Team:Cambridge/Protocols
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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. | ||
- | * [[Team:Cambridge/Protocols/PCRcolony|Colony PCR]] 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/GelElectrophoresis|Gel Electrophoresis]] 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|Gel Extraction of DNA]] 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. |
- | * [[Team:Cambridge/Protocols/Gibsonassembly|Gibson Assembly]] 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/TransformationofE.coli| Transformation of ''Escherichia coli'']] A method for transforming competent ''E.coli'' with DNA | + | * [[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 |
- | * [[Team:Cambridge/Protocols/TransformationofB.subtilis|Transformation of ''Bacillus subtilis'']] 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. |
- | * [[Team:Cambridge/Protocols/MiniPrep|MiniPrep]] A method used to extract DNA from bacterial cells. | + | * [[Team:Cambridge/Protocols/MiniPrep|<u><span style="color:#00000CD">MiniPrep</span></u>]] A method used to extract DNA from bacterial cells. |
- | * [[Team:Cambridge/Protocols/RestrictionDigest| Restriction Enzyme Digest]] 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/SDSPAGE| Protein analysis by SDS PAGE]] A method used to separate polypeptides of different lengths. | + | * [[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. |
- | * [[Team:Cambridge/Protocols/Plates| Preparation of LB Agar Plates]] A method used to prepare agar plate to culture common bacteria. | + | * [[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
- PCR using Phusion DNA polymerase A method for amplifying a section of DNA.
- Colony PCR PCR with cells as a template. Useful for checking the length of an insert in an introduced plasmid.
- 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.
- Transformation of Escherichia coli A method for transforming competent E.coli with DNA
- Transformation of Bacillus subtilis A technique used to introduce foreign DNA into competent Bacillus cells.
- MiniPrep A method used to extract DNA from bacterial cells.
- Restriction Enzyme Digest A method for creating a restriction map of a plasmid.
- Protein analysis by SDS PAGE A method used to separate polypeptides of different lengths.
- Preparation of LB Agar Plates 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.