </li>
+
-
        <li>for each 50 ml of culture, add 30 ml of MgCl2-CaCl2 solution (Buffer1) and resuspend the pellet; </li>
+
-
        <li>centrifuge (4000rpm, 4°C, 10min) and discard the supernatant; </li>
+
-
        <li>for each 50 ml of the original culture, add 2 ml of CaCl2 solution (Buffer2) and resuspend the pellet; </li>
+
-
        <li>aliquot in 0.5 ml tubes and store at -80°C. </li>
+
-
      </ul>
+
-
    </li>
+
-
  </ul>
+
-
  <p>ALWAYS TEST THE EFFICIENCY IN [CFU/ug] UNITS </p>
+
-
  <dl>
+
-
    <dt>Buffers preparation </dt>
+
-
  </dl>
+
-
  <ul>
+
-
    <li>Buffer1: 80mM MgCl2, 20mM CaCl2 (e.g.: mix 8 ml MgCl2 1M, 2 ml CaCl2 1M and 90 ml ddH2O):
+
-
      <ul>
+
-
        <li>put ddH2O into a flask or a bottle and autoclave it; </li>
+
-
        <li>add MgCl2 previously filter-sterilized (0,2 um) and CaCl2 previously autoclaved or filter-sterilized (0,2 um). </li>
+
-
      </ul>
+
-
    </li>
+
-
    <li>Buffer2: 0.1 M CaCl2 and 15% of glycerol (e.g.: mix 100 mL of 1M CaCl2, 150 mL of 100% Glycerol and 750 mL of ddH2O):
+
-
      <ul>
+
-
        <li>put ddH2O and glycerol into a flask and autoclave it; </li>
+
-
        <li>add CaCl2 previously autoclaved or filter-sterilized (0,2 um). </li>
+
-
      </ul>
+
-
    </li>
+
-
  </ul>
+
-
  <p>Keep Buffers cold. </p>
+
-
  <div align="right"><small><a href="#indice">^top</a></small></div>
+
-
  <p><br />
+
-
    <br />
+
-
  </p>
+
-
  <h1> <span class="mw-headline" id="E._coli_strains_.28all_in_-80.C2.B0C_freezer.29">E. coli strains (all in -80°C freezer)</span></h1>
+
-
  <h2> <span class="mw-headline" id="TOP10">TOP10</span></h2>
+
-
  <p>F- mcrA Δ(mrr-hsdRMS-mcrBC) φ80lacZΔM15 ΔlacX74 nupG recA1 araD139 Δ(ara-leu)7697 galE15 galK16 rpsL(StrR) endA1 λ- </p>
+
-
  <ul>
+
-
    <li> competent cells already prepared (5*10^7 CFU/ug with100ul of cells) </li>
+
-
    <li> competent cells from Invitrogen available (10^9 CFU/ug with 50ul of cells) </li>
+
-
    <li> commonly used for cloning and expression in our lab </li>
+
-
    <li> they are equal to DH10B strain, whose genome is available from NCBI </li>
+
-
  </ul>
+
-
  <p>NOTE: they have </p>
+
-
  <ul>
+
-
    <li> lacI wt </li>
+
-
    <li> cI of phi80 prophage (different from cI of lambda phage) </li>
+
-
    <li> Streptomycin resistance </li>
+
-
  </ul>
+
-
  <div align="right"><small><a href="#indice">^top</a></small></div>
+
-
  <h2> <span class="mw-headline" id="DH5alpha">DH5alpha</span></h2>
+
-
  <p>F- endA1 glnV44 thi-1 recA1 relA1 gyrA96 deoR nupG Φ80dlacZΔM15 Δ(lacZYA-argF)U169, hsdR17(rK- mK+), λ– </p>
+
-
  <ul>
+
-
    <li> competent cells already prepared (10^8 CFU/ug with100ul of cells) </li>
+
-
    <li> commonly used for cloning </li>
+
-
  </ul>
+
-
  <div align="right"><small><a href="#indice">^top</a></small></div>
+
-
  <h2> <span class="mw-headline" id="BW20767">BW20767</span></h2>
+
-
  <p>F-, RP4-2(Km::Tn7,Tc::Mu-1), leu-163::IS10, ΔuidA3::pir+, recA1, endA1, thi-1, hsdR17, creC510 </p>
+
-
  <ul>
+
-
    <li> competent cells already prepared (10^3 CFU/ug with100ul of cells) </li>
+
-
    <li> not used for cloning </li>
+
-
  </ul>
+
-
  <p>NOTE: they have </p>
+
-
  <ul>
+
-
    <li> a fully working lac operon (already tested on IPTG/X-Gal plates) </li>
+
-
    <li> Kan and Tet resistance (not tested) </li>
+
-
  </ul>
+
-
  <div align="right"><small><a href="#indice">^top</a></small></div>
+
-
  <h2> <span class="mw-headline" id="XL1-Blue">XL1-Blue</span></h2>
+
-
  <p>endA1 gyrA96(nalR) thi-1 recA1 relA1 lac glnV44 F'[&nbsp;::Tn10 proAB+ lacIq Δ(lacZ)M15] hsdR17(rK- mK+) </p>
+
-
  <ul>
+
-
    <li> competent cells never prepared </li>
+
-
    <li> a small stock of competent cells is available </li>
+
-
    <li> used for cloning </li>
+
-
  </ul>
+
-
  <p>NOTE: they have lacIQ </p>
+
-
  <div align="right"><small><a href="#indice">^top</a></small></div>
+
-
  <h2> <span class="mw-headline" id="DB3.1">DB3.1</span></h2>
+
-
  <p>F- gyrA462 endA1 glnV44 Δ(sr1-recA) mcrB mrr hsdS20(rB-, mB-) ara14 galK2 lacY1 proA2 rpsL20(Smr) xyl5 Δleu mtl1 </p>
+
-
  <ul>
+
-
    <li> competent cells already prepared (5*10^4 CFU/ug with 100ul of cells) </li>
+
-
    <li> used for in vivo amplification of ccdB plasmids </li>
+
-
  </ul>
+
-
  <p>NOTE: they have a working lacZ, but a deleted lacY, they become slightly blue on IPTG/X-Gal plates </p>
+
-
  <div align="right"><small><a href="#indice">^top</a></small></div>
+
-
  <h2> <span class="mw-headline" id="STBL3">STBL3</span></h2>
+
-
  <p>F- glnV44 recA13 mcrB mrr hsdS20(rB-, mB-) ara-14 galK2 lacY1 proA2 rpsL20 xyl-5 leu mtl-1 </p>
+
-
  <ul>
+
-
    <li> competent cells never prepared </li>
+
-
    <li> used for in vivo amplification of DNA with direct repeats </li>
+
-
  </ul>
+
-
  <p>NOTE: they cannot be used for blue/white screening </p>
+
-
  <div align="right"><small><a href="#indice">^top</a></small></div>
+
-
  <h2> <span class="mw-headline" id="CW2553_.2B_pJat8">CW2553 + pJat8</span></h2>
+
-
  <p>Genotype: Khlebnikov A et al. (2000), Regulatable Arabinose-Inducible Gene Expression System with Consistent Control in All Cells of a Culture, Journal of Bacteriology, Vol. 182, No. 24, p.7029-7034. </p>
+
-
  <ul>
+
-
    <li> pJat8 is Gentamycine resistant </li>
+
-
  </ul>
+
-
  <p>NOTE: </p>
+
-
  <ul>
+
-
    <li> the stock of this strain has been grown without Gen </li>
+
-
    <li> this strain is used for araBAD inducible system </li>
+
-
  </ul>
+
-
  <div align="right"><small><a href="#indice">^top</a></small></div>
+
-
  <h2> <span class="mw-headline" id="MG1655_.28seq.29">MG1655 (seq)</span></h2>
+
-
  <p>F-, λ-, rph-1 </p>
+
-
  <ul>
+
-
    <li> CGSC#7740 </li>
+
-
    <li> Fully sequenced genome (GenBank: NC_000913) </li>
+
-
  </ul>
+
-
  <div align="right"><small><a href="#indice">^top</a></small></div>
+
-
  <h2> <span class="mw-headline" id="MC1061">MC1061</span></h2>
+
-
