Team:Cambridge/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. | ||
+ | * [[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. | ||
+ | * [[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/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. | ||
- | * [[Team:Cambridge/Protocols/MiniPrep|<u><span style="color:#00000CD">MiniPrep</span></u>]] A method used to extract DNA from bacterial cells. | + | * [[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. |
+ | * [[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. | ||
- | + | * [[Team:Cambridge/Protocols/SDSPAGE|<u><span style="color:#00000CD">SDS PAGE protein analysis</span></u>]] A method used to separate polypeptides of different lengths. | |
- | * [[Team:Cambridge/Protocols/SDSPAGE|<u><span style="color:#00000CD"> | + | |
* [[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
- Colony PCR PCR with cells as a template. Useful for checking the length of an insert in an introduced plasmid.
- Chemically competent cells generation A technique to produce e.coli cellsreceptive to chemical transformation.
- Electocompetent cells generation A technique to produce e.coli cells receptive to transformation by electroporation.
- Gel Electrophoresis A technique for separating DNA strands of different lengths.
- Gel Extraction of DNA A technique used to isolate a desired fragment of intact DNA from an agarose gel following agarose gel electrophoresis.
- Gibson Assembly A technique for ligating multiple DNA fragments in one step, compatible with standard assembly.
- LB Agar Plates preparation A method used to prepare agar plate to culture common bacteria.
- MiniPrep - DNA extraction A method used to extract DNA from bacterial cells.
- PCR using Phusion DNA polymerase A method for amplifying a section of DNA.
- SDS PAGE protein analysis A method used to separate polypeptides of different lengths.
- Restriction Enzyme Digest A method for creating a restriction map of a plasmid.
- Transformation of Bacillus subtilis A technique used to introduce foreign DNA into competent Bacillus cells.
- Transformation of Escherichia coli A method for transforming competent E.coli with DNA
N.B. Information in purple is subject to change through optimisation over the course of our project.
Lab supplies: [http://www.bioc.cam.ac.uk/stores/ BioPath Stores]