Team:Chiba/Calendar-Home/21 August 2008

From 2008.igem.org

(Difference between revisions)
(Team:Input)
(Team:Communication)
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===Team:Communication===
===Team:Communication===
:(20/8)--->'''[[Team:Chiba/protocol/PCR|PCR]]'''
:(20/8)--->'''[[Team:Chiba/protocol/PCR|PCR]]'''
-
::*BBa_C0070(2007) [http://partsregistry.org/Part:BBa_C0070]
+
::*[http://partsregistry.org/Part:BBa_C0070 BBa_C0070](2007)
-
::*BBa_C0070(2006) [http://partsregistry.org/Part:BBa_C0070]
+
::*[http://partsregistry.org/Part:BBa_C0070 BBa_C0070](2006)
-
::*BBa_C0076(2007) [http://partsregistry.org/Part:BBa_C0076]
+
::*[http://partsregistry.org/Part:BBa_C0076 BBa_C0076](2007)
-
::*BBa_C0078(2007) [http://partsregistry.org/Part:BBa_C0078]
+
::*[http://partsregistry.org/Part:BBa_C0078 BBa_C0078](2007)
-
::*BBa_C0078(2006) [http://partsregistry.org/Part:BBa_C0078]
+
::*[http://partsregistry.org/Part:BBa_C0078 BBa_C0078](2006)
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</tr>
</tr>
<tr>
<tr>
-
<td>dH2O</td>
+
<td>dH<sub>2</sub>O</td>
<td>28</td>
<td>28</td>
</tr>
</tr>
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</tr>
</tr>
<tr>
<tr>
-
<td>dH2O</td>
+
<td>dH<sub>2</sub>O</td>
<td>7</td>
<td>7</td>
</tr>
</tr>
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:From left;
:From left;
-
::*BBa_C0078(2007) [http://partsregistry.org/Part:BBa_C0078] -> None
+
::*[http://partsregistry.org/Part:BBa_C0078 BBa_C0078](2007) -> None
-
::*BBa_C0078(2006) [http://partsregistry.org/Part:BBa_C0078] -> None
+
::*[http://partsregistry.org/Part:BBa_C0078 BBa_C0078](2006) -> None
-
::*BBa_C0076(2007) [http://partsregistry.org/Part:BBa_C0076] -> None
+
::*[http://partsregistry.org/Part:BBa_C0076 BBa_C0076](2007) -> None
-
::*BBa_C0070(2007) [http://partsregistry.org/Part:BBa_C0070] -> OK
+
::*[http://partsregistry.org/Part:BBa_C0070 BBa_C0070](2007) -> OK
-
::*BBa_C0070(2006) [http://partsregistry.org/Part:BBa_C0070] -> OK
+
::*[http://partsregistry.org/Part:BBa_C0070 BBa_C0070](2006) -> OK
|}
|}
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:'''[[Team:Chiba/protocol/transformation|Transformation]]'''
:'''[[Team:Chiba/protocol/transformation|Transformation]]'''
:competent cells : XL10G
:competent cells : XL10G
-
::*BBa_S03154(2007) [http://partsregistry.org/Part:BBa_S03154]
+
::*[http://partsregistry.org/Part:BBa_S03154 BBa_S03154](2007)
-
::*BBa_S03154(2006) [http://partsregistry.org/Part:BBa_S03154]
+
::*[http://partsregistry.org/Part:BBa_S03154 BBa_S03154](2006)
-
::*BBa_I9026(2007) [http://partsregistry.org/Part:BBa_I9026]
+
::*[http://partsregistry.org/Part:BBa_I9026 BBa_I9026](2007)
-
::*BBa_I9026(2006) [http://partsregistry.org/Part:BBa_I9026]
+
::*[http://partsregistry.org/Part:BBa_I9026 BBa_I9026](2006)
-
::*BBa_I9030(2007) [http://partsregistry.org/Part:BBa_I9030]
+
::*[http://partsregistry.org/Part:BBa_I9030 BBa_I9030](2007)
-
::*BBa_I9030(2006) [http://partsregistry.org/Part:BBa_I9030]
+
::*[http://partsregistry.org/Part:BBa_I9030 BBa_I9030](2006)
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--->(23/8)'''[[Team:Chiba/protocol/digestion|Digestion]]'''
--->(23/8)'''[[Team:Chiba/protocol/digestion|Digestion]]'''
-
 
