Exeter/9 July 2013

From 2013.igem.org

(Difference between revisions)
(Created page with "'''Our requested DNA has arrived from iGEM!''' The Parts sent over were... - Magenta pigment coding (BBa_K592012, pSB1C3) - Green light sensor (BBa_K592001, pSB1C3) - Yellow ...")
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- 2 Genome Integration Kits (BBa_K510000 and BBa_K510012). We know we want to genome integrate some of our Parts at some point...
- 2 Genome Integration Kits (BBa_K510000 and BBa_K510012). We know we want to genome integrate some of our Parts at some point...
-
- Alternative
+
- Alternative cyan pigments (BBa_K592011 just codes for the pigment but has no promoter, RBS or terminator. BBa_K864404 codes for the same pigment, but has a promoter and RBS. BBa_K592022 also has the same coding region and RBS, but an alternative promoter)
 +
 
 +
 
 +
== Afternoon ==
 +
 
 +
'''Transforming the BioBricks we will be utilising in the blue light module'''
 +
 
 +
We are transforming...
 +
 
 +
- BBa_K608002, codes for a promoter and RBS
 +
 
 +
- BBa_K592004, our blue light sensor
 +
 
 +
- BBa_B0010, a terminator
 +
 
 +
- BBa_B0015, a terminator
 +
 
 +
- BBa_B0034, an RBS
 +
 
 +
- K592006, the promoter that is activated by FixJ
 +
 
 +
We already have the following Parts as LB stab plates from the iGEM registry, so transformation of these Parts is required:
 +
 
 +
- BBa_K592005, codes for our intermediate protein, FixJ
 +
 
 +
- BBa_K592010, our yellow pigment
 +
 
 +
The transformation protocol from 4/7/13 was followed, no details from the method were changed.
 +
 
 +
'''Sequencing'''
 +
 
 +
We also sent our cph8 plasmids off for sequencing.
 +
 
 +
'''Liquid cultures'''
 +
 
 +
Liquid cultures were made of...
 +
 
 +
- BBa_K592012, our magenta pigment
 +
 
 +
- BBa_K592010, our yellow pigment
 +
 
 +
- BBa_K322122, our magenta pigment

Revision as of 10:24, 16 July 2013

Our requested DNA has arrived from iGEM!

The Parts sent over were...

- Magenta pigment coding (BBa_K592012, pSB1C3)

- Green light sensor (BBa_K592001, pSB1C3)

- Yellow pigment coding (BBa_K592010, pSB1C3)

- Cyan pigment coding (BBa_K322122, pSB1C3)

- FixJ intermediate protein coding (BBa_K592005, pSB1C3)

We also requested some extra parts from the Registry

- 2 Genome Integration Kits (BBa_K510000 and BBa_K510012). We know we want to genome integrate some of our Parts at some point...

- Alternative cyan pigments (BBa_K592011 just codes for the pigment but has no promoter, RBS or terminator. BBa_K864404 codes for the same pigment, but has a promoter and RBS. BBa_K592022 also has the same coding region and RBS, but an alternative promoter)


Afternoon

Transforming the BioBricks we will be utilising in the blue light module

We are transforming...

- BBa_K608002, codes for a promoter and RBS

- BBa_K592004, our blue light sensor

- BBa_B0010, a terminator

- BBa_B0015, a terminator

- BBa_B0034, an RBS

- K592006, the promoter that is activated by FixJ

We already have the following Parts as LB stab plates from the iGEM registry, so transformation of these Parts is required:

- BBa_K592005, codes for our intermediate protein, FixJ

- BBa_K592010, our yellow pigment

The transformation protocol from 4/7/13 was followed, no details from the method were changed.

Sequencing

We also sent our cph8 plasmids off for sequencing.

Liquid cultures

Liquid cultures were made of...

- BBa_K592012, our magenta pigment

- BBa_K592010, our yellow pigment

- BBa_K322122, our magenta pigment