Team:Cambridge/Protocols
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=Protocols= | =Protocols= | ||
- | + | ===Construct production=== | |
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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/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. | ||
* [[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/PCRProtocol|<u><span style="color:#00000CD">PCR using a high temperature DNA polymerase</span></u>]] A method for amplifying a section of DNA. | * [[Team:Cambridge/Protocols/PCRProtocol|<u><span style="color:#00000CD">PCR using a high temperature DNA polymerase</span></u>]] A method for amplifying a section of DNA. | ||
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+ | ===Transformation protocols=== | ||
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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. | ||
+ | * [[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/ElectricalTransformation|<u><span style="color:#00000CD">Electroporation</span></u>]] A method for transforming appropriately competent cells with plasmid DNA using electricity. | ||
+ | * [[Team:Cambridge/Protocols/GlycerolStocks|<u><span style="color:#00000CD">Glycerol stocks</span></u>]] A technique for long term storage of cells at -80 degrees without losing cell vitality. | ||
* [[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. | ||
* [[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/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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+ | ===Construct verification=== | ||
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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/RestrictionDigest|<u><span style="color:#00000CD">Restriction Enzyme Digest</span></u>]] A method for creating a restriction map of a plasmid. | ||
+ | * [[Team:Cambridge/Protocols/MiniPrep|<u><span style="color:#00000CD">MiniPrep - DNA extraction</span></u>]] A method used to extract DNA from bacterial cells. | ||
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+ | ===Ribosense testing=== | ||
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+ | * [[Team:Cambridge/Protocols/beta-galactosidaseassay|<u><span style="color:#00000CD">β-galactosidase assay</span></u>]] Assay to measure the amount of the enzyme β-galactosidase being produced by a population of cells. Useful as a reporter system. | ||
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+ | ===Ratiometrica testing=== | ||
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+ | * [[Team:Cambridge/Protocols/IPTGInduction|<u><span style="color:#00000CD">IPTG induction</span></u>]] A technique for inducing the pSPANK promoter in E.coli cells. | ||
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+ | ===Miscellaneous=== | ||
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+ | * [[Team:Cambridge/Protocols/biobrick_protocols|<u><span style="color:#00000CD">BioBricks</span></u>]] Resources for manipulation of BioBricks and information regarding the distribution. | ||
+ | * [[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/SDSPAGE|<u><span style="color:#00000CD">SDS PAGE protein analysis</span></u>]] A method used to separate polypeptides of different lengths. | ||
==Recipes== | ==Recipes== |
Revision as of 10:44, 3 September 2012
Contents |
Protocols
Construct production
- 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.
- PCR using a high temperature DNA polymerase A method for amplifying a section of DNA.
Transformation protocols
- 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
- Electroporation A method for transforming appropriately competent cells with plasmid DNA using electricity.
- Glycerol stocks A technique for long term storage of cells at -80 degrees without losing cell vitality.
- 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
Construct verification
- Colony PCR PCR with cells as a template. Useful for checking the length of an insert in an introduced plasmid.
- Restriction Enzyme Digest A method for creating a restriction map of a plasmid.
- MiniPrep - DNA extraction A method used to extract DNA from bacterial cells.
Ribosense testing
- β-galactosidase assay Assay to measure the amount of the enzyme β-galactosidase being produced by a population of cells. Useful as a reporter system.
Ratiometrica testing
- IPTG induction A technique for inducing the pSPANK promoter in E.coli cells.
Miscellaneous
- BioBricks Resources for manipulation of BioBricks and information regarding the distribution.
- LB Agar Plates preparation A method used to prepare agar plate to culture common bacteria.
- SDS PAGE protein analysis A method used to separate polypeptides of different lengths.
Recipes
- CCMB80 for chemically competent cells generation A recipe for making CCMB80
- TAE buffer for gel electrophoresis A recipe for making 10xTAE buffer
- SOB growth medium A recipe for making SOB growth medium
Safety
See our Safety Page for Associated risk assessments for the above protocols and MSDS sheets for the reagents we have used.
Lab supplies
- [http://www.bioc.cam.ac.uk/stores/ BioPath Stores]
- [http://www.plantsci.cam.ac.uk/camonly/stores/stock.xls Plant Department Stores Catalogue xls (Updated 2nd July 2012)]
Other resources
File:Concentration calculator for lazy scientists.xls