Team:Chiba/Calendar-Home/25 August 2008

From 2008.igem.org

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(Team:Input)
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<BR>Picked the colony and incubate with 2mL of LB-Ampicillin Medium for 12 hours at 37 degrees.
<BR>Picked the colony and incubate with 2mL of LB-Ampicillin Medium for 12 hours at 37 degrees.
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Took 180&mu;l from culture,and mixed with 880&um;lLB-Amp Medium.(OD=0.485)
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Took 180&mu;l from culture,and mixed with 880&mu;lLB-Amp Medium.(OD=0.485)
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Revision as of 00:15, 30 October 2008

>Home | Notebook

24 August 2008 <|> 26 August 2008

Contents

Laboratory work

Team:Input

The following glycerol Stock was made.

[http://partsregistry.org/Part:BBa_J22136 BBa_J22136](insert check OK)


Picked the colony and incubate with 2mL of LB-Ampicillin Medium for 12 hours at 37 degrees. Took 180μl from culture,and mixed with 880μlLB-Amp Medium.(OD=0.485)

Liquid culture(OD=0.495) 0.67μl
60%Glycerol 0.33μl
20%Glycerol Stock 1.00ml

Team:Communication

(24/8)--->Digestion
  1. Double Digestion:[http://partsregistry.org/Part:BBa_J04500 BBa_J04500](2007)
  2. Double Digesiton:[http://partsregistry.org/Part:BBa_R0010 BBa_R0010](2007)
  3. Single Digestion:[http://partsregistry.org/Part:BBa_R0010 BBa_R0010](2007)
  4. [http://partsregistry.org/Part:BBa_R0010 BBa_R0010](2007)
Sample No. 1234
Sample DNA 5511
EcoRI 0.50.5--
SpeI 0.50.5--
Buffer 1 11--
Buffer 3 --1-
BSA 11--
dH2O 227.5-
TOTAL 10μl10μl10μl1μl
--->Gel Check
Chiba-0825-1.JPG
Sample No. 1~34
Sample DNA 101
Loading Dye 21
dH2O -4
TOTAL 12μl6μl
From right;
  1. Double Digestion:[http://partsregistry.org/Part:BBa_J04500 BBa_J04500](2007) -> OK
  2. Double Digesiton:[http://partsregistry.org/Part:BBa_R0010 BBa_R0010](2007) -> ?(low)
  3. Single Digestion:[http://partsregistry.org/Part:BBa_R0010 BBa_R0010](2007) -> ?(low)
  4. [http://partsregistry.org/Part:BBa_R0010 BBa_R0010](2007) -> OK(low)


--->Digestion (Double Digestion)

  1. [http://partsregistry.org/Part:BBa_C0178 BBa_C0178]
  2. [http://partsregistry.org/Part:BBa_C0170 BBa_C0170]
  3. [http://partsregistry.org/Part:BBa_J04500 BBa_J04500](2007)
Sample No. 123
Sample DNA 33ng/μl×60μl33ng/μl×60μl100ng/μl×20μl
PstI 222
XbaI 22-
SpeI --2
Buffer 2 --5
Buffer 3 1010-
BSA 10105
dH2O 161616
TOTAL 100μl100μl52μl

Team:Output

PCR

  • [http://partsregistry.org/Part:BBa_E2030 BBa_E2030](1)
  • [http://partsregistry.org/Part:BBa_J33202 BBa_J33202](2)
  • BL21(3)
  • [http://partsregistry.org/Part:BBa_J52008 BBa_J52008](4)
  • [http://partsregistry.org/Part:BBa_I712019 BBa_I712019](5)
No. 12345
DNA tamplate 11111
FW primer 5(Venus_YFP_fwd)5(LacZ_fwd)5(LacZ_fwd)5(rLUC_fwd)5(fLuc_fwd)
VR primer 5(VR)5(LacZ_rev)5(LacZ_rev)5(VR)5(VR)
dNTPmix 1010101010
Thermo pol buffer 1010101010
DNA pol(VENT) 11111
dH2O 6868686868
TOTAL 100μl100μl100μl100μl100μl

-->Gel Check


No. 12345
DNA tamplate 11111
loading Dye 11111
dH2O 44444
TOTAL 6μl6μl6μl6μl6μl

Mini prep

  • [http://partsregistry.org/Part:BBa_E2030 BBa_E2030]
  • [http://partsregistry.org/Part:BBa_F2620 BBa_F2620]


Transformation

  • [http://partsregistry.org/Part:BBa_E2030 BBa_E2030]
  • PUC19
  • pGFPUV
  • pGEX Venus YFP
  • Membren Venus YFP

PCR

  • [http://partsregistry.org/Part:BBa_J63001 BBa_J63001](1)
No. 1
DNA tamplate 1
FW primer(Venus) 5
VR primer 5
dNTPmix 10
Thermo pol buffer 10
DNA pol(VENT) 1
dH2O 68
TOTAL 100μl