  <p>F-, Δ(araA-leu)7697, [araD139]B/r, Δ(codB-lacI)3, galK16, galE15(GalS), λ-, e14-, mcrA0, relA1, rpsL150(strR), spoT1, mcrB1, hsdR2 </p>
+
-
  <ul>
+
-
    <li> CGSC#6649 </li>
+
-
  </ul>
+
-
  <div align="right"><small><a href="#indice">^top</a></small></div>
+
-
  <h2> <span class="mw-headline" id="BW25141">BW25141</span></h2>
+
-
  <p>F-, Δ(araD-araB)567, ΔlacZ4787(::rrnB-3), Δ(phoB-phoR)580, λ-, galU95, ΔuidA3::pir+, recA1, endA9(del-ins)::FRT, rph-1, Δ(rhaD-rhaB)568, hsdR514 </p>
+
-
  <ul>
+
-
    <li> CGSC#7635 </li>
+
-
    <li> Carry the wild type pir gene </li>
+
-
  </ul>
+
-
  <div align="right"><small><a href="#indice">^top</a></small></div>
+
-
  <h2> <span class="mw-headline" id="BW25142">BW25142</span></h2>
+
-
  <p>F-, Δ(araD-araB)567, ΔlacZ4787(::rrnB-3), Δ(phoB-phoR)580, λ-, galU95, ΔuidA4::pir-116, recA1, endA9(del-ins)::FRT, rph-1, Δ(rhaD-rhaB)568, hsdR514 </p>
+
-
  <ul>
+
-
    <li> CGSC#6649 </li>
+
-
    <li> Carry the pir-116 gene </li>
+
-
  </ul>
+
-
  <div align="right"><small><a href="#indice">^top</a></small></div>
+
-
  <h2> <span class="mw-headline" id="BW23473">BW23473</span></h2>
+
-
  <p>F-, Δ(argF-lac)169, ΔuidA3::pir+, recA1, rpoS396(Am)?, endA9(del-ins)::FRT?, rph-1, hsdR514, rob-1, creC510 </p>
+
-
  <ul>
+
-
    <li> CGSC#7837 </li>
+
-
    <li> Carry the wild type pir gene </li>
+
-
  </ul>
+
-
  <div align="right"><small><a href="#indice">^top</a></small></div>
+
-
  <h2> <span class="mw-headline" id="BW23474">BW23474</span></h2>
+
-
  <p>F-, Δ(argF-lac)169, ΔuidA4::pir-116, recA1, rpoS396(Am)?, endA9(del-ins)::FRT, rph-1, hsdR514, rob-1, creC510 </p>
+
-
  <ul>
+
-
    <li> CGSC#7838 </li>
+
-
    <li> Carry the pir-116 gene </li>
+
-
  </ul>
+
-
  <div align="right"><small><a href="#indice">^top</a></small></div>
+
-
  <p><br />
+
-
    <br />
+
-
  </p>
+
-
  <h1> <span class="mw-headline" id="Long_term_bacterial_glycerol_stocks">Long term bacterial glycerol stocks</span></h1>
+
-
  <ul>
+
-
    <li> Mix 750 ul of a culture (preferably in log-phase) with 250 ul of 80% glycerol, in a 1.5ml vial </li>
+
-
    <li> label the vial with name, date and antibiotic resistance </li>
+
-
    <li> leave at -20°C for one day </li>
+
-
    <li> move to -80°C the day after </li>
+
-
  </ul>
+
-
  <div align="right"><small><a href="#indice">^top</a></small></div>
+
-
  <p><br />
+
-
    <br />
+
-
  </p>
+
-
  <h1> <span class="mw-headline" id="Plasmid_digestion_for_BioBrick_Standard_Assembly">Plasmid digestion for BioBrick Standard Assembly</span></h1>
+
-
  <dl>
+
-
    <dt> To open vectors</dt>
+
-
    <dd>
+
-
      <ul>
+
-
        <li> a volume containing 1 ug of purified plasmid </li>
+
-
        <li> 2.5 ul of 10X buffer H </li>
+
-
        <li> 1 ul of first enzyme </li>
+
-
        <li> 1 ul of second enzyme </li>
+
-
        <li> 25 ul final volume </li>
+
-
        <li> incubate at 37°C for 3 hours </li>
+
-
      </ul>
+
-
    </dd>
+
-
  </dl>
+
-
  <dl>
+
-
    <dt> To excide fragments</dt>
+
-
    <dd>
+
-
      <ul>
+
-
        <li> A volume containing 1-1.8 ug of purified plasmid </li>
+
-
        <li> 2.5 ul of buffer H </li>
+
-
        <li> 1 ul of first enzyme </li>
+
-
        <li> 1 ul of second enzyme </li>
+
-
        <li> 25 ul final volume </li>
+
-
        <li> incubate at 37°C for 3 hours </li>
+
-
      </ul>
+
-
    </dd>
+
-
  </dl>
+
-
  <p>NOTE: if you are performing a digestion for screening, 1 hour of incubation is sufficient. </p>
+
-
  <div align="right"><small><a href="#indice">^top</a></small></div>
+
-
  <p><br />
+
-
    <br />
+
-
  </p>
+
-
  <h1> <span class="mw-headline" id="Ethanol_precipitation_with_sodium_acetate">Ethanol precipitation with sodium acetate</span></h1>
+
-
  <ul>
+
-
    <li> Add 1/10 DNA solution volume of sodium acetate 3 M, pH 5.2 </li>
+
-
    <li> Add 2.5 DNA solution volume of absolute ethanol </li>
+
-
    <li> Freeze at -80°C for 30 min </li>
+
-
    <li> Centrifuge at 13000 rpm, 4°C for 20 min </li>
+
-
    <li> Decant supernatant </li>
+
-
    <li> Add 250 µl of 70% ethanol </li>
+
-
    <li> Centrifuge at 13000 rpm, 4°C for 20 min </li>
+
-
    <li> Remove all supernatant with a pipette </li>
+
-
    <li> Air dry pellet until ethanol is totally removed </li>
+
-
    <li> Elute with 5-10 µl of ddH2O </li>
+
-
  </ul>
+
-
  <div align="right"><small><a href="#indice">^top</a></small></div>
+
-
  <p><br />
+
-
    <br />
+
-
  </p>
+
-
  <h1> <span class="mw-headline" id="Ligation">Ligation</span></h1>
+
-
  <p>After the purification of two digested DNA fragments: </p>
+
-
  <ul>
+
-
    <li> add a volume containing 20-50 ng of vector </li>
+
-
    <li> add a volume containing: </li>
+
-
  </ul>
+
-
  <p><a href="/wiki/index.php?title=Special:Upload&amp;wpDestFile=Pv_formula_lig.png" class="new" title="File:Pv formula lig.png">File:Pv formula lig.png</a> </p>
+
-
  <p>("6" can be lowered to "2") </p>
+
-
  <ul>
+
-
    <li> heat DNA mix at 65°C for 5 min for DNA denaturation </li>
+
-
    <li> add 1 ul of T4 Ligase buffer (check if ATP is completely dissolved) </li>
+
-
    <li> add 1 ul of T4 Ligase </li>
+
-
    <li> 10-20 µl final volume </li>
+
-
    <li> incubate at 16°C overnight </li>
+
-
    <li> inactivate the T4 Ligase heating at 65°C for 10 min </li>
+
-
    <li> then, ligation can be conserved at 4°C or can be transformed </li>
+
-
  </ul>
+
-
  <p>NOTE:
+
-
    When the purified DNA of the insert also contains its native vector, you can perform the ligation anyway, but its antibiotic resistance must be different from the acceptor vector's resistance in order to select correct transformants on agar plates.
+
-
    When doing this, you should modify the ligation protocol: </p>
+
-
  <ul>
+
-
    <li> you should use "2" or "3" instead of "6" to compute the insert mass; </li>
+
-
    <li> when you add the volume containing the insert mass, you must consider that the DNA quantification with NanoDrop refers to insert+NATIVE VECTOR. So, you must add: </li>
