Team:Tokyo Metropolitan/Notebook/Fiber/2010/10/23
From 2010.igem.org
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naoto and watachin | naoto and watachin | ||
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+ | ===Experiment:Sequence=== | ||
+ | '''material''' | ||
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+ | For PCR | ||
+ | *bcsA (No.9) | ||
+ | *Big Dye | ||
+ | *primer | ||
+ | *DW | ||
+ | For Ethanol precipitation | ||
+ | *ethanol | ||
+ | *EDTA | ||
+ | |||
+ | '''procedure''' | ||
+ | #mix materials(DNA<50ng) | ||
+ | #PCR | ||
+ | #Add EDTA and Ethanol and put at room temperature (15min) | ||
+ | #centrifuge (8000rpm,30min) | ||
+ | #throw away supernatant | ||
+ | #add ethanol again | ||
+ | #centrifuge (8000rpm,15min) | ||
+ | #put at refrigerator | ||
+ | #throw away supernatant | ||
+ | #add Hi-Di solution | ||
+ | #transfer these sample to plate for sequence | ||
+ | #read sequence | ||
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+ | |||
+ | |||
+ | <br/> | ||
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===Experiment:Colony PCR=== | ===Experiment:Colony PCR=== | ||
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seem to be correct inserts | seem to be correct inserts | ||
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Revision as of 16:39, 25 October 2010
E.coli Fiber Project Notebook
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2010/10/23 Saturday (Naoto)
member
naoto and watachin
Experiment:Sequence
material
For PCR
- bcsA (No.9)
- Big Dye
- primer
- DW
For Ethanol precipitation
- ethanol
- EDTA
procedure
- mix materials(DNA<50ng)
- PCR
- Add EDTA and Ethanol and put at room temperature (15min)
- centrifuge (8000rpm,30min)
- throw away supernatant
- add ethanol again
- centrifuge (8000rpm,15min)
- put at refrigerator
- throw away supernatant
- add Hi-Di solution
- transfer these sample to plate for sequence
- read sequence
Experiment:Colony PCR
material
- colony of E.coli
- bcsB:1~32
- bcsC:33~64
- bcsD:65~96
other materials were same as protocol3
procedure
see protocol3
result
From the length of bands
bcsC→No.54 and 64
bcsD→No.75
seem to be correct inserts