-
 
===Team:Output===
===Team:Output===

Revision as of 09:13, 24 October 2008

>Home | Notebook

20 August 2008 <|> 22 August 2008

Contents

Laboratory work

Team:Input

(-->20/8)pick transformants

  • [http://partsregistry.org/Part:BBa_R0051 BBa_R0051](2007)
  • [http://partsregistry.org/Part:BBa_R0051 BBa_R0051](2006)
  • [http://partsregistry.org/Part:BBa_J06650 BBa_J06650](2007)
  • [http://partsregistry.org/Part:BBa_J06650 BBa_J06650](2006)
  • [http://partsregistry.org/Part:BBa_J22136 BBa_J22136](2007)
  • [http://partsregistry.org/Part:BBa_J22141 BBa_J22141](2007)

を2ml培養、12h。ただしコロニーが1個だけだったBBa_J22141は2ml培養の11h後にIPTGを20μl加え、 さらに1h培養した。


  • UV照射実験(プレート編)(~24日)
  • two plasmids from ---
    • (Repressor)-Ptrc-LuxR-Plux-cI-colE1-Amp-
    • (Reporter)-PcI-GFP-p15a-Cm-(BW)
  1. Inoculated (Reporter) culture from glycerol stock(-80℃ freezer) in 2mL LB medium.(LB-Amp,Cm)(LB-Amp,Cm,AHL100nM)の2種類。


37℃で12h培養後、濁ったらそれぞれを105希釈してAHLが入っていないものはLB-Amp,Cm,AHLが入っているものはAHL-Amp,Cm,AHL100nMのプレートにそれぞれ20μl撒く。
37℃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℃,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
AHLなしAHL100nM
9h 606453
12h 146151


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
  • [http://partsregistry.org/Part:BBa_C0070 BBa_C0070](2007)
  • [http://partsregistry.org/Part:BBa_C0070 BBa_C0070](2006)
  • [http://partsregistry.org/Part:BBa_C0076 BBa_C0076](2007)
  • [http://partsregistry.org/Part:BBa_C0078 BBa_C0078](2007)
  • [http://partsregistry.org/Part:BBa_C0078 BBa_C0078](2006)


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


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


--->Gel Check
Chiba-0821.JPG
Sample DNA 3
Loading Dye 2
dH2O 7
TOTAL 12μL
From left;
  • [http://partsregistry.org/Part:BBa_C0078 BBa_C0078](2007) -> None
  • [http://partsregistry.org/Part:BBa_C0078 BBa_C0078](2006) -> None
  • [http://partsregistry.org/Part:BBa_C0076 BBa_C0076](2007) -> None
  • [http://partsregistry.org/Part:BBa_C0070 BBa_C0070](2007) -> OK
  • [http://partsregistry.org/Part:BBa_C0070 BBa_C0070](2006) -> OK


Transformation
competent cells : XL10G
  • [http://partsregistry.org/Part:BBa_S03154 BBa_S03154](2007)
  • [http://partsregistry.org/Part:BBa_S03154 BBa_S03154](2006)
  • [http://partsregistry.org/Part:BBa_I9026 BBa_I9026](2007)
  • [http://partsregistry.org/Part:BBa_I9026 BBa_I9026](2006)
  • [http://partsregistry.org/Part:BBa_I9030 BBa_I9030](2007)
  • [http://partsregistry.org/Part:BBa_I9030 BBa_I9030](2006)



--->(23/8)Digestion

Team:Output

Transformation

  • [http://partsregistry.org/Part:BBa_J32007 BBa_J32007](Lux CDABE)-->no colony
  • [http://partsregistry.org/Part:BBa_B0034 BBa_B0034](RBS)-->colony
結果:成功→RBS
失敗→Lux CDABE(二回行ったがどちらもコロニーができなかった)→三回目に成功