Team:TU Darmstadt/Notebook/Methods/Heat shock transformation

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<ul class="menu"><li class="first"><a href="https://2014.igem.org/Team:TU_Darmstadt" >Home</a></li><li><a href="https://2014.igem.org/Team:TU_Darmstadt/Project" >Project</a></li><li><a href="https://2014.igem.org/Team:TU_Darmstadt/Results" >Results</a></li><li><a href="https://2014.igem.org/Team:TU_Darmstadt/PolicyandPractices" >Policy & Practices</a></li><li><a href="https://2014.igem.org/Team:TU_Darmstadt/Achievements" >Achievements</a></li><li class="active"><a href="https://2014.igem.org/Team:TU_Darmstadt/Notebook" >Notebook</a><ul class="menu2"><li class="first"><a href="https://2014.igem.org/Team:TU_Darmstadt/Notebook/Labjournal" >Labjournal</a></li><li><a href="https://2014.igem.org/Team:TU_Darmstadt/Notebook/Materials" >Materials</a></li><li class="active last"><a href="https://2014.igem.org/Team:TU_Darmstadt/Notebook/Methods" >Methods</a><ul class="menu3"><li class="first"><a href="https://2014.igem.org/Team:TU_Darmstadt/Notebook/Methods/Agarose_gel_electrophoresis" >Agarose gel electrophoresis</a></li><li><a href="https://2014.igem.org/Team:TU_Darmstadt/Notebook/Methods/Dephosphorylation" >Dephosphorylation</a></li><li ><a href="https://2014.igem.org/Team:TU_Darmstadt/Notebook/Methods/DNA_ligation" >DNA ligation</a></li><li><a href="https://2014.igem.org/Team:TU_Darmstadt/Notebook/Methods/DNA_quantification_with_NanoDrop" >DNA quantification with NanoDrop</a></li><li><a href="https://2014.igem.org/Team:TU_Darmstadt/Notebook/Methods/PCR_purification" >PCR purification</a></li><li><a href="https://2014.igem.org/Team:TU_Darmstadt/Notebook/Methods/PCR_with_Pfu_polymerase" >PCR with Pfu polymerase</a></li><li><a href="https://2014.igem.org/Team:TU_Darmstadt/Notebook/Methods/Plasmid_preparation" >Plasmid preparation</a></li ><li><a href="https://2014.igem.org/Team:TU_Darmstadt/Notebook/Methods/Restriction_digest" >Restriction digest</a></li><li><a href="https://2014.igem.org/Team:TU_Darmstadt/Notebook/Methods/SDS-PAGE" >SDS-PAGE</a></li><li><a href="https://2014.igem.org/Team:TU_Darmstadt/Notebook/Methods/Bacterial_cell_culture" >Bacterial cell culture</a></li><li ><a href="https://2014.igem.org/Team:TU_Darmstadt/Notebook/Methods/Cell_counting_plating" >Cell counting/plating</a></li><li ><a href="https://2014.igem.org/Team:TU_Darmstadt/Notebook/Methods/Chemically_competent_cells" >Chemically competent cells</a></li><li ><a href="https://2014.igem.org/Team:TU_Darmstadt/Notebook/Methods/Colony_PCR_with_Taq_polymerase" >Colony PCR with Taq polymerase</a></li><li><a href="https://2014.igem.org/Team:TU_Darmstadt/Notebook/Methods/Glycerine_stocks" >Glycerine stocks</a></li><li class="active"><a href="https://2014.igem.org/Team:TU_Darmstadt/Notebook/Methods/Heat_shock_transformation" >Heat shock transformation</a></li><li><a href="https://2014.igem.org/Team:TU_Darmstadt/Notebook/Methods/Protein expression" >Protein expression</a></li><li><a href="https://2014.igem.org/Team:TU_Darmstadt/Notebook/Methods/hydrochloric_acid_extraction" >37% hydrochloric acid extraction</a></li><li><a href="https://2014.igem.org/Team:TU_Darmstadt/Notebook/Methods/Dichloromethane_extraction" >Dichloromethane extraction</a></li><li><a href="https://2014.igem.org/Team:TU_Darmstadt/Notebook/Methods/Methanol_extraction" >Methanol extraction</a></li><li class="last"><a href="https://2014.igem.org/Team:TU_Darmstadt/Notebook/Methods/Ethanol_extraction" >Ethanol extraction</a></li></ul></li></ul></li><li><a href="https://2014.igem.org/Team:TU_Darmstadt/Team" >Team</a></li><li class="last"><a href="https://2014.igem.org/Team:TU_Darmstadt/Gallery" >Gallery</a></li></ul>
