Team:Cambridge/Experiments/Initial Exercise Group control

From 2011.igem.org

(Difference between revisions)
(PCR reaction)
(Construct Design)
Line 6: Line 6:
In the positive control experiment we replaced the Green Fluorescent Protein coding sequence with a coding sequence for mRUBY, which is a Bright Monomeric Red Fluorescent Protein.  
In the positive control experiment we replaced the Green Fluorescent Protein coding sequence with a coding sequence for mRUBY, which is a Bright Monomeric Red Fluorescent Protein.  
The picture below shows a map of the modified plasmid.  
The picture below shows a map of the modified plasmid.  
-
[[File:cam_plasmid_positivecontrol.jpg | middle | thumb | 400px | map of the modified plasmid with mRUBY insertion]]
+
File:cam_plasmid_positivecontrol.jpg | frameless | thumb | 600px | map of the modified plasmid with mRUBY insertion]]
===Experiment===
===Experiment===

Revision as of 10:54, 15 July 2011

Loading...
OVERVIEW
home

Contents

Positive Control Experiment

Construct Design

In the positive control experiment we replaced the Green Fluorescent Protein coding sequence with a coding sequence for mRUBY, which is a Bright Monomeric Red Fluorescent Protein. The picture below shows a map of the modified plasmid. File:cam_plasmid_positivecontrol.jpg | frameless | thumb | 600px | map of the modified plasmid with mRUBY insertion]]

Experiment

The experiment involved the same steps as preparation and expression of gene fusions of the three teams.

PCR reaction

  • We amplified the mRUBY coding sequence and two arms of the plasmid in a PCR reactions. First, we performed a real-time PCR with Taq polymerase, but as most samples were poorly amplified, we decided to repeat the reaction with Phusion polymerase (protocol)

The three reactions performed ae the following:

Reaction A
1μl primer ruby F (provided)
1μl primer ruby R (provided)
1μl mRuby template
Reaction B
1μl primer Vector F (provided)
1μl primer B reverse (provided)
1μl plasmid template
Reaction C
1μl primer Vector R (provided)
1μl primer A forward (provided)
1μl plasmid template
  • The graph presents accumulation of product with time in real-time PCR:
[[
progress of PCR reaction