Team:Kyoto/Protocol

From 2011.igem.org

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='''Protocol'''=
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<div id="main">
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Listed below our protocol for this project.<br>
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We hope you find them useful!!
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= '''Protocol''' =
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<html><a name="cloning"></a></html>
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=== Medium for drosophila ===
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[[File:Cloning.PNG|link=https://2011.igem.org/Team:Kyoto/Cloning|Cloning]]<br>
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::{| class="wikitable"
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[[File:Medium.PNG|link=https://2011.igem.org/Team:Kyoto/Medium|Medium]]<br>
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|+ [http://www.biol.se.tmu.ac.jp/fly/www/standard-medium.html Medium for drosophila]
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[[File:Measurement.PNG|link=https://2011.igem.org/Team:Kyoto/Measurement|Measurement]]
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! width="300" |Materials
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! width="300" |Methods
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* water : 500 mL
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* dry yeast : 20 g
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* corn flour : 45 g
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* glucose : 50 g
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* agarose : 3.5~5 g
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* propionic acid : 1.5 mL
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* 10 % p-hydroxybenzoate in 70 % Eternol : 5 g
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# Stir dry yeast and agarose with about two-thirds of water. Then, autoclave it.
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# Stir corn flour and glucose with the remaining water.
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# Stir 1 and 2, then autoclave it again.
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# after autoclave, add propionic acid and 10 % p-hydroxybenzoate in 70 % Eternol into it.■
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|}
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<br/>
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===M9 medium===
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::{| class="wikitable"
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! width="300" |Materials
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! width="300" |Methods
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* water : 1 L
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* Na2HPO4: 6 g
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* KH2PO4 : 3 g
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* NaCl : 0.5 g
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* NH4Cl : 1 g
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* 100 mM MgSO4 : 10 ml
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* 20 % glucose : 10 mL
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* 10 mM CaCl2 : 10 ml
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* 100 mM thiamine-HCl : 10 ml
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* 20 % casamino acid : 10 ml
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# Stir Na2HPO4, KH2PO4, NaCl and NH4Cl with water.
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# After autoclave, add 10 ml filter sterilized 100 mM MgSO4, 20 % glucose, 10 mM CaCl2, 100 mM thiamine-HCl.
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# If you need, add 10 ml filter sterilized 20 % casamino acid.
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|}
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<br/>
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===LB medium===
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::{| class="wikitable"
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! width="300" |Materials
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! width="300" |Methods
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* water : 1 L
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* Tryptone: 10 g
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* Yeast extract : 5 g
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* NaCl : 10 g
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* Agar : 15g
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# Stir Tryptone, Yeast extract and NaCl with water.
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# If you make LB plates, add agar.
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# Autoclave.
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|}
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<br/>
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===SOB medium===
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::{| class="wikitable"
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! width="300" |Materials
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! width="300" |Methods
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* water : 100 mL
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* Tryptone: 2 g
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* Yeast extract : 0.5 g
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* 5 M NaCl : 200 ul
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* 3 M KCl : 84 ul
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* 1 M MgSO4 : 1 ml
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* 1 M MgCl2 : 1 ml
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# Stir Tryptone and Yeast extract with water.
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# Add 200 ul 5 M NaCl and 84 ul 3 M KCl.
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# After autoclave, add 1 ml filter sterilized 10 mM MgSO4 and 10 mM MgCl2.
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|}
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<br/>
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===SOC medium===
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::{| class="wikitable"
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! width="300" |Materials
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! width="300" |Methods
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* SOB : 100 ml
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* 2 M glucose: 1 ml
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# Add 2 M glucose to 100 ml SOB.
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|}
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<br/>
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===Buffer TB===
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::{| class="wikitable"
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! width="300" |Materials
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! width="300" |Methods
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* water : 200 ml
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* PIPES : 3 g
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* CaCl2・2H2O : 0.22 g
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* 3 M KCl : 8.315 ml
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* KOH
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* MnCl2・4H2O : 1.09 g
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# Stir PIPES and CaCl2・2H2O with 100 ml water.
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# Add 8.315 ml 3 M KCl.
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# Add KOH and adjust pH 6.8.
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# Add MnCl2・4H2O.
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# Add water up to 200 ml.
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# Filter sterilize
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|}
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===DNS reaegnt===
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::{| class="wikitable"
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! width="300" |Materials
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! width="300" |Methods
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|-
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* 4.5% NaOH : 30 ml
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* 1% DNS : 88 ml
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* Rochelle salt : 25.5 g
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* 10% NaOH : 2.2 ml
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* Phenol : 1 g
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* Water : 7.8 ml
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* NaHCO3 : 0.69 g
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# Add 1% DNS 88ml and Rochelle salt 25.5 g to 4.5% NaOH (A solution)
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# Add Phenol 1 g and water 7.8 ml to 10% NaOH (B solution)
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# Add
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# Add
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# Add
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#
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|}
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</div>
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<!-- end of main -->
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Latest revision as of 02:26, 6 October 2011

Protocol

Listed below our protocol for this project.
We hope you find them useful!!

Cloning
Medium
Measurement

Retrieved from "http://2011.igem.org/Team:Kyoto/Protocol"