Team:Fatih Turkey/Procedures
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<a href="https://2011.igem.org/Team:Fatih_Turkey/Human_Practice">Human Practice</a> | <a href="https://2011.igem.org/Team:Fatih_Turkey/Human_Practice">Human Practice</a> | ||
<ul> | <ul> | ||
- | <li><a href="https://2011.igem.org/Team:Fatih_Turkey/Sporocide"> | + | <li><a href="https://2011.igem.org/Team:Fatih_Turkey/Sporocide">Sporicide</a></li> |
<li><a href="https://2011.igem.org/Team:Fatih_Turkey/iGEM_for_7_to_77">iGEM for 7 to 77</a></li> | <li><a href="https://2011.igem.org/Team:Fatih_Turkey/iGEM_for_7_to_77">iGEM for 7 to 77</a></li> | ||
<li><a href="https://2011.igem.org/Team:Fatih_Turkey/game">Game</a></li> | <li><a href="https://2011.igem.org/Team:Fatih_Turkey/game">Game</a></li> | ||
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<li><a | <li><a | ||
href="https://2011.igem.org/Team:Fatih_Turkey/Safety">Safety</a></li> | href="https://2011.igem.org/Team:Fatih_Turkey/Safety">Safety</a></li> | ||
+ | <li><a href="https://2011.igem.org/Team:Fatih_Turkey/collaboration">Collaboration</a></li> | ||
</ul> | </ul> | ||
</li> | </li> | ||
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<div class="bar-title-whole"> | <div class="bar-title-whole"> | ||
<div class="bar-title"> | <div class="bar-title"> | ||
- | <h2 style="font-family: Verdana, Arial, SunSans-Regular, sans-serif;"> | + | <h2 style="font-family: Verdana, Arial, SunSans-Regular, sans-serif;">Procedures</h2> |
- | <h5 style="font-family: Verdana, Arial, SunSans-Regular, sans-serif;"> | + | <h5 style="font-family: Verdana, Arial, SunSans-Regular, sans-serif;">E.coli Compotent</h5> |
</div> | </div> | ||
<div class="bar-title-sh-left"></div> | <div class="bar-title-sh-left"></div> | ||
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<div style="float: left; width: 220px; border-radius: 10px; position: absolute; top: 50px; left: 0; background: #EEE; border: solid 3px #666;"> | <div style="float: left; width: 220px; border-radius: 10px; position: absolute; top: 50px; left: 0; background: #EEE; border: solid 3px #666;"> | ||
<ol> | <ol> | ||
- | <li type="A"><a href="https://2011.igem.org/Team:Fatih_Turkey/ | + | <li type="A"><a href="https://2011.igem.org/Team:Fatih_Turkey/ecolicompetent">E.coli Competent</a> |
</li> | </li> | ||
- | <li type="A"><a href="https://2011.igem.org/Team:Fatih_Turkey/ | + | <li type="A"><a href="https://2011.igem.org/Team:Fatih_Turkey/ecolitransformation">E.coli Trasformation</a></li> |
- | <li type="A"><a href="https://2011.igem.org/Team:Fatih_Turkey/ | + | <li type="A"><a href="https://2011.igem.org/Team:Fatih_Turkey/bsubtilis">B.subtilis transformation</a></li> |
+ | <li type="A"><a href="https://2011.igem.org/Team:Fatih_Turkey/sporicideprocedure">Sporicide</a></li> | ||
</ol> | </ol> | ||
</div> | </div> | ||
<div style="width: 654px; border: solid 3px #666; border-radius: 10px; padding-left: 80px; margin-left: 170px;"> | <div style="width: 654px; border: solid 3px #666; border-radius: 10px; padding-left: 80px; margin-left: 170px;"> | ||
- | <p> | + | <div> |
+ | <div class="style1"> | ||
+ | <p>E.coli TOP10 Competent Cell</p> | ||
+ | </div> | ||
+ | <p class="style1">MATERIALS</p> | ||
+ | <p class="style1">· Centrifuge</p> | ||
+ | <p class="style1">· Autoclave</p> | ||
+ | <p class="style1">· Incubator with shaker</p> | ||
+ | <p class="style1">· pH meter</p> | ||
+ | <p class="style1">· Stock competent cell</p> | ||
+ | <p class="style1">· LB broth</p> | ||
+ | <p class="style1">· Falcon</p> | ||
+ | <p class="style1">· Ice</p> | ||
+ | <p class="style1">· Liquid nitrogen</p> | ||
+ | <p class="style1">· Bacto yeast extract</p> | ||
+ | <p class="style1">· Bacto tryptone</p> | ||
+ | <p class="style1">· Magnesium sulfate</p> | ||
+ | <p class="style1">· Potassium hydroxide</p> | ||
+ | <p class="style1">· Potassium acetate</p> | ||
+ | <p class="style1">· Rubidium chloride</p> | ||
+ | <p class="style1">· Calcium chloride</p> | ||
+ | <p class="style1">· Manganese chloride</p> | ||
+ | <p class="style1">· Glycerol</p> | ||
+ | <p class="style1">· Dilute acetic acid</p> | ||
+ | <p class="style1">· Filter</p> | ||
+ | <p class="style1">· MOPS</p> | ||
+ | <p class="style1">· Dilute NAOH</p> | ||
+ | <p class="style1">SOLUTIONS</p> | ||
+ | <p class="style1"><br /> | ||
+ | Preparation of Psi broth (per liter)<br /> | ||
+ | - 5 g bacto yeast extract<br /> | ||
+ | - 20 g bacto tryptone<br /> | ||
+ | - 5 g magnesium sulfate<br /> | ||
+ | - PH 7.6 with potassium hydroxide <br /> | ||