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<!--TYPO3SEARCH_begin--><div id="c101" class="csc-default"><div class="csc-header csc-header-n1"><h1 class="csc-firstHeader">Heat shock transformation</h1></div><div><p><b>Equipment:</b></p></div><div><p>- Heating bath</p></div><div><p>- Incubator</p></div><div></div><div><p><b>Chemicals &amp; consumables:</b></p></div><div><p>- Ice</p></div><div><p>- Pipets + steril tips</p></div><div><p>- LB medium</p></div><div><p>- LB-Agar-Plates + antibiotics</p></div><div></div><div><p><b>Procedure:</b></p></div><div></div><div><p>Defrost stocks of competent cells (100 µL in 1.5 ml Eppendorf tube) on ice.</p></div><div><p>Add the DNA and incubate the suspension for 15 minutes on ice.</p></div><div><p>Heat shock is done by incubating the cells for 45 seconds at 42°C. Put samples back on ice for 2 min.</p></div><div><p>Add 1 mL of LB medium and incubate for 1 hour at 37°C in order to obtain antibiotic resistance.</p></div><div><p>It might be useful to spin down cells at 5000 rpm for 5 min. Resuspend pellet in 100 µL LB.</p></div><div><p>Finally the cells are ready to be spread out.&nbsp;</p></div></div><!--TYPO3SEARCH_end-->
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<!--TYPO3SEARCH_begin--><div id="c101" class="csc-default"><div class="csc-header csc-header-n1"><h1 class="csc-firstHeader">Heat Shock Transformation</h1></div><div><p><b>Equipment:</b></p></div><div><p>- Heating bath</p></div><div><p>- Incubator</p></div><div></div><div><p><b>Chemicals &amp; consumables:</b></p></div><div><p>- Ice</p></div><div><p>- Pipets + steril tips</p></div><div><p>- LB medium</p></div><div><p>- LB-Agar-Plates + antibiotics</p></div><div></div><div><p><b>Procedure:</b></p></div><div></div><div><p>- Defrost stocks of competent cells (100 µL in 1.5 ml Eppendorf tube) on ice.</p></div><div><p>- Add the DNA and incubate the suspension for 15 minutes on ice.</p></div><div><p>- Heat shock is done by incubating the cells for 45 seconds at 42°C. Put samples back on ice for 2 min.</p></div><div><p>- Add 1 mL of LB medium and incubate for 1 hour at 37°C in order to obtain antibiotic resistance.</p></div><div><p>- It might be useful to spin down cells at 5000 rpm for 5 min. Resuspend pellet in 100 µL LB.</p></div><div><p>Finally the cells are ready to be spread out.&nbsp;</p></div></div><!--TYPO3SEARCH_end-->
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Latest revision as of 00:47, 18 October 2014

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Heat Shock Transformation

Equipment:

- Heating bath

- Incubator

Chemicals & consumables:

- Ice

- Pipets + steril tips

- LB medium

- LB-Agar-Plates + antibiotics

Procedure:

- Defrost stocks of competent cells (100 µL in 1.5 ml Eppendorf tube) on ice.

- Add the DNA and incubate the suspension for 15 minutes on ice.

- Heat shock is done by incubating the cells for 45 seconds at 42°C. Put samples back on ice for 2 min.

- Add 1 mL of LB medium and incubate for 1 hour at 37°C in order to obtain antibiotic resistance.

- It might be useful to spin down cells at 5000 rpm for 5 min. Resuspend pellet in 100 µL LB.

Finally the cells are ready to be spread out.