+
-
  </ul>
+
-
  <p><a href="/wiki/index.php?title=Special:Upload&amp;wpDestFile=Pv_formula_lig_2.jpeg" class="new" title="File:Pv formula lig 2.jpeg">File:Pv formula lig 2.jpeg</a> </p>
+
-
  <div align="right"><small><a href="#indice">^top</a></small></div>
+
-
  <p><br />
+
-
    <br />
+
-
  </p>
+
-
  <h1> <span class="mw-headline" id="DNA_resuspension_from_iGEM_plates">DNA resuspension from iGEM plates</span></h1>
+
-
  <ul>
+
-
    <li>Find the right position of the DNA of interest in iGEM plates </li>
+
-
    <li>Resuspend with 15 ul ddH2O and transfer it in 0,5 ml sterile Eppendorf tubes </li>
+
-
  </ul>
+
-
  <p>Now you can store them at -20°C or transform in your favorite strain. </p>
+
-
  <div align="right"><small><a href="#indice">^top</a></small></div>
+
-
  <p><br />
+
-
    <br />
+
-
  </p>
+
-
  <h1> <span class="mw-headline" id="PCR">PCR</span></h1>
+
-
  <ul>
+
-
    <li>For every DNA sample you want to amplify, put:
+
-
      <ul>
+
-
        <li>2 µl buffer </li>
+
-
        <li>0.6 µl MgCl2 </li>
+
-
        <li>0.4 µl dNTPs </li>
+
-
        <li>1 µl DNA (or ddH2O for blank sample). If you are performing a colony PCR, pick up the desired colony from a plate with a tip and dip it in the solution. </li>
+
-
        <li>0.25 µl Taq Polymerase </li>
+
-
        <li>0.5 ul VF2 primer (10 uM) </li>
+
-
        <li>0.5 ul VR primer (10 uM) </li>
+
-
        <li>A proper amount of ddH2O to have 20 µl of total reaction volume </li>
+
-
      </ul>
+
-
    </li>
+
-
    <li>into an eppendorf tube. </li>
+
-
    <li>Put the Eppendorf tube in the thermal cycler and set this program:
+
-
      <ul>
+
-
        <li>95°C 10 min </li>
+
-
        <li>CYCLE:
+
-
          <ul>
+
-
            <li>95°C 30 sec </li>
+
-
            <li>60°C 1 min </li>
+
-
            <li>72°C 1-3 min </li>
+
           </ul>
           </ul>
         </li>
         </li>
-
         <li>for 35 cycles </li>
+
         <li>Cast the gel, insert the well-forming comb and let it polymerize </li>
-
        <li>72°C 7 min </li>
+
        <li>Add the loading buffer (10x Blue Juice, Invitrogen) to each sample </li>
-
        <li>16°C forever. </li>
+
        <li>Load the samples and 8 µl of marker (when not specified: 1 kb Plus DNA Ladder, Fermentas) </li>
-
      </ul>
+
        <li>Set to 70-100 volts and electrophorese for the required amount of time </li>
-
    </li>
+
        <li>Use UV-light to look at the bands (using gloves and protective glasses) </li>
-
    <li>Now you can add a loading buffer to the solution and perform electrophoresis to check the amplified sequence length. </li>
+
        <li>Take a picture of the gel, if needed (not when bands have to be cut!!!) </li>
-
  </ul>
+
      </ul></td>
-
  <div align="right"><small><a href="#indice">^top</a></small></div>
+
    <td valign="top"><div class="thumb tright">
-
  <p><br />
+
        <div class="thumbinner" style="width:182px;"><a href="/wiki/index.php?title=Special:Upload&amp;wpDestFile=1kb_unipv.jpg" class="new" title="File:1kb unipv.jpg">File:1kb unipv.jpg</a>
-
    <br />
+
          <div class="thumbcaption">1kb marker</div>
-
  </p>
+
        </div>
-
  <h1> <span class="mw-headline" id="Electrophoresis">Electrophoresis</span></h1>
+
      </div></td>
-
  <table>
+
  </tr>
-
    <tr>
+
</table>
-
      <td valign="top"><ul>
+
<h2> <span class="mw-headline" id="1_kb_Plus_DNA_Ladder_preparation_.28Fermentas.29">1 kb Plus DNA Ladder preparation (Fermentas)</span></h2>
-
          <li>Prepare agarose gel in 1x TBE buffer </li>
+
<p>Mix gently: </p>
-
          <li>Add ethidium bromide (using gloves and face mask for your safety):
+
<ul>
-
            <ul>
+
  <li>1ul of DNA ladder (1 kb) </li>
-
              <li>1,5 µl in the small size agarose gel (70 ml) </li>
+
  <li>1ul of 6X DNA Loading Dye </li>
-
              <li>3 µl in the middle size agarose gel (150 ml) </li>
+
  <li>4ul of Deionizied water </li>
-
              <li>5 µl in the big size agarose gel (250 ml) </li>
+
</ul>
-
            </ul>
+
<p>A final volume of 6ul to load </p>
-
          </li>
+
<div align="right"><small><a href="#indice">^top</a></small></div>
-
          <li>Cast the gel, insert the well-forming comb and let it polymerize </li>
+
<p><br />
-
          <li>Add the loading buffer (10x Blue Juice, Invitrogen) to each sample </li>
+
  <br />
-
          <li>Load the samples and 8 µl of marker (when not specified: 1 kb Plus DNA Ladder, Fermentas) </li>
+
</p>
-
          <li>Set to 70-100 volts and electrophorese for the required amount of time </li>
+
<h1> <span class="mw-headline" id="Glycerol_stocks">Glycerol stocks</span></h1>
-
          <li>Use UV-light to look at the bands (using gloves and protective glasses) </li>
+
<ul>
-
          <li>Take a picture of the gel, if needed (not when bands have to be cut!!!) </li>
+
  <li>Mix 750 ul from the 5 ml sample of the incubated bacteria with 250 ul of 80% glycerol </li>
-
        </ul></td>
+
  <li>Leave at -20°C for one day </li>
-
      <td valign="top"><div class="thumb tright">
+
  <li>Move to -80°C the day after </li>
-
          <div class="thumbinner" style="width:182px;"><a href="/wiki/index.php?title=Special:Upload&amp;wpDestFile=1kb_unipv.jpg" class="new" title="File:1kb unipv.jpg">File:1kb unipv.jpg</a>
+
</ul>
-
            <div class="thumbcaption">1kb marker</div>
+
<div align="right"><small><a href="#indice">^top</a></small></div>
-
          </div>
+
<p><br />
-
        </div></td>
+
  <br />
-
    </tr>
+
</p>
-
  </table>
+
<h1> <span class="mw-headline" id="X-Gal_staining_protocol_for_beta_galactosidase_.28blue.2Fwhite_screening.29">X-Gal staining protocol for beta galactosidase (blue/white screening)</span></h1>
-
  <h2> <span class="mw-headline" id="1_kb_Plus_DNA_Ladder_preparation_.28Fermentas.29">1 kb Plus DNA Ladder preparation (Fermentas)</span></h2>
