Template:Team:KULeuven/20 August 2009/VanillinProduction

From 2009.igem.org

(Difference between revisions)
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* We performed a digest with EcoRI and SpeI to cut out the insert and check it's length. Enzymes were added separately, with 1h in between. Total volume was 30µl.
* We performed a digest with EcoRI and SpeI to cut out the insert and check it's length. Enzymes were added separately, with 1h in between. Total volume was 30µl.
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* {| border ="1" align="center"
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* Calculations restriction
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{| border ="1" align="center"
!| Part || µl DNA || µl MQ ||
!| Part || µl DNA || µl MQ ||
|- align="center"
|- align="center"
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* [[Test 2]]: cutting with 2 enzymes subsequently (1h incubation in between) in a volume of 30µl. Using a larger volume should dilute the glycerol, which inhibits cutting. After that, the products are incubated overnight to allow full restriction. Sam8 and Fcs are cut with EcoRI and SpeI; Sam5 and Ech are cut with EcoRI and XbaI
* [[Test 2]]: cutting with 2 enzymes subsequently (1h incubation in between) in a volume of 30µl. Using a larger volume should dilute the glycerol, which inhibits cutting. After that, the products are incubated overnight to allow full restriction. Sam8 and Fcs are cut with EcoRI and SpeI; Sam5 and Ech are cut with EcoRI and XbaI
-
*{| border ="1" align="center"
+
* Calculations restriction
 +
{| border ="1" align="center"
!| Part || µl DNA || µl MQ ||
!| Part || µl DNA || µl MQ ||
|- align="center"
|- align="center"

Revision as of 11:56, 20 August 2009

1)

  • EF colonies present! So, we miniprepped them in triple
  • Nanodrop concentrations:
Part concentration (ng/μl) 260/280 λ
EF A 74,9 1,89
EF B 63,1 1,87
EF C 53,9 1,90
  • We performed a digest with EcoRI and SpeI to cut out the insert and check it's length. Enzymes were added separately, with 1h in between. Total volume was 30µl.
  • Calculations restriction
Part µl DNA µl MQ
EF C 9,3 20,7


2)

  • Test 1: Results from yesterday's restriction test were inconclusive, because the DNA ladder didn't run properly so the length of the fragments couldn't be read. Therefore, we did it again...
  • Restriction=OK! Test 1 completed.


3)

  • Test 2: cutting with 2 enzymes subsequently (1h incubation in between) in a volume of 30µl. Using a larger volume should dilute the glycerol, which inhibits cutting. After that, the products are incubated overnight to allow full restriction. Sam8 and Fcs are cut with EcoRI and SpeI; Sam5 and Ech are cut with EcoRI and XbaI
  • Calculations restriction
Part µl DNA µl MQ
Sam8 B 7,9 22,1
Sam5 B 4,0 26,0
Ech B 5,2 24,8
Fcs B 4,4 25,6