Team:Tokyo Metropolitan/Notebook/Fiber/2010/10/24
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__NOTOC__ | __NOTOC__ | ||
==2010/10/24 Sunday (Naoto)== | ==2010/10/24 Sunday (Naoto)== | ||
- | '''member''' | + | :'''member''' |
- | naoto and watachin | + | :naoto and watachin |
===Preparation:making preculture for Miniprep === | ===Preparation:making preculture for Miniprep === | ||
- | '''material''' | + | :'''material''' |
- | *colony of ''E.coli'' | + | :*colony of ''E.coli'' |
- | **bcsA→No.21,22 | + | :**bcsA→No.21,22 |
- | **bcsB→No.10 | + | :**bcsB→No.10 |
- | **bcsC→No.54,64 | + | :**bcsC→No.54,64 |
- | **bcsD→No.75 | + | :**bcsD→No.75 |
- | *LB+Cam broth | + | :*LB+Cam broth |
- | '''procedure''' | + | :'''procedure''' |
- | see <html><a href="https://2010.igem.org/Team:Tokyo_Metropolitan/Project/Fiber/Protocol#.E3.80.80Grow up culture of E.coli">protocol2</a></html> | + | :see <html><a href="https://2010.igem.org/Team:Tokyo_Metropolitan/Project/Fiber/Protocol#.E3.80.80Grow up culture of E.coli">protocol2</a></html> |
===Experiment:Ligation=== | ===Experiment:Ligation=== | ||
- | '''material''' | + | :'''material''' |
- | see <html><a href="https://2010.igem.org/Team:Tokyo_Metropolitan/Project/Fiber/Protocol#.E3.80.80ligation">protocol8</a></html> | + | :see <html><a href="https://2010.igem.org/Team:Tokyo_Metropolitan/Project/Fiber/Protocol#.E3.80.80ligation">protocol8</a></html> |
- | *vector | + | :*vector |
- | **pUC19(digested by XbaI) | + | :**pUC19(digested by XbaI) |
- | *Insert | + | :*Insert |
- | **bcsA(digested by XbaI+SpeI) | + | :**bcsA(digested by XbaI+SpeI) |
- | **bcsB(digested by XbaI+SpeI) | + | :**bcsB(digested by XbaI+SpeI) |
- | **bcsC(digested by XbaI+SpeI) | + | :**bcsC(digested by XbaI+SpeI) |
- | **bcsD(digested by XbaI+SpeI) | + | :**bcsD(digested by XbaI+SpeI) |
- | '''procedure''' | + | :'''procedure''' |
- | refer to <html><a href="https://2010.igem.org/Team:Tokyo_Metropolitan/Project/Fiber/Protocol#.E3.80.80ligation">protocol8</a></html> | + | :refer to <html><a href="https://2010.igem.org/Team:Tokyo_Metropolitan/Project/Fiber/Protocol#.E3.80.80ligation">protocol8</a></html> |
===Experiment:Transformation=== | ===Experiment:Transformation=== | ||
- | '''material''' | + | :'''material''' |
- | see <html><a href="https://2010.igem.org/Team:Tokyo_Metropolitan/Project/Fiber/Protocol#.E3.80.80transformation">protocol9</a></html> | + | :see <html><a href="https://2010.igem.org/Team:Tokyo_Metropolitan/Project/Fiber/Protocol#.E3.80.80transformation">protocol9</a></html> |
- | *Ecos JM109/Nova Blue(Competent Cell) | + | :*Ecos JM109/Nova Blue(Competent Cell) |
- | '''procedure''' | + | :'''procedure''' |
- | refer to <html><a href="https://2010.igem.org/Team:Tokyo_Metropolitan/Project/Fiber/Protocol#.E3.80.80transformation">protocol9</a></html> | + | :refer to <html><a href="https://2010.igem.org/Team:Tokyo_Metropolitan/Project/Fiber/Protocol#.E3.80.80transformation">protocol9</a></html> |
===Experiment:Miniprep=== | ===Experiment:Miniprep=== | ||
- | '''material''' | + | :'''material''' |
