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Team:Tokyo Metropolitan/Notebook/Fiber/2010/09/15
From 2010.igem.org
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{{:Team:Tokyo_Metropolitan/Notebook/Fiber}} | {{:Team:Tokyo_Metropolitan/Notebook/Fiber}} | ||
| - | + | __NOTOC__ | |
==2010/9/15 Wednesday (Naoto)== | ==2010/9/15 Wednesday (Naoto)== | ||
===Experiment:Electrophoresis=== | ===Experiment:Electrophoresis=== | ||
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*PCR production (pSB1C3) | *PCR production (pSB1C3) | ||
| - | If you want to know other materials, see protocol4 | + | If you want to know other materials, see <html><a href="https://2010.igem.org/Team:Tokyo_Metropolitan/Project/Fiber/Protocol#.E3.80.80">the protocol4</a></html> |
| + | |||
'''procedure''' | '''procedure''' | ||
| - | see protocol4 | + | see <html><a href="https://2010.igem.org/Team:Tokyo_Metropolitan/Project/Fiber/Protocol#.E3.80.80Direct_PCR">the protocol4</a></html> |
| + | |||
'''result''' | '''result''' | ||
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see protocol1 | see protocol1 | ||
| - | A.xylinum( | + | A.xylinum(sub-cultured at 8/24 and 9/1) |
'''procedure''' | '''procedure''' | ||
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*pSB1C3 in agarose gel | *pSB1C3 in agarose gel | ||
| - | If you want to know other materials, see | + | If you want to know other materials, see <html><a href="https://2010.igem.org/Team:Tokyo_Metropolitan/Project/Fiber/Protocol#.E3.80.80">the protocol5</a></html> |
| + | |||
'''procedure''' | '''procedure''' | ||
| - | see protocol5 | + | see <html><a href="https://2010.igem.org/Team:Tokyo_Metropolitan/Project/Fiber/Protocol#.E3.80.80Direct_PCR">the protocol5</a></html> |
| + | |||
===Experiment:PCR=== | ===Experiment:PCR=== | ||
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*pSB1C3,bcsB(''A.xylinum'') | *pSB1C3,bcsB(''A.xylinum'') | ||
*a culture of ''E.coli'' | *a culture of ''E.coli'' | ||
| - | If you want to know other materials, see protocol3 | + | If you want to know other materials, see <html><a href="https://2010.igem.org/Team:Tokyo_Metropolitan/Project/Fiber/Protocol#.E3.80.80PCR">the protocol3</a></html> |
'''procedure''' | '''procedure''' | ||
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*PCR production (see above PCR) | *PCR production (see above PCR) | ||
| - | If you want to know other materials, see protocol4 | + | If you want to know other materials, see <html><a href="https://2010.igem.org/Team:Tokyo_Metropolitan/Project/Fiber/Protocol#.E3.80.80Direct_PCR">the protocol4</a></html> |
'''procedure''' | '''procedure''' | ||
| - | see protocol4 | + | see <html><a href="https://2010.igem.org/Team:Tokyo_Metropolitan/Project/Fiber/Protocol#.E3.80.80Direct_PCR">the protocol4</a></html> |
'''result''' | '''result''' | ||
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'''procedure''' | '''procedure''' | ||
| - | + | see <html><a href="https://2010.igem.org/Team:Tokyo_Metropolitan/Project/Fiber/Protocol#.E3.80.80Direct_PCR">the protocol5</a></html> | |
| + | |||
| + | |||
| + | |||
| + | |||
| + | <br/> | ||
Latest revision as of 17:40, 24 October 2010
E.coli Fiber Project Notebook
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2010/9/15 Wednesday (Naoto)
Experiment:Electrophoresis
member
naoto and watachin
material
- PCR production (pSB1C3)
If you want to know other materials, see the protocol4
procedure
see the protocol4
result
bands could be seen slightly
Experiment:subculture of A.xylinum
member
naoto and watachin
material
see protocol1 A.xylinum(sub-cultured at 8/24 and 9/1)
procedure
see protocol1 we made 3 OWW plates and 3 tubes of broth
Experiment:Extraction of DNA from agarose gel with QIAGEN
member
naoto and watachin
material
- pSB1C3 in agarose gel
If you want to know other materials, see the protocol5
procedure
see the protocol5
Experiment:PCR
member
naoto and watachin
material
- pSB1C3,bcsB(A.xylinum)
- a culture of E.coli
If you want to know other materials, see the protocol3
procedure
- add materials to PCR tubes
- PCR reaction (see below)
- nitialization :95°C 3min
- denaturation:96°C 1min
- annealing :51°C 1min
- elongation:72°C 3min
(30cycles from 96°C 1min to 72°C 3min)
- reaction stop :10°C ∞
Experiment:Electrophoresis
member
naoto and watachin
material
- PCR production (see above PCR)
If you want to know other materials, see the protocol4
procedure
see the protocol4
result
a band of pSB1C3 could be seen slightly bands of bcsB(A.xylinum),bcsC(E.coli) appeared clearly
Experiment:Digestion
member naoto and watachin
material
- pSB1C3,bcsA(A.xylinum) and bcsC(E.coli)
- 10×Mbuffer
- BSA
- XbaI
- SpeI
| pBS1C3 | bcsA | bcsC | ||
|---|---|---|---|---|
| solution of bcs(μl) | 50 | 50 | 50 | |
| 10×Mbuffer(μl) | 5 | 5 | 5 | |
| BSA(μl) | 5 | 5 | 5 | |
| XbaI(μl) | 1 | 1 | 1 | |
| SpeI(ul) | 1 | 1 | 1 |
procedure
- add "material" to PCR tubes(show below)
- incubation at 37℃,14h
Experiment:Extraction of DNA from agarose gel
member
naoto and watachin
material
- pSB1C3,bcsB(A.xylinum) and bcsC(E.coli) in agarose gel
If you want to know other materials, see the protocol5
procedure
see the protocol5
