My Notes II
From 2008.igem.org
07 August 2008 (Th)
- Picked colonies for sca2-7; streaked on CK plate, screened on Amp. Growing overnight in CK media
- mini meeting - new methods enforced due to assembly status:
Assembly Status:
All transfers completed successfully, EXCEPT sca2 (rbs1-A) and sca3 (fimH) Layer one assemblies completed: sca21-{<phoA!}.{b1006} sca22-{<AP!}.{b1006} sca23-{<HA!}.{b1006} sca24-{<myc!}.{b1006} sca25-{<FLAG!}.{b1006} None of Layer 2 or 3.
- Decided to shrink old tree and use new methods to finish the tags: attach my {<tag!}.{b1006} parts to {FimH}.{phoA!}
- Take existing {FimH}.{PhoA!} (aka. pBca1102-Bca9194), set up PCR using ca998 oligo and mea37 (<phoA> reverse oligo) to remove stop codon
- At first, the PCR product came out mysteriously large. We tried 3 times and the same thing occurred.
It was not until 11:00pm, that figured that I was using the wrong oligo ... we set up the 4th PCR then - with the correct oligo.
- also amplified Bca9194 for personal stock, since we were running low - grew on amp plate AND amp media