Team:Paris Saclay/Notebook/June/21

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(Lab work)
 
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=='''Lab work'''==
=='''Lab work'''==
-
- Oligonucleotides determined for the BioBrick to FNR  
+
- Determined oligonucleotides for the BioBrick to FNR  
-
- Research on the binding sites of bphR 1, and research the possible induction of bphR2 to PCB
+
- Research on the binding sites of bphR1, and research the possible induction of bphR2 to PCB
-
- Design BioBricks with genes Pseudomonas pseudoalcaligenes KF707 and rhodococcus rhodochrous, it was done but the sequences only derived from one of the strains, namely, burkholderia xenovorans LB400
+
- Design BioBricks with genes ''Pseudomonas pseudoalcaligenes'' KF707 and ''Rhodococcus rhodochrous'', it was done but the sequences only derived from one of the strains, namely, ''Burkholderia xenovorans'' LB400
-
- Choice of the reporter system, beta-galactosidase or chromosome
+
- Choice of the reporter system, beta-galactosidase or chromoprotein.

Latest revision as of 00:16, 5 October 2013

Notebook : June 21

Lab work

- Determined oligonucleotides for the BioBrick to FNR

- Research on the binding sites of bphR1, and research the possible induction of bphR2 to PCB

- Design BioBricks with genes Pseudomonas pseudoalcaligenes KF707 and Rhodococcus rhodochrous, it was done but the sequences only derived from one of the strains, namely, Burkholderia xenovorans LB400

- Choice of the reporter system, beta-galactosidase or chromoprotein.


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