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

(Electrophoresis)
(Transformation)
Line 9: Line 9:
 
* BBa_J23106 + BBa_I13504
 
* BBa_J23106 + BBa_I13504
 
* BBa_J23117 + BBa_I13504
 
* BBa_J23117 + BBa_I13504
On LB + Ampicillin 100ug/mL.
+
On LB + Chloramphenicol 20ug/mL.
 
Incubation ON, 37°C
 
Incubation ON, 37°C
  

Revision as of 19:09, 13 September 2015


Thursday 9th July

Lab Work

Transformation

by Coralie

Ligation product:

  • BBa_J23101 + BBa_I13504
  • BBa_J23106 + BBa_I13504
  • BBa_J23117 + BBa_I13504

On LB + Chloramphenicol 20ug/mL. Incubation ON, 37°C

by Johan and Seong Ko

  • BBa_R0051

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

Plasmid Rehydratation

by Johan and Audrey

  • BBa_S03518
  • BBa_B0030
  • BBa_B0015
  • BBa_K1399005

Digestion

by Pauline and Audrey

Plasmid with promotor: BBa_J23101

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

Plasmid with gene: BBa_COO40 and BBa_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

ParisSaclay 09072015 - Quantification.jpg

Quantification

by Pauline and Audrey

Preparation of Agarose Gel 1%, 0,5g in 50mL of 1X TAE, 0,5µL of BET Migration 0,06A 80V We quantify with the electrophoresis gel:

  • BBa_C0040: 10ng/µL
  • BBa_J23101: 20ng/µL
  • BBa_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

Back to the calendar