Team:Paris/September 8

From 2008.igem.org

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(Digestion)
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*We purifed our digestion products by gel extraction (Qiagen kit)
*We purifed our digestion products by gel extraction (Qiagen kit)
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*After elution, we obtained [DNA] = 25 ng/µL (based on the intensity of the band)
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*After elution, we obtained [DNA] ~ 25 ng/µL (based on the intensity of the band)
== Overnight ligation (16°C)==
== Overnight ligation (16°C)==

Revision as of 14:30, 12 September 2008

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Contents

Checking our ligases

Since our ligation experiments didn't work during these few days, we presume that our problem came from the ligases. That's why we decided to check the activity of the ligases in our possession. To do so:

  • we will digest a plasmid with only one restriction enzyme (EcoRI).
  • then we will try to ligate it back using our ligases.

Condition tested

Before gel excision
well n°4: undigested plasmid (MP101.1)
well °6, 7, 8, 9: digested plasmid (D202)
After gel excision
After purification
ligase incubation time amount of enzyme
L1 (ligase 1) 2h00 2 U (unit)
L1 2h00 400 U
L1 O/N 2 U
L1 O/N 400 U
L2 (ligase 2) 2h00 2 U
L2 2h00 400 U
L2 O/N 2 U
L2 O/N 400 U

Digestion

Reaction mixture (carried out four times )

  • ADN (MP101.1): 3.8 µL
  • H2O: 21.9 µL
  • 10X Buffer: 3 µL
  • BSA: 0.3 µl
  • EcoRI: 1 µL

Purification

  • We purifed our digestion products by gel extraction (Qiagen kit)
  • After elution, we obtained [DNA] ~ 25 ng/µL (based on the intensity of the band)

Overnight ligation (16°C)

  • DNA: 4 µL
  • 10X Buffer: 2 µL
  • Ligase: 1 µL
  • H2O: 13 µL