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CAROL
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WIKI CODING HERE
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CHINMOYEE
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EMILY
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- Performed a Colony PCR on LuxOD47E in psB1AC3 vector colonies from last week. Only digests done with XbaI / PstI enzymes produced colonies on plates, so these were the only colonies used.
- Used p Taq and LuxO forward and reverse primers. Cycling conditions were as follows: 94 C for 6 minutes, 36x (94 C for 30 sec, 55 C for 45 sec, 72 C for 90 sec), 72 C for 10 minutes and hold at 4 C.
- See gel photo below. Lanes 1-6 are LuxOD47E cut with XbaI / PstI, colonies 1-6, Lane 7 is a ngeative control with ddH2O.
- Results: Nothing was amplified. This was because I used the wrong buffer. Will proceed by re-running the Colony PCR with the CORRECT buffer (10x PCR Buffer- Cl2).
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FAHD
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IMAN
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JAMIE
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JEREMY
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KATIE
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KEVIN
Restreak
Restreak of R0040, B0015, and J13002 were done to grow more of verified single colonies.
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MANDY
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PATRICK
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PRIMA
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STEFAN
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VICKI
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