Formal Lab Session - 7th October 2009
CotC PCR
We wanted to start from scracth for CotC biobrick. We will also PCR it.
CotC
1ul of CotC biobrick synthesised in PMK
39ul of PCR water
GoTaq
2ul GoTaq
18ul H2O
PCR Mix:
per tube: 10ul 5xGoTaq buffer prepared above + 5uk DNTP
Tubes(Prepared 6 tubes):
26ul H2O
15ul PCR mx
2.5 ul forward primer (It was diluted before)
2.5 ul reverse primer
2ul template prepared above (For the 6. tube, control tube, used water instead)
We setup 6 PCR reactions in two groups.
Group 1 (3 tubes)
50C annealing temperature
90seconds extesnion time
31 cycles
Group 1 (2 tubes + control)
52C annealing temperature
90seconds extesnion time
31 cycles
we run the PCR products on the gel . run 8uk os PCR product from 6 tubes. The results were good for all tubes. We then cleaned the PCR products using the PCR clean-up kit.
Restriction Digest for pmutin4
We did restriction digest with two controls to see is the enzymes were working well. If they work we will clean the gel for pmutin4.
pmutin4 Digest with HindIII and BamHI
H20 26ul
10x Buffer E 5ul
DNA 15ul
HindIII 2ul
BamHI 2ul
pmutin4 Digest with HindIII only
H20 15.5ul
10x Buffer E 2ul
DNA 2ul
HindIII 0.5ul
pmutin4 Digest with BamHI only
H20 15.5ul
10x Buffer E 2ul
DNA 2ul
BamHIIII 0.5ul
Mixed the tubes well and incubated for three hours at 37C
In the meantime prepared 1xTAE buffer and 0.8% agarose gel.
Run the digests on the gel
Digest1:50ul from the digest + 10ul 10X loading buffer
Digest2:9ul from the digest + 1ul 10X loading buffer
Digest3:9ul from the digest + 1ul 10X loading buffer
pmutin 4 digest results were not very clear!
July
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