Team:Lethbridge CCS/Notebook
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=== 6 Sept 2008 === | === 6 Sept 2008 === | ||
- | + | (Peter, Paul, Marc, Glenda, Nathan) | |
- | - | + | |
+ | * looked at PCR results from 3 Sept; some extra bands (see picture) | ||
+ | ** [[Image:PCRTetR-GFP]] | ||
+ | * decided to do Agarose gel purification of pSB1A7 from 2 Sept and TetR-GFP from 3 Sept | ||
+ | * used pooled samples as follows: | ||
+ | ** pSB1A7: 1/100x at 62°C,1x and 1/10x at 66°C | ||
+ | ** TetR-GFP: all three 1x samples | ||
+ | * used Fermentas 1kb GeneRuler; ran at 1000 V for 25 minutes | ||
+ | * used MinElute Gel Extraction kit to purify | ||
+ | |||
+ | |||
- | |||
Revision as of 22:32, 6 September 2008
2 Sept 2008
(Peter, Paul, Elizabeth, Glenda, Nathan)
- Resuspended our primers (psB1A7 forward and reverse; TetR-GFP forward and reverse) to 100 μM.
- Made 10-fold dilutions of each primer
- Set up and ran PCR on psB1A7
- varied concentration of vector (1 x, 1/10 x, 1/100 x) and annealing temperatures (58°C, 62°C, 66°C), giving nine variations;
- used materials and amounts as per Phusion polymerase kit
- Cycling temperatures and times for PCR Initial denaturation 98°C 30 sec ___ Denaturation 98°C 10 sec | Annealing 58/62/66 °C 30 sec |--- 30 cycles Extension 72°C 1 min ___| Final extension 72°C 10 min Hold 4°C hold
3 Sept 2008
(Peter, Paul, Elizabeth, Marc, Glenda, Nathan)
- PCR of pSB1A7 from yesterday worked well; approximate size was expected to be ~2500 bp, which was verified (see below)
- did PCR with TetR-GFP using same 9 samples and cycling times/temperatures as yesterday except temperature gradient was 57°C-61°C-65°
6 Sept 2008
(Peter, Paul, Marc, Glenda, Nathan)
- looked at PCR results from 3 Sept; some extra bands (see picture)
- decided to do Agarose gel purification of pSB1A7 from 2 Sept and TetR-GFP from 3 Sept
- used pooled samples as follows:
- pSB1A7: 1/100x at 62°C,1x and 1/10x at 66°C
- TetR-GFP: all three 1x samples
- used Fermentas 1kb GeneRuler; ran at 1000 V for 25 minutes
- used MinElute Gel Extraction kit to purify