Difference between revisions of "Team:Paris Saclay/Notebook/August/5"

(PCR Clean-up with the NucleoSpin kit)
(Lab work)
 
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{{Team:Paris_Saclay/notebook_header}}
 
{{Team:Paris_Saclay/notebook_header}}
= Friday 5<sup>st</sup> August=
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= Friday 5<sup>th</sup> August=
==Lab work==
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===Visualization===
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===Bringing DNA Closer===
 
==== DNA Extraction of DS-TDcasN- and DS-SPcasN-  ====
 
==== DNA Extraction of DS-TDcasN- and DS-SPcasN-  ====
 
''By Laetitia''
 
''By Laetitia''
 
  
 
The extraction was performed using the ChargeSwitc-Pro MiniPrep kit from Invitrogen. We followed this [[Team:Paris_Saclay/Experiments#DNA_extraction_using_the_Invitrogen_ChargeSwitch.C2.AE-Pro_Plasmid_Miniprep_Kit|protocol]].
 
The extraction was performed using the ChargeSwitc-Pro MiniPrep kit from Invitrogen. We followed this [[Team:Paris_Saclay/Experiments#DNA_extraction_using_the_Invitrogen_ChargeSwitch.C2.AE-Pro_Plasmid_Miniprep_Kit|protocol]].
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The extraction was performed on clone 11 for NM and clone 9 for 1.1 using the ChargeSwitc-Pro MiniPrep kit from Invitrogen. We followed this [[Team:Paris_Saclay/Experiments#DNA_extraction_using_the_Invitrogen_ChargeSwitch.C2.AE-Pro_Plasmid_Miniprep_Kit|protocol]].
 
The extraction was performed on clone 11 for NM and clone 9 for 1.1 using the ChargeSwitc-Pro MiniPrep kit from Invitrogen. We followed this [[Team:Paris_Saclay/Experiments#DNA_extraction_using_the_Invitrogen_ChargeSwitch.C2.AE-Pro_Plasmid_Miniprep_Kit|protocol]].
  
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===Visualization===
 
==== Q5 PCR on pPS16_003, pPS16_004, pPS16_006 and pPS16_007 ====
 
==== Q5 PCR on pPS16_003, pPS16_004, pPS16_006 and pPS16_007 ====
 
''By Caroline''
 
''By Caroline''
  
 
The PCR was carried out following the usual [[Team:Paris_Saclay/Experiments#Q5PCR|protocol]] adapted to 50µL and with a TM at 70°C. The specific [[Team:Paris_Saclay/Experiments#primers|primers]] for each parts were used. The products were put for migration on a 0.8%agarose gel with BET. Only, PCR form pPS16_003 and pPS16_004 showed a positive result.
 
The PCR was carried out following the usual [[Team:Paris_Saclay/Experiments#Q5PCR|protocol]] adapted to 50µL and with a TM at 70°C. The specific [[Team:Paris_Saclay/Experiments#primers|primers]] for each parts were used. The products were put for migration on a 0.8%agarose gel with BET. Only, PCR form pPS16_003 and pPS16_004 showed a positive result.
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[[File:T--Paris Saclay--160805 gel pcr.JPG|400px|thumb|right|Result of the PCR]]
  
 
==== PCR Clean-up with the NucleoSpin kit ====
 
==== PCR Clean-up with the NucleoSpin kit ====
 
''By Caroline''
 
''By Caroline''
  
The purification was carried out on PCR products 2.1, 2.2 and 4.1 following the usual [[Team:Paris_Saclay/Experiments#Purification|protocol]]. But, I forgot to dilute the Buffer NT3 with 100mL ethanol before I began the purification and so there was no DNA observed on the 0.8% agarose gel.
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The purification was carried out on PCR products 2.1 and 2.2 following the usual [[Team:Paris_Saclay/Experiments#Purification|protocol]].
 
+
  
 
File:T--Paris_Saclay--160722_Visualisation_PCRpPS16_002_7.JPG
 
File:T--Paris_Saclay--160722_Visualisation_PCRpPS16_002_7.JPG
  
 
{{Team:Paris_Saclay/notebook_footer}}
 
{{Team:Paris_Saclay/notebook_footer}}

Latest revision as of 16:21, 9 October 2016

Friday 5th August

Bringing DNA Closer

DNA Extraction of DS-TDcasN- and DS-SPcasN-

By Laetitia

The extraction was performed using the ChargeSwitc-Pro MiniPrep kit from Invitrogen. We followed this protocol.

The initial culture was at 20 mL so we increased (*4) the volumes until the precipitation.

Hence we used:

  • 1 ml of resuspension buffer
  • 1 ml lysis buffer
  • 1 ml precipitation buffer

The colum was used several times in order to recover the maximum of DNA

DNA Extraction of DS-NMcasN- and pPS_001

By Mathilde

The extraction was performed on clone 11 for NM and clone 9 for 1.1 using the ChargeSwitc-Pro MiniPrep kit from Invitrogen. We followed this protocol.

Visualization

Q5 PCR on pPS16_003, pPS16_004, pPS16_006 and pPS16_007

By Caroline

The PCR was carried out following the usual protocol adapted to 50µL and with a TM at 70°C. The specific primers for each parts were used. The products were put for migration on a 0.8%agarose gel with BET. Only, PCR form pPS16_003 and pPS16_004 showed a positive result.


Result of the PCR

PCR Clean-up with the NucleoSpin kit

By Caroline

The purification was carried out on PCR products 2.1 and 2.2 following the usual protocol.

File:T--Paris_Saclay--160722_Visualisation_PCRpPS16_002_7.JPG