Team:Chiba/Calendar-Home/21 August 2008

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20 August 2008 <|> 22 August 2008

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Laboratory work

Team:Input

(-->20/8)

Inoculated transformants for 12 hours in LB 2mL containing Ampicillin.

BBa_J22141:After inoculated for 11 hours, added 20μl IPTG and cultured one hour.


  • UV irradiation test (plate phase)
  • two plasmids from(JW1908)
    • (Repressor)-Ptrc-LuxR-Plux-cI-colE1-Amp-
    • (Reporter)-PcI-GFP-p15a-Cm-
  1. Inoculated (Reporter) culture from glycerol stock(-80°C freezer) in 2mL LB medium.(LB-Amp,Cm)(LB-Amp,Cm,AHL100nM)


Inoculated transformants for 12 hours in 2ml LB-Ampicillin, Chloramphenicol medium and LB-Ampicillin, Chloramphenicol, 100nmAHL medium .(37&ged;C, 12h). Diluted 10^5-fold, and plated 20ul of the resulting solution to (LB-Amp,Cm)(LB-Amp,cm,AHL100nM) plates each other and cultured for 12h at 37°C.
37°Cで12h培養後、きちんとコロニーができていることを確認し、両方のプレートにUVを照射する。UVの波長は254nm,UVランプとプレートの距離は14cm。
UVを照射して9h後、21h後にそれぞれ両方のプレートに次の同じ操作をする。
両方のプレートのコロニーをつついてそれぞれ(LB-Amp,Cm),(LB-Amp,Cm,AHL100nM)2ml培養する。
37°C,で12h培養後、濁っていたので、それぞれを(LB-Amp,Cm),(LB-Amp,Cm,AHL100nM)のプレートに105希釈して20μl撒いた。


  • Colony count
no AHLAHL100nM
9h 606453
12h 146151

Colonies of no AHL plate were AHLが入っていないほうのコロニーはいづれも光っていた。→機能チェックはOK

Team:Communication

(20/8)--->PCR


DNA Template 1
dNTP mix 10
Foward Primer 5
Reverse Primer 5
DNA polymerase TAQ 1
Thermopol Buffer 5
dH2O 28
TOTAL 50μL


95°C,5min -> ( 95°C,1min -> 52°C,1min -> 72°C,1min )・・・25cycles -> 72°C,10min -> 6°C


--->Gel Check
Chiba-0821.JPG
Sample DNA 3
Loading Dye 2
dH2O 7
TOTAL 12μL
From left;


Transformation
competent cells : XL10G



--->(23/8)Digestion

Team:Output

Transformation