Difference between revisions of "Team:Paris Saclay/Notebook/July/22"

(Thursday 21th July)
(Visualization)
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===Visualization===
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====Low Fidelity Dreamtaq PCR of  transformed DH5α with pPS16_002====
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''By Mathilde''
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A DreamTaq PCR was made with [[Team:Paris_Saclay/Notebook/July/19#Visualization|transformed]] cultures  pPS16_002 following the usual [[Team:Paris_Saclay/Experiments#Polymerase_chain_reaction|protocol]] with Tm at 57°c and 5min for the initial denaturation.
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We divided up the PCR mix in  6 PCR tubes and added in each one a different clone from the transformed culture.
 +
The picked colonies were re-plated on a petri dish medium LB + Ampicillin (50µg/mL) + xGal/IPTG (1/1000).
 +
 
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Results :
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PCR products expected were :
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{| class="wikitable"
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|-
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!'''Plasmid'''
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!pPS16_002
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|-
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!'''Bande Size pb'''
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|960
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|}
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 +
 
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The electropheresis on agarose gel showed absolutely no PCR products. From this day, transformed culture from the 22/07/2016 will be used for the PCR experiments instead of those from the 19/07/2016.
 +
 
 +
 
  
  

Revision as of 13:28, 22 July 2016

Friday 22nd July

Lab work

Biobrick characterization

Low Fidelity Dreamtaq PCR of transformed DH5α with pPS16_002

By Mathilde

A DreamTaq PCR was made with transformed cultures pPS16_002 following the usual protocol with Tm at 57°c and 5min for the initial denaturation.

We divided up the PCR mix in 6 PCR tubes and added in each one a different clone from the transformed culture. The picked colonies were re-plated on a petri dish medium LB + Ampicillin (50µg/mL) + xGal/IPTG (1/1000).

Results : PCR products expected were :

Plasmid pPS16_002
Bande Size pb 960


The electropheresis on agarose gel showed absolutely no PCR products. From this day, transformed culture from the 22/07/2016 will be used for the PCR experiments instead of those from the 19/07/2016.