Team:Cambridge/Labwork/Protocols

From 2011.igem.org

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(Protocols)
(Protocols)
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'''Amplification of DNA'''
'''Amplification of DNA'''
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*[[Team:Cambridge/Protocols/PCR | Polymerase Chain Reaction]] : A method for amplifying a section of DNA
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*[[Team:Cambridge/Protocols/PCR | Polymerase Chain Reaction]] : A method for amplifying a section of DNA.
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*[[Team:Cambridge/Protocols/Colony PCR | Colony PCR]] : A method allowing to check the length of an insert in an introduced plasmid
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*[[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'''
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*[[Team:Cambridge/Protocols/Gel_Electrophoresis |Gel Electrophoresis]] : A method used to separate DNA fragments of different sizes
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*[[Team:Cambridge/Protocols/Gel_Electrophoresis |Gel Electrophoresis]] : A method used to separate DNA fragments of different sizes.
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*[[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
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*[[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.
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*[[Team:Cambridge/Protocols/Restriction_Enzyme_Digestion | Restriction Enzyme Digestion]] : A method for creating a restriction map of a plasmid
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*[[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.
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*[[Team:Cambridge/Protocols/Gibson_Assembly |Gibson Assembly]] : An extremely powerful technique for joining multiple arbitrary DNA sequences in one step, compatible with standard assembly.
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*[[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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OVERVIEW
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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

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

Bacterial Cultures

Extraction of DNA from Cells

Microscopy

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

Thin Film Preparation

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