Exeter/24 July 2013

Results of liquid cultures

Some of our liquid cultures didn't work; the cells died in the antibiotic. Mildly frustrating. The failed cultures were:

• OmpR (BBa_K098011)
• Lambda inverter system (BBa_Q04510)

Minipreps using the Qiagen kit

We miniprepped:

• CcaR

• Promoter, RBS x 3 replicates

• CcaS

• B0034

• Magenta

• OmpR promoter

• OmpR

• YF1

• Lambda inverta

• Fix J

• Yellow

• Fix J promoter

Glycerol stocks

We made glycerol stocks of what is above, then stored them at -80^oC

For future reference, to get glycerol stocks back as plates, take a loop and streak on gel. Has to be taken from frozen glycerol stocks, which are immediately returned to the freezer.

We then made a gel for digests using ethidium bromide.

NanoDrop from miniprep

No SureClean was needed.

Digestion

We then cut the genes out of the plasmid using Xbal and Pstl. Prepare to run on a gel.

Each eppendorf contains:

• 12ul purite water

• 2ul 10X FastDigest Buffer w.Green

• 0.5ul Xbal

• 0.5ul Pstl

• 5ul DNA

In gel

The gel shows that some of our digestions appear to have worked (our yellow pigment in lane 6 has a clear band at about ~700bp, where would expect) but others appear not to have worked, or have bands that don't match our expected genes.

Cph8 gel

We're still uncertain about the presence of a PstI cut site in BBa_K322124 (cph8, our red light sensor), so we want to try cutting it with different combination of EcoRI, XbaI, SpeI and PstI. We have five replicates of cph8 plasmid from previous MiniPreps.

• cph8 #3

• cph8 #4

• cph8 #5

• cph8 #6

• cph8 #7

Unfortunately, they were only cut with Xbal and Pstl (Fran...), but this gel can be correctly run tomorrow with relative ease.

The lanes were run in the order above, flanked by a 1kb Gene Ruler.

Take me back to the notebook.