Team:Cambridge/Protocols

From 2012.igem.org

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* [[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/PCRcolony|Colony PCR]] 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/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/GelElectrophoresis|Gel Electrophoresis]] A technique for separating DNA strands of different lengths.  
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* [[Team:Cambridge/Protocols/GelElectrophoresis|<u><span style="color:#00000CD">Gel Electrophoresis</span></u>]] A technique for separating DNA strands of different lengths.  
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* [[Team:Cambridge/Protocols/GelExtractionofDNA|Gel Extraction of DNA]] 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/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/Gibsonassembly|Gibson Assembly]] A technique for ligating multiple DNA fragments in one step, compatible with standard assembly.
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* [[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/TransformationofE.coli| Transformation of ''Escherichia coli'']] A method for transforming competent ''E.coli'' with DNA
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* [[Team:Cambridge/Protocols/TransformationofE.coli|<u><span style="color:#00000CD">Transformation of ''Escherichia coli''</span></u> ]] A method for transforming competent ''E.coli'' with DNA
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* [[Team:Cambridge/Protocols/TransformationofB.subtilis|Transformation of ''Bacillus subtilis'']] A technique used to introduce foreign DNA into competent Bacillus cells.  
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* [[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.  
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* [[Team:Cambridge/Protocols/MiniPrep|MiniPrep]] A method used to extract DNA from bacterial cells.  
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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/RestrictionDigest| Restriction Enzyme Digest]] A method for creating a restriction map of a plasmid.
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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.
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* [[Team:Cambridge/Protocols/SDSPAGE| Protein analysis by SDS PAGE]] 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/Plates| Preparation of LB Agar Plates]] A method used to prepare agar plate to culture common bacteria.
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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.
'''N.B.''' Information in purple is subject to change through optimisation over the course of our project.
'''N.B.''' Information in purple is subject to change through optimisation over the course of our project.

Revision as of 23:07, 24 July 2012

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