Formal Lab Session - 13th October 2009
- Today we decided not to characterize cotC+smtA biobricks since we won't have time to finish and we want to finish the lab work this week.
- We will do B.subtilis transformation using 3 strains cultured yesterday.
Experiment procedure
Preparation of parts to send to the registry
Measured the concentrations of the midipreps and prepared them to send to the parst registry
sspB:64 ng/ul
To parts registry: 6.4 ng/ul in 20ul
ara:34 ng/ul
To parts registry: 3.4 ng/ul in 20ul
ara+sspB:87.5 ng/ul
To parts registry: 8.75 ng/ul in 20ul
cotC+smtA:355.9 ng/ul
To parts registry: 9 ng/ul in 20ul
cwlJ:76.9 ng/ul
To parts registry: 7.69 ng/ul in 20ul
sleB:98.3 ng/ul
To parts registry: 5 ng/ul in 20ul
swlJ + sleB:55 ng/ul
To parts registry: 5.5 ng/ul in 20ul
Preparation of parts for sequencing
Prepared the primers for psB1AT3 (x2, prepared two sets)
Forward primer preparation: Total 30ul, 10pmol/ul
Forward primer : 10ul (30pmol/ul)
PCR water: 20ul
Reverse primer preparation: Total 30ul, 10pmol/ul
Forward primer : 7.5ul (40pmol/ul)
PCR water: 22.5ul
Placed into the box for sequencing parts
B.subtilis transformation
- Followed the standard protocol form our lab's B.subltilis 168 transformation protocal.
- Added 5ul pGFP-rrnB:kinA vector to all three strains.
- Plated the transformed cell on LB+Em+CHL plate
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