Team:Paris Saclay/Notebook/August/25

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Contents

Monday 25th August

Lab work

B - Construction of the fusion protein

plasmid extraction : pGEMTeasy + chromoprotein

by Laetitia

We used the bacteria containing pGEMTeasy + chromoprotein launched by Melanie sunday the 24th for the plasmid extraction, 6 independent cultures which come from 6 independent colonies.

We made a stock of bacteria for each sample (x6).

To extract the plasmid, we used the plasmid DNA purification kit (Macherey-Nagel).

Digestion of pGEMTeasy+chromoproteinby XbaI and PstI

by Laetitia

The goal is to check the presence of the insert inside the plasmid. We digest the 6 samples of purified plasmid.

component volume
Plasmid 5 μl
Fast Digest buffer 10X 1μl
XbaI 0.5μl
PstI 0.5μl
H20 3μl

1h at 37°C

Electrophoresis of the digestion product of pGEMTeasy+chromoprotein

by Laetitia

T : control negatif without enzyme

D : sample digested by XbaI and PstI

T1 - D1 - T2 - D2 - T3 - D3 - E - T4 - D4 - T5 - o - D6

250814 laetitia digestion verif chromoP pGEMTeasy.jpg

Results : lost of the sample D5 in a hole in the agarose gel

The samples 3, 4 and 6 seems to contain the chromoprotein gene (two bands)

--> We will try another plasmid extraction because the electrophoresis profil doesn't show bands for every sample.

Bacterial culture of DH5a containing pGEMTeasy + chromprotein

by Laetitia

We launched 6 cultures in 5mL LB + Ampi (1/1000) - 37°C at night . The bacteria come from the stock made before the plasmid extraction

D - Lemon Scent

Gel electrophoresis of CAD

by Sean

Veirfication of the purification from Friday

Legend

  1. ladder 10µl
  2. PCR result of CAD

Paris Saclay Sean 140825.jpg

CAD ligation in pPS1

by Mélanie pPSI was previously digest by PacI and dephosphorylated We want to insert the CAD PCR fragment in pPSI to make pPS5.

component volume
PCR CAD 10 μl
pPS1 3μl
10x buffer ligase 2μl
ligase 1μl
H20 4μl

4H at room temperature

Transformation of DH5a with the ligation =

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