Team:DTU-Denmark/Notebook/6 September 2013

From 2013.igem.org

(Difference between revisions)
(Who was in the lab)
 
Line 80: Line 80:
[[File:2013-09-06 HAO USER td.jpg|600px]]
[[File:2013-09-06 HAO USER td.jpg|600px]]
-
==Conclusion==
 
-
<hr/>
 

Latest revision as of 10:55, 4 October 2013

6 September 2013

Navigate to the Previous or the Next Entry

Contents

Lab 208


Main purpose


  • Add USER endings to HAO gene extracted from Nitrosomonas europaea

Who was in the lab


Henrike

Procedure


Repeat HAO USER PCR from yesterday with same conditions and programs

Template: HAO extraction fragment -isolated from Nitrosomonas europea- (purified from PCR run on 04.09)

Primers: 18a & 18b

Two versions, one with 5% DMSO and one with 3% DMSO and two programs: Touchdown (62C -> 55) and a single annealing temperature of 59C.

PCR reaction master mix

compound volume (uL)
dNTPs 1
HF 10
polymerase x7 0.5
FW 3
RV 3
template 1
MQ 29
DMSO 1.5
  • Add 49 ul of the master mix, and
  • Add 1 ul DMSO (for the 5%) or 1 ul of MQ (for the 3%)

User reaction

was performed with HAO User fragment that was purified yesterday (but had low concentration) and pZA21::ara (promoter from the Biobrick K808000) and pZA21 with a tight arabinose promoter (from our SPL). Also Nir 1 User and Nir 2 User were ligated into the pZA21 ara tight for Nir. Negative controls were made for all three backbones.

Results


Gel 1

Gel of yesterday's PCR was empty (we lost the picture though...)

PCR was redone.

Gel 2

For the PCR results of today.

  • 2-log ladder
  • HAO User on 59C, 3% DMSO
  • HAO User on 59C, 5% DMSO
  • 2-log ladder

2013-09-06 HAO USER 59.jpg

Gel 3

  • 2-log ladder
  • HAO User on touchdown, 3% DMSO
  • HAO User on touchdown, 5% DMSO
  • 2-log ladder

2013-09-06 HAO USER td.jpg


Navigate to the Previous or the Next Entry