+
<ul>
-
  <p>Mix gently: </p>
+
  <li>The principle is that X-Gal (5-bromo-4-chloro-3-indolyl-b-D-galactopyranoside) turns blue when reacts with beta-galactosidase. </li>
-
  <ul>
+
  <li>Mix 20 ul X-Gal 40 mg/ml and 60 ul LB and spread on required LB agar plates (X-Gal and DMF are toxic, use face-mask for your safety!!! X-Gal is light-sensitive, remember to keep it in the dark, when possible). </li>
-
    <li>1ul of DNA ladder (1 kb) </li>
+
  <li>If you have to induce beta-galactosidase production (for example in lac operon) add 20 ul of IPTG 200 mM to the mix. </li>
-
    <li>1ul of 6X DNA Loading Dye </li>
+
  <li>Let plates dry at 37°C and than plate bacteria. </li>
-
    <li>4ul of Deionizied water </li>
+
  <li>Incubate at 37°C. </li>
-
  </ul>
+
  <li>Result: blue colonies express LacZ, while white colonies don't. </li>
-
  <p>A final volume of 6ul to load </p>
+
</ul>
-
  <div align="right"><small><a href="#indice">^top</a></small></div>
+
<div align="right"><small><a href="#indice">^top</a></small></div>
-
  <p><br />
+
<p><br />
-
    <br />
+
  <br />
-
  </p>
+
</p>
-
  <h1> <span class="mw-headline" id="Glycerol_stocks">Glycerol stocks</span></h1>
+
<h1> <span class="mw-headline" id="Sudan_Black_staining_protocol">Sudan Black staining protocol</span></h1>
-
  <ul>
+
<ul>
-
    <li>Mix 750 ul from the 5 ml sample of the incubated bacteria with 250 ul of 80% glycerol </li>
+
  <li>Take 70 ul of colture and spread it onto a slide. </li>
-
    <li>Leave at -20°C for one day </li>
+
  <li>Allow the smear on the slide to dry. </li>
-
    <li>Move to -80°C the day after </li>
+
  <li>Heat fix the slide by passing it through a Bunsen burner flame. </li>
-
  </ul>
+
  <li>Place a few drops of Sudan Black solution (0,3% in 70% ethanol) on the fixed preparation. </li>
-
  <div align="right"><small><a href="#indice">^top</a></small></div>
+
  <li>Leave the solution work for 10 minutes till the ethanol in the stain is evaporated. </li>
-
  <p><br />
+
  <li>Immerse the slide in the xylene for 10 seconds to allow the decolorization. </li>
-
    <br />
+
  <li>Add Safranine solution (0,5% in wather) to the slide and leave it for 10 seconds to allow the counter-staining. </li>
-
  </p>
+
  <li>Wash the slide with running water. </li>
-
  <h1> <span class="mw-headline" id="X-Gal_staining_protocol_for_beta_galactosidase_.28blue.2Fwhite_screening.29">X-Gal staining protocol for beta galactosidase (blue/white screening)</span></h1>
+
  <li>When the slide is completely dry, add a drop of immersion oil directly to the slide. </li>
-
  <ul>
+
  <li>Examine the slide with optical microscope with 100x oil immersion objective. </li>
-
    <li>The principle is that X-Gal (5-bromo-4-chloro-3-indolyl-b-D-galactopyranoside) turns blue when reacts with beta-galactosidase. </li>
+
</ul>
-
    <li>Mix 20 ul X-Gal 40 mg/ml and 60 ul LB and spread on required LB agar plates (X-Gal and DMF are toxic, use face-mask for your safety!!! X-Gal is light-sensitive, remember to keep it in the dark, when possible). </li>
+
<div align="right"><small><a href="#indice">^top</a></small></div>
-
    <li>If you have to induce beta-galactosidase production (for example in lac operon) add 20 ul of IPTG 200 mM to the mix. </li>
+
<p><br />
-
    <li>Let plates dry at 37°C and than plate bacteria. </li>
+
  <br />
-
    <li>Incubate at 37°C. </li>
+
</p>
-
    <li>Result: blue colonies express LacZ, while white colonies don't. </li>
+
<h1> <span class="mw-headline" id="Yeast_cultures">Yeast cultures</span></h1>
-
  </ul>
+
<h2> <span class="mw-headline" id="Liquid_YPD_medium_.280.5_L.29">Liquid YPD medium (0.5 L)</span></h2>
-
  <div align="right"><small><a href="#indice">^top</a></small></div>
+
<ul>
-
  <p><br />
+
  <li>5 g yeast extract </li>
-
    <br />
+
  <li>10 g peptone </li>
-
  </p>
+
  <li>450 ml ddH2O </li>
-
  <h1> <span class="mw-headline" id="Sudan_Black_staining_protocol">Sudan Black staining protocol</span></h1>
+
  <li>Autoclave </li>
-
  <ul>
+
  <li>Add 50 ml of 20% glucose to reach the final concentration of 2% </li>
-
    <li>Take 70 ul of colture and spread it onto a slide. </li>
+
  <li>Add 2 ml of G418 geneticin (50 mg/ml stock) at the final concentration of 200 ug/ml </li>
-
    <li>Allow the smear on the slide to dry. </li>
+
</ul>
-
    <li>Heat fix the slide by passing it through a Bunsen burner flame. </li>
+
<div align="right"><small><a href="#indice">^top</a></small></div>
-
    <li>Place a few drops of Sudan Black solution (0,3% in 70% ethanol) on the fixed preparation. </li>
+
<h2> <span class="mw-headline" id="YPD_agar_.280.5_L.29">YPD agar (0.5 L)</span></h2>
-
    <li>Leave the solution work for 10 minutes till the ethanol in the stain is evaporated. </li>
+
<ul>
-
    <li>Immerse the slide in the xylene for 10 seconds to allow the decolorization. </li>
+
  <li>5 g yeast extract </li>
-
    <li>Add Safranine solution (0,5% in wather) to the slide and leave it for 10 seconds to allow the counter-staining. </li>
+
  <li>10 g peptone </li>
-
    <li>Wash the slide with running water. </li>
+
  <li>10 g agar </li>
-
    <li>When the slide is completely dry, add a drop of immersion oil directly to the slide. </li>
+
  <li>450 ml ddH2O </li>
-
    <li>Examine the slide with optical microscope with 100x oil immersion objective. </li>
+
  <li>Autoclave </li>
-
  </ul>
+
  <li>Add 50 ml of 20% glucose to reach the final concentration of 2% </li>
-
  <div align="right"><small><a href="#indice">^top</a></small></div>
+
  <li>Add 2 ml of G418 geneticin (50 mg/ml stock) at the final concentration of 200 ug/ml </li>
-
  <p><br />
+
</ul>
-
    <br />
+
<div align="right"><small><a href="#indice">^top</a></small></div>
-
  </p>
+
<h2> <span class="mw-headline" id="G418_stock_solution_.2850_mg.2Fml.29">G418 stock solution (50 mg/ml)</span></h2>
-
  <h1> <span class="mw-headline" id="Yeast_cultures">Yeast cultures</span></h1>
