Team:Cambridge/Labwork/Protocols

From 2011.igem.org

(Difference between revisions)
m (Protocols)
Line 4: Line 4:
A list of all protocols developed during the project. To add one, use the section below.
A list of all protocols developed during the project. To add one, use the section below.
-
'''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.
Line 47: Line 47:
*[[Team:Cambridge/Protocols/Inclusion_Body_Prep | Inclusion Body Prep]] : A method to solubilise recombinant reflectin when it has been expressed in inclusion bodies in E. coli.
*[[Team:Cambridge/Protocols/Inclusion_Body_Prep | Inclusion Body Prep]] : A method to solubilise recombinant reflectin when it has been expressed in inclusion bodies in E. coli.
*[[Team:Cambridge/Protocols/Protein_Purification | His-Trap Protein Purification]] : A method to purify reflectin from E. coli lysate using a his-trap column.
*[[Team:Cambridge/Protocols/Protein_Purification | His-Trap Protein Purification]] : A method to purify reflectin from E. coli lysate using a his-trap column.
-
 
+
[[Team:Cambridge/Protocols/Norgen_Inclusion_Body_Prep |Norgen Inclusion Body Prep]] : A proprietary kit for      isolation of bacterial inclusion bodies
'''Protein Purification'''
'''Protein Purification'''
*[[Team:Cambridge/Protocols/Acetone_Precipitation_of_Proteins | Acetone Precipitation of proteins]] : A method to concentrate solutions of protein.
*[[Team:Cambridge/Protocols/Acetone_Precipitation_of_Proteins | Acetone Precipitation of proteins]] : A method to concentrate solutions of protein.

Revision as of 11:10, 16 September 2011

Loading...
OVERVIEW
home

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.

Norgen Inclusion Body Prep : A proprietary kit for isolation of bacterial inclusion bodies 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