+ | - Autoclave 40 min<br /> | ||
+ | <br /> | ||
+ | Preparation of TfbI (per 200 ml)<br /> | ||
+ | - 0.588 g potassium acetate (final molarity/conc= 30 mM)<br /> | ||
+ | - 2.42 g rubidium chloride (final molarity/conc= 100 mM)<br /> | ||
+ | - 0.294 g calcium chloride (final molarity/conc= 10 mM)<br /> | ||
+ | - 2.0 g manganese chloride (final molarity/conc= 50 mM)<br /> | ||
+ | - 30 mL glycerol (15% v/v)<br /> | ||
+ | - Adjust PH 5.8 with dilute acetic acid<br /> | ||
+ | - Sterilize with filter <br /> | ||
+ | <br /> | ||
+ | Preparation of TfbII (per 100 ml)<br /> | ||
+ | - 0.21 g MOPS (final molarity/conc= 10 mM)<br /> | ||
+ | - 1.1 g calcium chloride (final molarity/conc= 75 mM)<br /> | ||
+ | - 0.121 g rubidium chloride (final molarity/conc= 10 mM)<br /> | ||
+ | - 15 mL glycerol (15% v/v)<br /> | ||
+ | <strong>- </strong>Adjust PH 6.5 with dilute NaOH <br /> | ||
+ | <strong>- </strong>Sterilize with filter</p> | ||
+ | <p class="style1">- Inoculate streak plates from liquid stock competent cells and incubate overnight at 37˚C </p> | ||
+ | <p class="style1">- Put 10 mL LB + colony into 50ml falcon. Incubate overnight at 37˚C with shaker</p> | ||
+ | <p class="style1">- Inoculate 200 ul to 1000 ul from overnight culture into 100-500 ml Psi broth (scale up or down as needed). Incubate at 37 C with aeration to A600=0.6-0.7 </p> | ||
+ | <p class="style1">- Ice 15 min. From this step onward the cells must remain <strong>COLD.</strong> (4C or on ice)<br /> | ||
+ | - Pellet cells in appropriate centrifuge tube 3-5000 x g 5 min (~5000 rpm in a Sorvall SS-34 rotor)<br /> | ||
+ | - Discard supernatant and add 0.4 volume (ie of original volume, here it is 40-400 ml) TfbI, resuspend and ice 15 min.<br /> | ||
+ | - Pellet cells in appropriate centrifuge tube 3-5000 x g 5 min (~5000 rpm in a Sorvall SS-34 rotor)<br /> | ||
+ | - Discard supernatant and resuspend in 0.04 volume TfbII, ice 15 min and either use immediately or quick freeze at -70C for storage. I usually save these in 100ul to 200ul aliquots. Quick freeze in ethanol-dry ice or liquid nitrogen prior to storage in a -70 to -80 C freezer. Thaw on ice just before using in a transformation experiment.</p> | ||
</div> | </div> | ||
</div> | </div> |
Latest revision as of 19:51, 28 October 2011
E.coli TOP10 Competent Cell
MATERIALS
· Centrifuge
· Autoclave
· Incubator with shaker
· pH meter
· Stock competent cell
· LB broth
· Falcon
· Ice
· Liquid nitrogen
· Bacto yeast extract
· Bacto tryptone
· Magnesium sulfate
· Potassium hydroxide
· Potassium acetate
· Rubidium chloride
· Calcium chloride
· Manganese chloride
· Glycerol
· Dilute acetic acid
· Filter
· MOPS
· Dilute NAOH
SOLUTIONS
Preparation of Psi broth (per liter)
- 5 g bacto yeast extract
- 20 g bacto tryptone
- 5 g magnesium sulfate
- PH 7.6 with potassium hydroxide
- Autoclave 40 min
Preparation of TfbI (per 200 ml)
- 0.588 g potassium acetate (final molarity/conc= 30 mM)
- 2.42 g rubidium chloride (final molarity/conc= 100 mM)
- 0.294 g calcium chloride (final molarity/conc= 10 mM)
- 2.0 g manganese chloride (final molarity/conc= 50 mM)
- 30 mL glycerol (15% v/v)
- Adjust PH 5.8 with dilute acetic acid
- Sterilize with filter
Preparation of TfbII (per 100 ml)
- 0.21 g MOPS (final molarity/conc= 10 mM)
- 1.1 g calcium chloride (final molarity/conc= 75 mM)
- 0.121 g rubidium chloride (final molarity/conc= 10 mM)
- 15 mL glycerol (15% v/v)
- Adjust PH 6.5 with dilute NaOH
- Sterilize with filter
- Inoculate streak plates from liquid stock competent cells and incubate overnight at 37˚C
- Put 10 mL LB + colony into 50ml falcon. Incubate overnight at 37˚C with shaker
- Inoculate 200 ul to 1000 ul from overnight culture into 100-500 ml Psi broth (scale up or down as needed). Incubate at 37 C with aeration to A600=0.6-0.7
- Ice 15 min. From this step onward the cells must remain COLD. (4C or on ice)
- Pellet cells in appropriate centrifuge tube 3-5000 x g 5 min (~5000 rpm in a Sorvall SS-34 rotor)
- Discard supernatant and add 0.4 volume (ie of original volume, here it is 40-400 ml) TfbI, resuspend and ice 15 min.
- Pellet cells in appropriate centrifuge tube 3-5000 x g 5 min (~5000 rpm in a Sorvall SS-34 rotor)
- Discard supernatant and resuspend in 0.04 volume TfbII, ice 15 min and either use immediately or quick freeze at -70C for storage. I usually save these in 100ul to 200ul aliquots. Quick freeze in ethanol-dry ice or liquid nitrogen prior to storage in a -70 to -80 C freezer. Thaw on ice just before using in a transformation experiment.