+
<ul>
-
  <h2> <span class="mw-headline" id="Liquid_YPD_medium_.280.5_L.29">Liquid YPD medium (0.5 L)</span></h2>
+
  <li>Add 20 ml of ddH2O to 1 g of G418 powder (Sigma) </li>
-
  <ul>
+
  <li>Filter-sterilize (0.2 um) and aliquot in 1 ml stocks </li>
-
    <li>5 g yeast extract </li>
+
  <li>Store at +4°C as recommended by Sigma </li>
-
    <li>10 g peptone </li>
+
</ul>
-
    <li>450 ml ddH2O </li>
+
<div align="right"><small><a href="#indice">^top</a></small></div>
-
    <li>Autoclave </li>
+
<h2> <span class="mw-headline" id="LiAc_1M">LiAc 1M</span></h2>
-
    <li>Add 50 ml of 20% glucose to reach the final concentration of 2% </li>
+
<ul>
-
    <li>Add 2 ml of G418 geneticin (50 mg/ml stock) at the final concentration of 200 ug/ml </li>
+
  <li>Dissolve 1 g of LiAc dihydrate (Sigma) in ddH2O to a final volume of 10 ml </li>
-
  </ul>
+
  <li>Filter-sterilize (0.2 um) and store at +4°C </li>
-
  <div align="right"><small><a href="#indice">^top</a></small></div>
+
</ul>
-
  <h2> <span class="mw-headline" id="YPD_agar_.280.5_L.29">YPD agar (0.5 L)</span></h2>
+
<div align="right"><small><a href="#indice">^top</a></small></div>
-
  <ul>
+
<h2> <span class="mw-headline" id="PEG_3350_50.25">PEG 3350 50%</span></h2>
-
    <li>5 g yeast extract </li>
+
<ul>
-
    <li>10 g peptone </li>
+
  <li>Dissolve 20 g of PEG 3350 (Sigma) in ddH2O on a magnetic stirrer to a final volume of 40 ml </li>
-
    <li>10 g agar </li>
+
  <li>Autoclave </li>
-
    <li>450 ml ddH2O </li>
+
  <li>Store at room temperature </li>
-
    <li>Autoclave </li>
+
</ul>
-
    <li>Add 50 ml of 20% glucose to reach the final concentration of 2% </li>
+
<div align="right"><small><a href="#indice">^top</a></small></div>
-
    <li>Add 2 ml of G418 geneticin (50 mg/ml stock) at the final concentration of 200 ug/ml </li>
+
<h2> <span class="mw-headline" id="Long_term_glycerol_stocks">Long term glycerol stocks</span></h2>
-
  </ul>
+
<ul>
-
  <div align="right"><small><a href="#indice">^top</a></small></div>
+
  <li>Mix 810 ul of an overnight yeast culture with 190 ul of sterile 80% glycerol </li>
-
  <h2> <span class="mw-headline" id="G418_stock_solution_.2850_mg.2Fml.29">G418 stock solution (50 mg/ml)</span></h2>
+
  <li>Vortex and store at -80°C </li>
-
  <ul>
+
</ul>
-
    <li>Add 20 ml of ddH2O to 1 g of G418 powder (Sigma) </li>
+
<div align="right"><small><a href="#indice">^top</a></small></div>
-
    <li>Filter-sterilize (0.2 um) and aliquot in 1 ml stocks </li>
+
<h2> <span class="mw-headline" id="Yeast_transformation">Yeast transformation</span></h2>
-
    <li>Store at +4°C as recommended by Sigma </li>
+
<ul>
-
  </ul>
+
  <li>Follow this protocol: <a href="http://openwetware.org/wiki/High_Efficiency_Transformation" class="external free" rel="nofollow">http://openwetware.org/wiki/High_Efficiency_Transformation</a> until "Pipette </li>
-
  <div align="right"><small><a href="#indice">^top</a></small></div>
+
</ul>
-
  <h2> <span class="mw-headline" id="LiAc_1M">LiAc 1M</span></h2>
+
<p>1.0 ml of sterile water into each tube; stir the pellet by with a micropipette tip and vortex" step. </p>
-
  <ul>
+
<ul>
-
    <li>Dissolve 1 g of LiAc dihydrate (Sigma) in ddH2O to a final volume of 10 ml </li>
+
  <li>Centrifuge at 3000g 5 min, remove the supernatant and inoculate the pellet in 1 ml of pre-warmed </li>
-
    <li>Filter-sterilize (0.2 um) and store at +4°C </li>
+
</ul>
-
  </ul>
+
<p>YPD in a 15 ml falcon tube. </p>
-
  <div align="right"><small><a href="#indice">^top</a></small></div>
+
<ul>
-
  <h2> <span class="mw-headline" id="PEG_3350_50.25">PEG 3350 50%</span></h2>
+
  <li>Incubate the cultures at 30°C, 200rpm for 2h. </li>
-
  <ul>
+
  <li>Centrifuge at 3000g 5 min, remove the supernatant and resuspend the pellet in the remaining </li>
-
    <li>Dissolve 20 g of PEG 3350 (Sigma) in ddH2O on a magnetic stirrer to a final volume of 40 ml </li>
+
</ul>
-
    <li>Autoclave </li>
+
<p>YPD. </p>
-
    <li>Store at room temperature </li>
+
<ul>
-
  </ul>
+
  <li>Plate the whole cells on a G418 plate, pre-incubated at room temperature. </li>
-
  <div align="right"><small><a href="#indice">^top</a></small></div>
+
  <li>Incubate the plated cells at 28-30°C until colonies appear. </li>
-
  <h2> <span class="mw-headline" id="Long_term_glycerol_stocks">Long term glycerol stocks</span></h2>
+
</ul>
-
  <ul>
+
<p><br />
-
    <li>Mix 810 ul of an overnight yeast culture with 190 ul of sterile 80% glycerol </li>
+
</p>
-
    <li>Vortex and store at -80°C </li>
+
<div align="right"><small><a href="#indice">^top</a></small></div>
-
  </ul>
+
<p><br />
-
  <div align="right"><small><a href="#indice">^top</a></small></div>
+
  <br />
-
  <h2> <span class="mw-headline" id="Yeast_transformation">Yeast transformation</span></h2>
+
</p>
-
  <ul>
+
-
    <li>Follow this protocol: <a href="http://openwetware.org/wiki/High_Efficiency_Transformation" class="external free" rel="nofollow">http://openwetware.org/wiki/High_Efficiency_Transformation</a> until "Pipette </li>
+
-
  </ul>
+
-
  <p>1.0 ml of sterile water into each tube; stir the pellet by with a micropipette tip and vortex" step. </p>
+
-
  <ul>
+
-
    <li>Centrifuge at 3000g 5 min, remove the supernatant and inoculate the pellet in 1 ml of pre-warmed </li>
+
-
  </ul>
+
-
  <p>YPD in a 15 ml falcon tube. </p>
+
-
  <ul>
+
-
    <li>Incubate the cultures at 30°C, 200rpm for 2h. </li>
+
-
    <li>Centrifuge at 3000g 5 min, remove the supernatant and resuspend the pellet in the remaining </li>
+
-
  </ul>
+
-
  <p>YPD. </p>
+
-
  <ul>
+
-
    <li>Plate the whole cells on a G418 plate, pre-incubated at room temperature. </li>
+
-
    <li>Incubate the plated cells at 28-30°C until colonies appear. </li>
+
-
  </ul>
+
-
  <p><br />
+
-
  </p>
+
-
  <div align="right"><small><a href="#indice">^top</a></small></div>
+
-
  <p><br />
+
-
    <br />
+
-
  </p>
+
-
 