- | see <html><a href="https://2010.igem.org/Team:Tokyo_Metropolitan/Project/Fiber/Protocol#.E3.80.80miniprep">protocol10</a></html> | + | :see <html><a href="https://2010.igem.org/Team:Tokyo_Metropolitan/Project/Fiber/Protocol#.E3.80.80miniprep">protocol10</a></html> |
- | *Preculture | + | :*Preculture |
- | No.21,22:bcsA | + | :No.21,22:bcsA |
- | No.10:bcsB | + | :No.10:bcsB |
- | No.54,64:bcsC | + | :No.54,64:bcsC |
- | No.75:bcsD | + | :No.75:bcsD |
- | '''procedure''' | + | :'''procedure''' |
- | refer to <html><a href="https://2010.igem.org/Team:Tokyo_Metropolitan/Project/Fiber/Protocol#.E3.80.80miniprep">protocol10</a></html> | + | :refer to <html><a href="https://2010.igem.org/Team:Tokyo_Metropolitan/Project/Fiber/Protocol#.E3.80.80miniprep">protocol10</a></html> |
===Experiment:Sequence=== | ===Experiment:Sequence=== | ||
- | '''material''' | + | :'''material''' |
- | *DNA(No.21,22,10,54,64,75:following before "Miniprep") | + | :*PCR |
- | *Big Dye | + | :**DNA(No.21,22,10,54,64,75:following before "Miniprep") |
- | *primer | + | :**Big Dye |
- | *DW | + | :**primer |
- | *Ethanol precipitation | + | :**DW |
- | *ethanol | + | :*Ethanol precipitation |
- | *EDTA | + | :**ethanol |
+ | :**EDTA | ||
- | '''procedure''' | + | :'''procedure''' |
- | #mix materials(DNA<50ng) | + | :#mix materials(DNA<50ng) |
- | #PCR | + | :#PCR |
- | #Add EDTA and Ethanol and put at room temperature (15min) | + | :#Add EDTA and Ethanol and put at room temperature (15min) |
- | #centrifuge (8000rpm,30min) | + | :#centrifuge (8000rpm,30min) |
- | #throw away supernatant | + | :#throw away supernatant |
- | #add ethanol again | + | :#add ethanol again |
- | #centrifuge (8000rpm,15min) | + | :#centrifuge (8000rpm,15min) |
- | #put at refrigerator | + | :#put at refrigerator |
- | #throw away supernatant | + | :#throw away supernatant |
- | #add Hi-Di solution | + | :#add Hi-Di solution |
- | #transfer these sample to plate for sequence | + | :#transfer these sample to plate for sequence |
- | #read sequence | + | :#read sequence |
<br/> | <br/> |
Latest revision as of 18:08, 27 October 2010
E.coli Fiber Project Notebook
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2010/10/24 Sunday (Naoto)
- member
- naoto and watachin
Preparation:making preculture for Miniprep
- material
- colony of E.coli
- bcsA→No.21,22
- bcsB→No.10
- bcsC→No.54,64
- bcsD→No.75
- LB+Cam broth
- colony of E.coli
- procedure
- see protocol2
Experiment:Ligation
- material
- see protocol8
- vector
- pUC19(digested by XbaI)
- Insert
- bcsA(digested by XbaI+SpeI)
- bcsB(digested by XbaI+SpeI)
- bcsC(digested by XbaI+SpeI)
- bcsD(digested by XbaI+SpeI)
- vector
- procedure
- refer to protocol8
Experiment:Transformation
- material
- see protocol9
- Ecos JM109/Nova Blue(Competent Cell)
- procedure
- refer to protocol9
Experiment:Miniprep
- material
- see protocol10
- Preculture
- No.21,22:bcsA
- No.10:bcsB
- No.54,64:bcsC
- No.75:bcsD
- procedure
- refer to protocol10
Experiment:Sequence
- material
- PCR
- DNA(No.21,22,10,54,64,75:following before "Miniprep")
- Big Dye
- primer
- DW
- Ethanol precipitation
- ethanol
- EDTA
- PCR
- 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