Team:Cambridge/Protocols

From 2012.igem.org

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(Protocols)
(Protocols)
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* [[Team:Cambridge/Protocols/PCRcolony|<u><span style="color:#00000CD">Colony PCR</span></u>]] PCR with cells as a template. Useful for checking the length of an insert in an introduced plasmid.
* [[Team:Cambridge/Protocols/PCRcolony|<u><span style="color:#00000CD">Colony PCR</span></u>]] PCR with cells as a template. Useful for checking the length of an insert in an introduced plasmid.
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* [[Team:Cambridge/Protocols/Chemicallycompetentcells|<u><span style="color:#00000CD">Chemically competent cells generation</span></u>]] A technique to produce e.coli cellsreceptive to chemical transformation.
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* [[Team:Cambridge/Protocols/Electrocompetentcells|<u><span style="color:#00000CD">Electocompetent cells generation</span></u>]] A technique to produce e.coli cells receptive to transformation by electroporation.
* [[Team:Cambridge/Protocols/GelElectrophoresis|<u><span style="color:#00000CD">Gel Electrophoresis</span></u>]] A technique for separating DNA strands of different lengths.  
* [[Team:Cambridge/Protocols/GelElectrophoresis|<u><span style="color:#00000CD">Gel Electrophoresis</span></u>]] A technique for separating DNA strands of different lengths.  
* [[Team:Cambridge/Protocols/GelExtractionofDNA|<u><span style="color:#00000CD">Gel Extraction of DNA</span></u>]] A technique used to isolate a desired fragment of intact DNA from an agarose gel following agarose gel electrophoresis.
* [[Team:Cambridge/Protocols/GelExtractionofDNA|<u><span style="color:#00000CD">Gel Extraction of DNA</span></u>]] A technique used to isolate a desired fragment of intact DNA from an agarose gel following agarose gel electrophoresis.
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* [[Team:Cambridge/Protocols/Electrocompetentcells|<u><span style="color:#00000CD">Generation of electocompetent cells</span></u>]] A technique to produce e.coli cells receptive to transformation by electroporation.
 
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* [[Team:Cambridge/Protocols/Chemicallycompetentcells|<u><span style="color:#00000CD">Generation of chemically competent cells</span></u>]] A technique to produce e.coli cellsreceptive to chemical transformation.
 
* [[Team:Cambridge/Protocols/Gibsonassembly|<u><span style="color:#00000CD">Gibson Assembly</span></u>]] A technique for ligating multiple DNA fragments in one step, compatible with standard assembly.
* [[Team:Cambridge/Protocols/Gibsonassembly|<u><span style="color:#00000CD">Gibson Assembly</span></u>]] A technique for ligating multiple DNA fragments in one step, compatible with standard assembly.
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* [[Team:Cambridge/Protocols/MiniPrep|<u><span style="color:#00000CD">MiniPrep</span></u>]] A method used to extract DNA from bacterial cells.
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* [[Team:Cambridge/Protocols/Plates|<u><span style="color:#00000CD">LB Agar Plates preparation</span></u>]] A method used to prepare agar plate to culture common bacteria.
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* [[Team:Cambridge/Protocols/MiniPrep|<u><span style="color:#00000CD">MiniPrep - DNA extraction</span></u>]] A method used to extract DNA from bacterial cells.
* [[Team:Cambridge/Protocols/PCRProtocol|<u><span style="color:#00000CD">PCR using Phusion DNA polymerase</span></u>]] A method for amplifying a section of DNA.  
* [[Team:Cambridge/Protocols/PCRProtocol|<u><span style="color:#00000CD">PCR using Phusion DNA polymerase</span></u>]] A method for amplifying a section of DNA.  
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* [[Team:Cambridge/Protocols/Plates|<u><span style="color:#00000CD">Preparation of LB Agar Plates</span></u>]] A method used to prepare agar plate to culture common bacteria.
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* [[Team:Cambridge/Protocols/SDSPAGE|<u><span style="color:#00000CD">SDS PAGE protein analysis</span></u>]] A method used to separate polypeptides of different lengths.
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* [[Team:Cambridge/Protocols/SDSPAGE|<u><span style="color:#00000CD">Protein analysis by SDS PAGE</span></u>]] A method used to separate polypeptides of different lengths.
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* [[Team:Cambridge/Protocols/RestrictionDigest|<u><span style="color:#00000CD">Restriction Enzyme Digest</span></u>]] A method for creating a restriction map of a plasmid.  
* [[Team:Cambridge/Protocols/RestrictionDigest|<u><span style="color:#00000CD">Restriction Enzyme Digest</span></u>]] A method for creating a restriction map of a plasmid.  
* [[Team:Cambridge/Protocols/TransformationofB.subtilis|<u><span style="color:#00000CD">Transformation of ''Bacillus subtilis''</span></u>]] A technique used to introduce foreign DNA into competent Bacillus cells.  
* [[Team:Cambridge/Protocols/TransformationofB.subtilis|<u><span style="color:#00000CD">Transformation of ''Bacillus subtilis''</span></u>]] A technique used to introduce foreign DNA into competent Bacillus cells.  

Revision as of 09:26, 8 August 2012

Protocols

N.B. Information in purple is subject to change through optimisation over the course of our project.


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