Team:Tokyo Metropolitan/Notebook/Fiber/2010/09/29
From 2010.igem.org
(New page: {{:Team:Tokyo_Metropolitan/Header}} ==2010/09/29 Wednesday (Naoto)== ===Experiment:Electrophoresis of insert check PCR=== '''member''' naoto and bambi75 '''material''' *PCR production ...) |
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==2010/09/29 Wednesday (Naoto)== | ==2010/09/29 Wednesday (Naoto)== | ||
- | ===Experiment: | + | ===Experiment:Insert check PCR=== |
'''member''' | '''member''' | ||
- | naoto and | + | naoto and NEX |
'''material''' | '''material''' | ||
- | * | + | *bcsC,D(''A.xylinum'') in colonies of '''E.coli''' |
- | If you want to know other materials,refer to | + | If you want to know other materials,refer to protocol3 |
'''procedure''' | '''procedure''' | ||
- | see | + | see protocol3 |
- | + | ||
- | + | ||
- | + | ||
- | ===Experiment: | + | ===Experiment:PCR of PT7-RBS-bcsA~D(''A.xylinum''),PT7-RBS-E~G(E.coli),bcsQ(''E.coli''),RBS-T7polymerase=== |
'''member''' | '''member''' | ||
- | naoto and | + | naoto and NEX |
'''material''' | '''material''' | ||
- | * | + | *A colony of ''A.xylinum'' |
- | If you want to know other materials,refer to | + | *bcsE~G(E.coli) |
+ | *bcsQ(''E.coli'') | ||
+ | *T7polymerase(BBa_K145001) | ||
+ | If you want to know other materials,refer to protocol3 | ||
'''procedure''' | '''procedure''' | ||
- | see | + | see protocol3 |
- | + | ===Experiment:digestion of bcsB(''E.coli'')=== | |
- | + | ||
- | + | ||
- | ===Experiment: | + | |
'''member''' | '''member''' | ||
- | naoto and | + | naoto and easily |
'''material''' | '''material''' | ||
- | * | + | *bcsB(''E.coli'') |
- | If you want to know other materials,refer to | + | If you want to know other materials,refer to protocol6 |
'''procedure''' | '''procedure''' | ||
- | + | follow to protocol6 | |
- | ===Experiment: | + | ===Experiment:subculture of ''A.xylinum''=== |
'''member''' | '''member''' | ||
- | naoto and | + | naoto and easily |
'''material''' | '''material''' | ||
- | + | see protocol1 | |
- | + | A.xylinum(subcultured at 9/1) | |
'''procedure''' | '''procedure''' | ||
- | + | see protocol1 | |
- | ===Experiment: | + | ===Experiment:Transformation=== |
'''member''' | '''member''' | ||
- | naoto and | + | naoto and easily |
'''material''' | '''material''' | ||
- | * | + | *parts of bcsA,B(''A.xylinum'') |
- | If you want to know other materials,refer to | + | If you want to know other materials,refer to protocol8 |
'''procedure''' | '''procedure''' | ||
- | + | see protocol8 | |
- | ===Experiment:Electrophoresis of | + | ===Experiment:Electrophoresis of insert check PCR=== |
'''member''' | '''member''' | ||
- | naoto | + | naoto |
'''material''' | '''material''' | ||
- | *PCR production ( | + | *PCR production (bcsC,D(''A.xylinum'') ) |
If you want to know other materials,refer to protocol4 | If you want to know other materials,refer to protocol4 | ||
Line 93: | Line 90: | ||
'''result''' | '''result''' | ||
- | |||
- | ===Experiment: | + | Bands(102 and 104) of bcsD(''A.xylinum'') could be seen slightly |
+ | |||
+ | So we prepared precultures for miniprep | ||
+ | |||
+ | ===Experiment:Electrophoresis of PT7-RBS-bcsA~D(''A.xylinum''),PT7-RBS-E~G(E.coli)=== | ||
'''member''' | '''member''' | ||
- | naoto | + | naoto |
'''material''' | '''material''' | ||
- | * | + | *PCR production (PT7-RBS-bcsA~D(''A.xylinum''),PT7-RBS-E~G(E.coli)) |
- | If you want to know other materials,refer to | + | If you want to know other materials,refer to protocol4 |
'''procedure''' | '''procedure''' | ||
- | see | + | see protocol4 |
+ | |||
+ | '''result''' | ||
+ | |||
+ | All bands differed from collect length |
Revision as of 15:36, 3 October 2010
2010/09/29 Wednesday (Naoto)
Experiment:Insert check PCR
member
naoto and NEX
material
- bcsC,D(A.xylinum) in colonies of E.coli
If you want to know other materials,refer to protocol3
procedure
see protocol3
Experiment:PCR of PT7-RBS-bcsA~D(A.xylinum),PT7-RBS-E~G(E.coli),bcsQ(E.coli),RBS-T7polymerase
member
naoto and NEX
material
- A colony of A.xylinum
- bcsE~G(E.coli)
- bcsQ(E.coli)
- T7polymerase(BBa_K145001)
If you want to know other materials,refer to protocol3
procedure
see protocol3
Experiment:digestion of bcsB(E.coli)
member
naoto and easily
material
- bcsB(E.coli)
If you want to know other materials,refer to protocol6
procedure
follow to protocol6
Experiment:subculture of A.xylinum
member
naoto and easily
material
see protocol1 A.xylinum(subcultured at 9/1)
procedure
see protocol1
Experiment:Transformation
member
naoto and easily
material
- parts of bcsA,B(A.xylinum)
If you want to know other materials,refer to protocol8
procedure
see protocol8
Experiment:Electrophoresis of insert check PCR
member
naoto
material
- PCR production (bcsC,D(A.xylinum) )
If you want to know other materials,refer to protocol4
procedure
see protocol4
result
Bands(102 and 104) of bcsD(A.xylinum) could be seen slightly
So we prepared precultures for miniprep
Experiment:Electrophoresis of PT7-RBS-bcsA~D(A.xylinum),PT7-RBS-E~G(E.coli)
member
naoto
material
- PCR production (PT7-RBS-bcsA~D(A.xylinum),PT7-RBS-E~G(E.coli))
If you want to know other materials,refer to protocol4
procedure
see protocol4
result
All bands differed from collect length