Team:University of Ottawa/28 July 2008

From 2008.igem.org

(Difference between revisions)
(Today in the Lab)
 
(One intermediate revision not shown)
Line 92: Line 92:
</TABLE>
</TABLE>
::<li> Control for PCR Reaction was ddH2O instead of DNA template
::<li> Control for PCR Reaction was ddH2O instead of DNA template
 +
::<li> 12 PCR Reactions with identical DNA template
 +
'''Matt'''
 +
:'''PCR cleanup'''
 +
::<li> Performed a PCR cleanup of LiG ptp2/Pssa42
 +
:'''Transformation'''
 +
::<li> Transformed Ligated PTP2/pSSA42 into competent cells.
 +
:'''Inoculation'''
 +
::<li> Inoculated more pSSA42 vector for future digestion/ligations.

Latest revision as of 18:47, 7 August 2008

Untitled Document

 

 


Today in the Lab

Tammy and Dan

SampleConcentration 1 (ng/μL)V1 (μL)Concentration 2 (ng/μL)V2 (μL)H2O (μL)
T12375456056


  • PCR Amplification of T123
  • PCR Reaction components1X Vol (μl)13X Vol (μL)
    5X Reaction Buffer10 130
    10 mM each dNTP113
    F Primer (10 pmol/μL) F692.532.5
    R Primer (10 pmol/μL) F702.532.5
    DNA Template452
    Phusion Polymerase0.56.5
    Filtered Sterile ddH2O29.5383.5
  • Control for PCR Reaction was ddH2O instead of DNA template
  • 12 PCR Reactions with identical DNA template
  • Matt

    PCR cleanup
  • Performed a PCR cleanup of LiG ptp2/Pssa42
  • Transformation
  • Transformed Ligated PTP2/pSSA42 into competent cells.
  • Inoculation
  • Inoculated more pSSA42 vector for future digestion/ligations.