Team:Paris Saclay/Notebook/July/3

From 2013.igem.org

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(Summary:)
(Summary:)
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=='''Summary:'''==
=='''Summary:'''==
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*Observed the Petri dish, we decided to perform a PCR test for the colonies from these 4 mediums.
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*From those incubated plates, 4 colonies (2 from FNR+plasmid PSB1C3, 2 from LacZ and AmilCP) were selected in parallel for further test.  
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*Continued what we started yesterday. Observed the Petri dish, selected the colonies. 4 colonies in total, they were 2 include FNR+plasmid in PSB1C3 and 2 from the control.  
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*Used 4 primers: VF2, VR, PFNR_up, PFNR_down for verification. They were designed to cut 4 special sites for creating 3 different regions on plasmid chain: VF2/VR, VF2/PFNR_down, PFNR_up/VR. The PCR products had been put on electrophoresis gel for the verification
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*Used 4 primers: VF2, VR, Pfnr_up, Pfnr_down for the verification test. They were designed to cut 4 special sites for creating 3 different regions on plasmid chain: VF2/VR, VF2/PFNR_down, PFNR_up/VR. After the amplification, those PCR products had been put on electrophoresis gel for the verification.
=='''Lab work'''==
=='''Lab work'''==

Revision as of 20:42, 10 September 2013

Notebook : July 3

Summary:

  • Continued what we started yesterday. Observed the Petri dish, selected the colonies. 4 colonies in total, they were 2 include FNR+plasmid in PSB1C3 and 2 from the control.
  • Used 4 primers: VF2, VR, Pfnr_up, Pfnr_down for the verification test. They were designed to cut 4 special sites for creating 3 different regions on plasmid chain: VF2/VR, VF2/PFNR_down, PFNR_up/VR. After the amplification, those PCR products had been put on electrophoresis gel for the verification.

Lab work

constructing



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