Difference between revisions of "Team:Paris Saclay/Notebook/August/12"

(Dreamtaq PCR on puc19, detection, FRB, FKBP, SgRnaST, SgRnaNM and 1.2)
(PCR of pPS16_009)
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A Dreamtaq PCR was performed on pPS16_009 using the usual [[Team:Paris_Saclay/Experiments#taqPCR|protocol]].
 
A Dreamtaq PCR was performed on pPS16_009 using the usual [[Team:Paris_Saclay/Experiments#taqPCR|protocol]].
 
Primers: IPS83 ans IPS84
 
Primers: IPS83 ans IPS84
 +
 +
[[File:T--Paris_Saclay--120826_visualization_PCRGFP.jpeg|400px|thumb|right|Electrophoresis of PCR products, using primers IPS 83 and IPS 84 on pPS16_016.]]
  
 
====Extraction of puc19====
 
====Extraction of puc19====

Revision as of 14:29, 16 August 2016

Friday 12th August

Lab work

Visualization

PCR of pPS16_009

By Léa

A Dreamtaq PCR was performed on pPS16_009 using the usual protocol. Primers: IPS83 ans IPS84

File:T--Paris Saclay--120826 visualization PCRGFP.jpeg
Electrophoresis of PCR products, using primers IPS 83 and IPS 84 on pPS16_016.

Extraction of puc19

By Charlène

Clones 1 and 2 of puc19 were extracted with the Plasmid MiniPrep kit.

They were fast digested with EcoRI : 3µL of plasmid + 1µL of FD buffer + 0.5µL of FD EcoRI + 5.5µL of water, 15 minutes at 37°C.


Dreamtaq PCR on puc19, detection, FRB, FKBP, SgRNAst, SgRNAnm and gBlock 1.2

By Naiane, Mahnaz and Terrence

A Dreamtaq PCR was performed on puc19, detection, FRB, FKBP, SgRNAst, SgRNAnm and gBlock 1.2 using the usual protocol with these volumes :

Components Volume
10X DreamTaq Green Buffer 2.5µL
dNTP (10mM) 1µL
Primers mix (10µM each) 1µL
DreamTaq DNA polymerase 0.25µL
Nuclease-free water up to 25µL
Total volume 25µL

We made 6 clones of each colonie except for Puc19 where we made 1 negative control.