+

Revision as of 12:39, 17 August 2011

UNIPV TEAM 2011

PROTOCOLS

PROTOCOLS



Contents

Media & Antibiotics

LB

  • Add:
    • 10 g/L NaCl
    • 10 g/L Bacto-Tryptone
    • 5 g/L Bacto-Yeast Extract
    • ddH2O
to a sterile pyrex bottle
  • autoclave
  • (add antibiotic when it reaches ~45°C)
  • store at +4°C


LB Agar

  • Add:
    • 10 g/L NaCl
    • 10 g/L Bacto-Tryptone
    • 5 g/L Bacto-Yeast Extract
    • 15 g/L Bacto-Agar
    • ddH2O

to a sterile 1L flask

  • autoclave
  • (add antibiotic when the agar becomes visible in the liquid, at about 45°C; shake gently to avoid bubbles)
  • pour into Petri plates and close them immediately
  • let them polymerize for ~2-3h
  • invert plates and wrap them with aluminium foil and store at +4°C


SOB

  • Add:
    • 5 g/L Bacto-Yeast Extract
    • 20 g/L Bacto-Tryptone
    • 10mM NaCl
    • 2.5mM KCl
    • 10mM MgSO4
    • 10mM MgCl2

to a sterile pyrex bottle

  • (optional: check that pH is ~6.8, otherwise adjust with NaOH)
  • autoclave
  • (add antibiotic when it reaches ~45°C)
  • store at +4°C


SOC

  • Prepare SOB and add 20 ml of 1M glucose (prepare it dissolving 3.6 g of glucose in 20 ml of ddH2O).


M9 supplemented with glycerol (M9gly)

For 1L of medium, add:

  • 734 ml of autoclaved (and cooled to Tamb, N.B. consider evaporation during autoclaving) ddH2O with a magnetic stirrer inside the bottle
  • 5 ml of autoclaved 80% glycerol as carbon source
  • 100 ul of autoclaved or filtered (0.2um) CaCl2 1 M
  • 20 ml of 10% autoclaved casamino acids (dissolve 50 g in 500 ml = 10% stock)
  • 34 ml of filtered (0.2um) thiamine hydrochloride MW=337.27g/mol (340 mg in 34 ml) (keep in mind it is photosensitive)
  • 2 ml of autoclaved MgSO4 1 M
  • 200 ml of autoclaved M9 salts 5x (dissolve 56.4 g in 1 liter ddH2O = 5x stock)
  • shake the ddH2O with the magnetic stirrer and start adding the other solutions in sterility (each solution must be completely dissolved!) in the order listed above.
  • add antibiotic if needed
  • store at +4°C, protected from light

NOTE:

  • M9 salts 5x, 10% casamino acids, MgSO4 1 M and CaCl2 1 M can be stored at +4°C.
  • glycerol 80% can be stored at room temperature.
  • thiamine hydrochloride (LIGHT SENSITIVE) is one-shot and must be prepared each time (keep in mind you loose some volume during filtration)



Antibiotics

Stocks at -20°C freezer:

  • Ampicillin 100 mg/ml (in water)
  • Kanamycin 50 mg/ml (in water)
  • Chloramphenicol 34 mg/ml (in 100% ethanol)

These stocks are 1000x for high copy number plasmids. For low copy number plasmids, you should use these final concentrations in media:

  • Ampicillin 50 ug/ml
  • Kanamycin 20 ug/ml
  • Chloramphenicol 12.5 ug/ml



E. coli transformation

Transforming home-made competent cells

  • heat ligation at 65°C to inactivate T4 ligase
  • thaw in ice a vial of TOP10 competent cells stored at -80°C
  • incubate a selective LB agar plate at 37°C
  • pipet 800ul of LB (without antibiotic) in a 15ml falcon tube and incubate it at 37°C
  • heat the water bath at 42°C


  • add 1 ul (~3ng of DNA vector) of ligation to 100ul of thawed TOP10
  • add parafilm and incubate in ice for 30 min
  • heat shock at 42°C for 1 min
  • incubate in ice for 2 min
  • transfer transformed bacteria to 800ul of pre-warmed LB
  • incubate at 37°C, 220 rpm for 1 h
  • centrifuge at 2000 rpm, 25°C for 10 min
  • take 750ul of supernatant and resuspend the pellet in the remaining LB (~150ul)
  • plate the entire culture and incubate the plate at 37°C overnight

Variants:

  • if you transform a miniprep, add less than 3 ng in order to have single colonies
  • if you use another home-made competent strain, the protocol is the same but you should consider the transformation efficiency to add a proper amount of DNA
  • if you use commercial Invitrogen TOP10 the protocol changes and it is reported below.



Transforming commercial competent cells

(according to manufacturer's protocol)

  • heat ligation at 65°C to inactivate T4 ligase
  • thaw in ice a vial of TOP10 competent cells stored at -80°C (one vial contains 50ul of cells)
  • incubate a selective LB agar plate at 37°C
  • heat the water bath at 42°C
  • dilute the ligation 1:50 (or 1:100) in ddH2O, in order to have less than 100pg/ul
  • add 1 ul of ligation (or less than 100pg of miniprepped DNA) to 25 or 50ul of thawed TOP10
  • add parafilm and incubate in ice for 10 min
  • heat shock at 42°C for 1 min
  • incubate in ice for 2 min
  • add 250ul of SOC medium
  • incubate at 37°C, 220 rpm for 1 h
  • plate 150ul of the culture and incubate the plate at 37°C overnight
  • the remaining 150ul can be stored at +4°C



E. coli competent cells preparation

H. Inoue et al. (1990), High efficiency transformation of Escherichia coli with plasmids, Gene 96 23-28.

DAY1
inoculum 5-8 ul from -80°C stock in 5 ml of LB (37°C, 220 rpm ON);
DAY2
dilution 1:1000 in SOB (flask, 18-25°C, 220 rpm ON);
DAY3
pre-chill centrifuge at 4°C;
prepare TB (prepare 50 ml every 125 ml of SOB):
  • 15mM CaCl2
  • 250mM KCl
  • 10mM (3 g/L) Pipes
  • adjust pH at 6.7 with KOH
  • 55mM (8.9 g/L) MnCl2
  • filter (0.2 um) the solution and chill in 50 ml
put the flask in ice when the culture reaches OD600=~0.05 (1mm pathlength – NanoDrop);
aliquot in pre-chilled 50 ml falcon tubes;
centrifuge at 2500g (4400rpm), 4°C, 10 min;
ICE: discard, resuspend in 40 ml of TB each 125 ml SOB, centrifuge as before;
ICE: discard, resuspend in 10 ml of TB each 125 ml SOB, add 700ul DMSO;
ICE: aliquot 100ul in pre-chilled 0.5ml tubes;
put in -80°C freezer;

ALWAYS TEST THE EFFICIENCY IN [CFU/ug] UNITS: transform 100ul of competent cells with 4ng of DNA and 100ul of competent cells without DNA (add 1ul of ddH2O), then plate on proper LB agar plates.

