Difference between revisions of "Team:Paris Saclay/Notebook/August/26"

(Friday 26th August)
(Friday 26th August)
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''By Mathilde''
 
''By Mathilde''
  
Ligation products pPS16-003 and pPS16_004 frome the [[https://2016.igem.org/Team:Paris_Saclay/Notebook/August/25#Visualization|day before]] were purificated according to the usual [[https://2016.igem.org/Team:Paris_Saclay/Experiments#Purification_:_PCR_clean-up_with_NucleoSpin_Gel_and_PCR_Clean-up|protocol]]
+
Ligation products pPS16-003 and pPS16_004 frome the [[Team:Paris_Saclay/Notebook/August/25#Visualization|day before]] were purificated according to the usual [[Team:Paris_Saclay/Experiments#Purification_:_PCR_clean-up_with_NucleoSpin_Gel_and_PCR_Clean-up|protocol]]
  
 
   
 
   

Revision as of 13:55, 10 September 2016


Friday 26th August

Lab work

Visualization

Purification of pPS16-003 and pPS16_004 ligation products

By Mathilde

Ligation products pPS16-003 and pPS16_004 frome the day before were purificated according to the usual protocol


Q5 high fidelity PCR of pPS16_003 - pPS16_004 ligation product

By Mathilde

The Q5 PCR was conducted following the exact same protocol than the 25/08/2016 on the ligation product from the day before.

Migration Results

The two bands are at the expected size (1860 pb), so the fragment 2 (16-003 and pPS16_004 ligation product) is purified.

Purification of fragments 1(16-001 + pPS16_002) and 2 (16-003 + pPS16_004)

By Mathilde

The purification was made following the usual [[1]]. Each of those purification products were quantified on nanodrop.

Segment DNA quantity (ng/µL) 260/230 260/280
1 2
84,20 1,25 1,84
169,88 1,29 1,83