Team:Cambridge/Labwork/Protocols
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'''Amplification of DNA''' | '''Amplification of DNA''' | ||
- | *[[Team:Cambridge/Protocols/PCR | Polymerase Chain Reaction]] : A method for amplifying a section of DNA | + | *[[Team:Cambridge/Protocols/PCR | Polymerase Chain Reaction]] : A method for amplifying a section of DNA. |
- | *[[Team:Cambridge/Protocols/Colony PCR | Colony PCR]] : | + | *[[Team:Cambridge/Protocols/Colony PCR | Colony PCR]] : PCR with cells as a template. Useful for checking the length of an insert in an introduced plasmid. |
'''Analysis of DNA''' | '''Analysis of DNA''' | ||
- | *[[Team:Cambridge/Protocols/Gel_Electrophoresis |Gel Electrophoresis]] : A method used to separate DNA fragments of different sizes | + | *[[Team:Cambridge/Protocols/Gel_Electrophoresis |Gel Electrophoresis]] : A method used to separate DNA fragments of different sizes. |
- | *[[Team:Cambridge/Protocols/Gel Extraction of DNA |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/Gel Extraction of DNA |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/DNA Precipitation |Rescue Precipitation of DNA]] : Creating a clean DNA solution after dissolving agarose gel. | *[[Team:Cambridge/Protocols/DNA Precipitation |Rescue Precipitation of DNA]] : Creating a clean DNA solution after dissolving agarose gel. | ||
- | *[[Team:Cambridge/Protocols/Restriction_Enzyme_Digestion | Restriction Enzyme Digestion]] : A method for creating a restriction map of a plasmid | + | *[[Team:Cambridge/Protocols/Restriction_Enzyme_Digestion | Restriction Enzyme Digestion]] : A method for creating a restriction map of a plasmid. |
'''Preparation of DNA Constructs''' | '''Preparation of DNA Constructs''' | ||
*[[Team:Cambridge/Protocols/Primer_design |Primer Design]] : Some general guidelines on how to design successful primers. | *[[Team:Cambridge/Protocols/Primer_design |Primer Design]] : Some general guidelines on how to design successful primers. | ||
- | *[[Team:Cambridge/Protocols/Gibson_Assembly |Gibson Assembly]] : An extremely powerful technique for joining multiple arbitrary DNA sequences in one step, compatible with standard assembly. | + | *[[Team:Cambridge/Protocols/Gibson_Assembly |Gibson Assembly]] : An extremely powerful technique for joining multiple, arbitrary DNA sequences in one step, compatible with standard assembly. |
'''Transformation of Bacterial Cells''' | '''Transformation of Bacterial Cells''' |
Revision as of 11:11, 14 September 2011
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Protocols
A list of all protocols developed during the project. To add one, use the section below.
Amplification of DNA
- Polymerase Chain Reaction : 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.
Analysis of DNA
- Gel Electrophoresis : A method used to separate DNA fragments of different sizes.
- Gel Extraction of DNA : A technique used to isolate a desired fragment of intact DNA from an agarose gel following agarose gel electrophoresis.
- Rescue Precipitation of DNA : Creating a clean DNA solution after dissolving agarose gel.
- Restriction Enzyme Digestion : A method for creating a restriction map of a plasmid.
Preparation of DNA Constructs
- Primer Design : Some general guidelines on how to design successful primers.
- Gibson Assembly : An extremely powerful technique for joining multiple, arbitrary DNA sequences in one step, compatible with standard assembly.
Transformation of Bacterial Cells
- Making Competent Cells : The methods required to make various cells competent
- Transformation of E.Coli : A simple method of transforming competent E.coli with your DNA of choice
- Tranformation of B. subtilis : A technique used to introduce foreign DNA into Bacillus cells.
- Transformation of E.coli by Electroporation: A technique for rapidly inserting DNA into cells, typically plasmid DNA, providing the cells are made competent in the correct manner.
Bacterial Cultures
- E. coli cell culture : A method for growing a cell culture in liquid medium
- Glycerol Stocks: A method of storing E.coli cells preserving their viability
Extraction of DNA from Cells
- Mini Prep : Extracting DNA from Bacterial Cells
- Extraction of genomic DNA from squid : A method to extract genomic DNA from squid tissue
- Extraction of cleaner genomic DNA from squid : A method to extract genomic DNA from squid tissue
Microscopy
- Confocal Microscopy : A method to visualise reflectins from squid samples.
- Slide Preparation for Confocal Microscopy : A method to perpare slides with agarose supplement to form microcolonies.
Protein Extraction
- Buffer Preparation : Methods to prepare the various buffers used to purify his-tagged reflectin from inclusion bodies in E. coli.
- Inclusion Body Prep : A method to solubilise recombinant reflectin when it has been expressed in inclusion bodies in E. coli.
- His-Trap Protein Purification : A method to purify reflectin from E. coli lysate using a his-trap column.
Protein Purification
- Acetone Precipitation of proteins : A method to concentrate solutions of protein.
- Ethanol Precipitation of proteins : A method to concentrate solutions of protein.
Thin Film Preparation
- Substrate Preparation:How to prepare a substrate for flow coating and spin coating.
- Spin Coating to Make a Thin Film: Our Spin Coating Protocol
- Flow Coating: How to flow coat a thin film.
Gel Electrophoresis by SDS PAGE
Adding new Protocols
To add a new protocol, enter the name in the box below and click new to create the new page. You must then return to this page in order to add in a link to the page by copying the code below.
Add a new link on this page with
#[[Team:Cambridge/Protocols/PROTOCOL_NAME_HERE |PROTOCOL NAME HERE]] : Insert description here