Difference between revisions of "Team:Paris Saclay/Notebook/July/9"

(Plasmid Rehydratation :)
(Wednesday 8th July)
Line 30: Line 30:
 
   
 
   
 
Plasmid with promotor: J23101  
 
Plasmid with promotor: J23101  
10uL of our plasmid with promotor
+
* 10µL of our plasmid with promotor
1uL SpeI
+
* 1µL SpeI
1uL PstI
+
* 1µL PstI
2uL buffer 10x FD
+
* 2µL buffer 10x FD
  
 
Plasmid with gene: COO40 and K115017
 
Plasmid with gene: COO40 and K115017
10uL of our plasmid with gene
+
* 10µL of our plasmid with gene
1uL XbaI
+
* 1µL XbaI
1uL PstI
+
* 1µL PstI
2uL buffer 10x FD
+
* 2µL buffer 10x FD
  
 
After this step, we separate the sequence we need from the sequence we don't with electrophoresis
 
After this step, we separate the sequence we need from the sequence we don't with electrophoresis
Line 46: Line 46:
 
''by Pauline and Audrey''
 
''by Pauline and Audrey''
  
Preparation of Agarose Gel 1%, 0,5g in 50mL of 1X TAE, 0,5uL of BET
+
Preparation of Agarose Gel 1%, 0,5g in 50mL of 1X TAE, 0,5µL of BET
 
Migration 0,06A 80V  
 
Migration 0,06A 80V  
  
Line 52: Line 52:
 
''by Pauline and Audrey''
 
''by Pauline and Audrey''
 
We quantify with the electrophoresis gel:
 
We quantify with the electrophoresis gel:
C0040: 10ng/uL
+
* C0040: 10ng/µL
J23101: 20ng/uL
+
* J23101: 20ng/µL
K115017: we don't see enough of fluorescent to quantify the biobrick. We decide to amplify this one by PCR.
+
* K115017: we don't see enough of fluorescent to quantify the biobrick. We decide to amplify this one by PCR.
  
 
'''Members present:'''
 
'''Members present:'''
 
* Instructors and advisors: Alice.
 
* Instructors and advisors: Alice.
 
* Students: Johan, Seong Koo, Audrey, Coralie, Pauline
 
* Students: Johan, Seong Koo, Audrey, Coralie, Pauline

Revision as of 10:45, 15 July 2015

Wednesday 8th July

Lab Work

Transformation

by Coralie

Ligation product:

  • J23101 + I13504
  • J23106 + I13504
  • J23117 + I13504

On LB + Ampicillin 100ug/mL Incubation ON, 37°C

"by Johan and Seong Koo"

R0051 On LB + Ampicillin 100ug/mL Incubation ON, 37°C

Plasmid Rehydratation :

by Johan and Audrey

Biobricks:

  • S03518
  • B0030
  • B0015
  • K1399005

Digestion

by Pauline and Audrey

Plasmid with promotor: J23101

  • 10µL of our plasmid with promotor
  • 1µL SpeI
  • 1µL PstI
  • 2µL buffer 10x FD

Plasmid with gene: COO40 and K115017

  • 10µL of our plasmid with gene
  • 1µL XbaI
  • 1µL PstI
  • 2µL buffer 10x FD

After this step, we separate the sequence we need from the sequence we don't with electrophoresis

Electrophoresis

by Pauline and Audrey

Preparation of Agarose Gel 1%, 0,5g in 50mL of 1X TAE, 0,5µL of BET Migration 0,06A 80V

Quantification

by Pauline and Audrey We quantify with the electrophoresis gel:

  • C0040: 10ng/µL
  • J23101: 20ng/µL
  • K115017: we don't see enough of fluorescent to quantify the biobrick. We decide to amplify this one by PCR.

Members present:

  • Instructors and advisors: Alice.
  • Students: Johan, Seong Koo, Audrey, Coralie, Pauline