This protocol has shown to work with:

  • DH5alpha (10^8 with 100ul of cells);
  • TOP10 (5*10^7 with 100ul of cells);
  • BW20767 (10^3 with 100ul of cells);
  • DB3.1 (5*10^4 with 100ul of cells);



J. Sambrook, E.F. Fritsch, T. Maniatis (1989)

  • DAY1
    • Inoculum 5-8 ul from -80°C stock in 5 ml of LB (37°C, 220 rpm ON).
  • DAY2
    • Dilution 1:500 in LB (flask, 30-37°C, 220 rpm), monitor OD600 until it reaches 0.04 (1mm pathlength – NanoDrop, it should take from 3 to 5 hours);
    • prepare the proper amount of 50 ml tubes in ice and pre-chill the centrifuge;
    • when the culture reaches the right OD600, aliquot the culture in the pre-chilled tubes;
    • centrifuge (4000rpm, 4°C, 10min) and discard the supernatant;
    • for each 50 ml of culture, add 30 ml of MgCl2-CaCl2 solution (Buffer1) and resuspend the pellet;
    • centrifuge (4000rpm, 4°C, 10min) and discard the supernatant;
    • for each 50 ml of the original culture, add 2 ml of CaCl2 solution (Buffer2) and resuspend the pellet;
    • aliquot in 0.5 ml tubes and store at -80°C.

ALWAYS TEST THE EFFICIENCY IN [CFU/ug] UNITS

Buffers preparation
  • Buffer1: 80mM MgCl2, 20mM CaCl2 (e.g.: mix 8 ml MgCl2 1M, 2 ml CaCl2 1M and 90 ml ddH2O):
    • put ddH2O into a flask or a bottle and autoclave it;
    • add MgCl2 previously filter-sterilized (0,2 um) and CaCl2 previously autoclaved or filter-sterilized (0,2 um).
  • Buffer2: 0.1 M CaCl2 and 15% of glycerol (e.g.: mix 100 mL of 1M CaCl2, 150 mL of 100% Glycerol and 750 mL of ddH2O):
    • put ddH2O and glycerol into a flask and autoclave it;
    • add CaCl2 previously autoclaved or filter-sterilized (0,2 um).

Keep Buffers cold.



E. coli strains (all in -80°C freezer)

TOP10

F- mcrA Δ(mrr-hsdRMS-mcrBC) φ80lacZΔM15 ΔlacX74 nupG recA1 araD139 Δ(ara-leu)7697 galE15 galK16 rpsL(StrR) endA1 λ-

  • competent cells already prepared (5*10^7 CFU/ug with100ul of cells)
  • competent cells from Invitrogen available (10^9 CFU/ug with 50ul of cells)
  • commonly used for cloning and expression in our lab
  • they are equal to DH10B strain, whose genome is available from NCBI

NOTE: they have

  • lacI wt
  • cI of phi80 prophage (different from cI of lambda phage)
  • Streptomycin resistance

DH5alpha

F- endA1 glnV44 thi-1 recA1 relA1 gyrA96 deoR nupG Φ80dlacZΔM15 Δ(lacZYA-argF)U169, hsdR17(rK- mK+), λ–

  • competent cells already prepared (10^8 CFU/ug with100ul of cells)
  • commonly used for cloning

BW20767

F-, RP4-2(Km::Tn7,Tc::Mu-1), leu-163::IS10, ΔuidA3::pir+, recA1, endA1, thi-1, hsdR17, creC510

  • competent cells already prepared (10^3 CFU/ug with100ul of cells)
  • not used for cloning

NOTE: they have

  • a fully working lac operon (already tested on IPTG/X-Gal plates)
  • Kan and Tet resistance (not tested)

XL1-Blue

endA1 gyrA96(nalR) thi-1 recA1 relA1 lac glnV44 F'[ ::Tn10 proAB+ lacIq Δ(lacZ)M15] hsdR17(rK- mK+)

  • competent cells never prepared
  • a small stock of competent cells is available
  • used for cloning

NOTE: they have lacIQ

DB3.1

F- gyrA462 endA1 glnV44 Δ(sr1-recA) mcrB mrr hsdS20(rB-, mB-) ara14 galK2 lacY1 proA2 rpsL20(Smr) xyl5 Δleu mtl1

  • competent cells already prepared (5*10^4 CFU/ug with 100ul of cells)
  • used for in vivo amplification of ccdB plasmids

NOTE: they have a working lacZ, but a deleted lacY, they become slightly blue on IPTG/X-Gal plates

STBL3

F- glnV44 recA13 mcrB mrr hsdS20(rB-, mB-) ara-14 galK2 lacY1 proA2 rpsL20 xyl-5 leu mtl-1

  • competent cells never prepared
  • used for in vivo amplification of DNA with direct repeats

NOTE: they cannot be used for blue/white screening

CW2553 + pJat8

Genotype: Khlebnikov A et al. (2000), Regulatable Arabinose-Inducible Gene Expression System with Consistent Control in All Cells of a Culture, Journal of Bacteriology, Vol. 182, No. 24, p.7029-7034.

  • pJat8 is Gentamycine resistant

NOTE:

  • the stock of this strain has been grown without Gen
  • this strain is used for araBAD inducible system

MG1655 (seq)

F-, λ-, rph-1

  • CGSC#7740
  • Fully sequenced genome (GenBank: NC_000913)

MC1061

F-, Δ(araA-leu)7697, [araD139]B/r, Δ(codB-lacI)3, galK16, galE15(GalS), λ-, e14-, mcrA0, relA1, rpsL150(strR), spoT1, mcrB1, hsdR2

  • CGSC#6649

BW25141

F-, Δ(araD-araB)567, ΔlacZ4787(::rrnB-3), Δ(phoB-phoR)580, λ-, galU95, ΔuidA3::pir+, recA1, endA9(del-ins)::FRT, rph-1, Δ(rhaD-rhaB)568, hsdR514

  • CGSC#7635
  • Carry the wild type pir gene

BW25142

F-, Δ(araD-araB)567, ΔlacZ4787(::rrnB-3), Δ(phoB-phoR)580, λ-, galU95, ΔuidA4::pir-116, recA1, endA9(del-ins)::FRT, rph-1, Δ(rhaD-rhaB)568, hsdR514

  • CGSC#6649
  • Carry the pir-116 gene

BW23473

F-, Δ(argF-lac)169, ΔuidA3::pir+, recA1, rpoS396(Am)?, endA9(del-ins)::FRT?, rph-1, hsdR514, rob-1, creC510

  • CGSC#7837
  • Carry the wild type pir gene

BW23474

F-, Δ(argF-lac)169, ΔuidA4::pir-116, recA1, rpoS396(Am)?, endA9(del-ins)::FRT, rph-1, hsdR514, rob-1, creC510

  • CGSC#7838
  • Carry the pir-116 gene



Long term bacterial glycerol stocks

  • Mix 750 ul of a culture (preferably in log-phase) with 250 ul of 80% glycerol, in a 1.5ml vial
  • label the vial with name, date and antibiotic resistance
  • leave at -20°C for one day
  • move to -80°C the day after



Plasmid digestion for BioBrick Standard Assembly

To open vectors
  • a volume containing 1 ug of purified plasmid
  • 2.5 ul of 10X buffer H
  • 1 ul of first enzyme
  • 1 ul of second enzyme
  • 25 ul final volume
  • incubate at 37°C for 3 hours
To excide fragments
  • A volume containing 1-1.8 ug of purified plasmid
  • 2.5 ul of buffer H
  • 1 ul of first enzyme
  • 1 ul of second enzyme
  • 25 ul final volume
  • incubate at 37°C for 3 hours

NOTE: if you are performing a digestion for screening, 1 hour of incubation is sufficient.



