Team:DTU-Denmark/Notebook/13 August 2013
From 2013.igem.org
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Used 5% DMSO, 2 uL of mM MgCl2 and GC-buffer. | Used 5% DMSO, 2 uL of mM MgCl2 and GC-buffer. | ||
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+ | constitutive SPL | ||
+ | *template: pZA21::RFP | ||
+ | *primers: 52a, 52b1 | ||
+ | |||
+ | constitutive reference | ||
+ | *template: pZA21::RFP | ||
+ | *primers: 52a, 52b2 | ||
+ | |||
+ | arabinose reference | ||
+ | *template: | ||
+ | *primers: 51a,51b1 | ||
+ | |||
+ | program | ||
==Results== | ==Results== |
Revision as of 12:17, 13 August 2013
13 August 2013
Contents |
lab 208
Main purpose
Who was in the lab
Kristian, Henrike, Gosia
Procedure
PCR (promoter library)
PCR to amplify USER fragments of the constitutive SPL, the constitutive reference promoter and the arabinose reference promoter.
Used 5% DMSO, 2 uL of mM MgCl2 and GC-buffer.
constitutive SPL
- template: pZA21::RFP
- primers: 52a, 52b1
constitutive reference
- template: pZA21::RFP
- primers: 52a, 52b2
arabinose reference
- template:
- primers: 51a,51b1
program
Results
Each gel is representing one row; from left to right and up to down is row A to H:
Conclusion
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