Ethanol precipitation with sodium acetate

  • Add 1/10 DNA solution volume of sodium acetate 3 M, pH 5.2
  • Add 2.5 DNA solution volume of absolute ethanol
  • Freeze at -80°C for 30 min
  • Centrifuge at 13000 rpm, 4°C for 20 min
  • Decant supernatant
  • Add 250 µl of 70% ethanol
  • Centrifuge at 13000 rpm, 4°C for 20 min
  • Remove all supernatant with a pipette
  • Air dry pellet until ethanol is totally removed
  • Elute with 5-10 µl of ddH2O



Ligation

After the purification of two digested DNA fragments:

  • add a volume containing 20-50 ng of vector
  • add a volume containing:

File:Pv formula lig.png

("6" can be lowered to "2")

  • heat DNA mix at 65°C for 5 min for DNA denaturation
  • add 1 ul of T4 Ligase buffer (check if ATP is completely dissolved)
  • add 1 ul of T4 Ligase
  • 10-20 µl final volume
  • incubate at 16°C overnight
  • inactivate the T4 Ligase heating at 65°C for 10 min
  • then, ligation can be conserved at 4°C or can be transformed

NOTE: When the purified DNA of the insert also contains its native vector, you can perform the ligation anyway, but its antibiotic resistance must be different from the acceptor vector's resistance in order to select correct transformants on agar plates. When doing this, you should modify the ligation protocol:

  • you should use "2" or "3" instead of "6" to compute the insert mass;
  • when you add the volume containing the insert mass, you must consider that the DNA quantification with NanoDrop refers to insert+NATIVE VECTOR. So, you must add:

File:Pv formula lig 2.jpeg



DNA resuspension from iGEM plates

  • Find the right position of the DNA of interest in iGEM plates
  • Resuspend with 15 ul ddH2O and transfer it in 0,5 ml sterile Eppendorf tubes

Now you can store them at -20°C or transform in your favorite strain.



PCR

  • For every DNA sample you want to amplify, put:
    • 2 µl buffer
    • 0.6 µl MgCl2
    • 0.4 µl dNTPs
    • 1 µl DNA (or ddH2O for blank sample). If you are performing a colony PCR, pick up the desired colony from a plate with a tip and dip it in the solution.
    • 0.25 µl Taq Polymerase
    • 0.5 ul VF2 primer (10 uM)
    • 0.5 ul VR primer (10 uM)
    • A proper amount of ddH2O to have 20 µl of total reaction volume
  • into an eppendorf tube.
  • Put the Eppendorf tube in the thermal cycler and set this program:
    • 95°C 10 min
    • CYCLE:
      • 95°C 30 sec
      • 60°C 1 min
      • 72°C 1-3 min
    • for 35 cycles
    • 72°C 7 min
    • 16°C forever.
  • Now you can add a loading buffer to the solution and perform electrophoresis to check the amplified sequence length.



Electrophoresis

  • Prepare agarose gel in 1x TBE buffer
  • Add ethidium bromide (using gloves and face mask for your safety):
    • 1,5 µl in the small size agarose gel (70 ml)
    • 3 µl in the middle size agarose gel (150 ml)
    • 5 µl in the big size agarose gel (250 ml)
  • Cast the gel, insert the well-forming comb and let it polymerize
  • Add the loading buffer (10x Blue Juice, Invitrogen) to each sample
  • Load the samples and 8 µl of marker (when not specified: 1 kb Plus DNA Ladder, Fermentas)
  • Set to 70-100 volts and electrophorese for the required amount of time
  • Use UV-light to look at the bands (using gloves and protective glasses)
  • Take a picture of the gel, if needed (not when bands have to be cut!!!)
File:1kb unipv.jpg
1kb marker

1 kb Plus DNA Ladder preparation (Fermentas)

Mix gently:

  • 1ul of DNA ladder (1 kb)
  • 1ul of 6X DNA Loading Dye
  • 4ul of Deionizied water

A final volume of 6ul to load



Glycerol stocks

  • Mix 750 ul from the 5 ml sample of the incubated bacteria with 250 ul of 80% glycerol
  • Leave at -20°C for one day
  • Move to -80°C the day after



X-Gal staining protocol for beta galactosidase (blue/white screening)

  • The principle is that X-Gal (5-bromo-4-chloro-3-indolyl-b-D-galactopyranoside) turns blue when reacts with beta-galactosidase.
  • Mix 20 ul X-Gal 40 mg/ml and 60 ul LB and spread on required LB agar plates (X-Gal and DMF are toxic, use face-mask for your safety!!! X-Gal is light-sensitive, remember to keep it in the dark, when possible).
  • If you have to induce beta-galactosidase production (for example in lac operon) add 20 ul of IPTG 200 mM to the mix.
  • Let plates dry at 37°C and than plate bacteria.
  • Incubate at 37°C.
  • Result: blue colonies express LacZ, while white colonies don't.



Sudan Black staining protocol

  • Take 70 ul of colture and spread it onto a slide.
  • Allow the smear on the slide to dry.
  • Heat fix the slide by passing it through a Bunsen burner flame.
  • Place a few drops of Sudan Black solution (0,3% in 70% ethanol) on the fixed preparation.
  • Leave the solution work for 10 minutes till the ethanol in the stain is evaporated.
  • Immerse the slide in the xylene for 10 seconds to allow the decolorization.
  • Add Safranine solution (0,5% in wather) to the slide and leave it for 10 seconds to allow the counter-staining.
  • Wash the slide with running water.
  • When the slide is completely dry, add a drop of immersion oil directly to the slide.
  • Examine the slide with optical microscope with 100x oil immersion objective.



Yeast cultures

Liquid YPD medium (0.5 L)

  • 5 g yeast extract
  • 10 g peptone
  • 450 ml ddH2O
  • Autoclave
  • Add 50 ml of 20% glucose to reach the final concentration of 2%
  • Add 2 ml of G418 geneticin (50 mg/ml stock) at the final concentration of 200 ug/ml

YPD agar (0.5 L)

  • 5 g yeast extract
  • 10 g peptone
  • 10 g agar
  • 450 ml ddH2O
  • Autoclave
  • Add 50 ml of 20% glucose to reach the final concentration of 2%
  • Add 2 ml of G418 geneticin (50 mg/ml stock) at the final concentration of 200 ug/ml

G418 stock solution (50 mg/ml)

  • Add 20 ml of ddH2O to 1 g of G418 powder (Sigma)
  • Filter-sterilize (0.2 um) and aliquot in 1 ml stocks
  • Store at +4°C as recommended by Sigma

LiAc 1M

  • Dissolve 1 g of LiAc dihydrate (Sigma) in ddH2O to a final volume of 10 ml
  • Filter-sterilize (0.2 um) and store at +4°C

PEG 3350 50%

  • Dissolve 20 g of PEG 3350 (Sigma) in ddH2O on a magnetic stirrer to a final volume of 40 ml
  • Autoclave
  • Store at room temperature

Long term glycerol stocks

  • Mix 810 ul of an overnight yeast culture with 190 ul of sterile 80% glycerol
  • Vortex and store at -80°C

Yeast transformation

1.0 ml of sterile water into each tube; stir the pellet by with a micropipette tip and vortex" step.

  • Centrifuge at 3000g 5 min, remove the supernatant and inoculate the pellet in 1 ml of pre-warmed

YPD in a 15 ml falcon tube.

  • Incubate the cultures at 30°C, 200rpm for 2h.
  • Centrifuge at 3000g 5 min, remove the supernatant and resuspend the pellet in the remaining

YPD.

  • Plate the whole cells on a G418 plate, pre-incubated at room temperature.
  • Incubate the plated cells at 28-30°C until colonies appear.




Laboratory for Biomedical Informatics | Centre of Tissutal Engineering

University of Pavia
Retrieved from "http://2011.igem.org/Team:UNIPV-Pavia/Protocols"