Team:Chiba/Calendar-Home/25 August 2008

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24 August 2008 <|> 26 August 2008

Contents

Laboratory work

Team:Input

The following glycerol Stock was made.

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:BBa_J04500(2007)
  2. Double Digesiton:BBa_R0010(2007)
  3. Single Digestion:BBa_R0010(2007)
  4. BBa_R0010(2007)
Sample No. 1234
Sample DNA(μL) 5511
EcoRI(μL) 0.50.5--
SpeI(μL) 0.50.5--
Buffer 1 11--
Buffer 3(μL) --1-
BSA(μL) 11--
dH2O(μL) 227.5-
TOTAL(μL) 1010101
--->Gel Check
Chiba-0825-1.JPG
Sample No. 1~34
Sample DNA(μL) 101
Loading Dye(μL) 21
dH2O(μL) -4
TOTAL(μL) 126
From right;
  1. Double Digestion:BBa_J04500(2007) -> OK
  2. Double Digesiton:BBa_R0010(2007) -> ?(low)
  3. Single Digestion:BBa_R0010(2007) -> ?(low)
  4. BBa_R0010(2007) -> OK(low)


--->Digestion (Double Digestion)

  1. BBa_C0178
  2. BBa_C0170
  3. BBa_J04500(2007)
Sample No. 123
Sample DNA(μL) 33ng/μl×60μl33ng/μl×60μl100ng/μl×20μl
PstI(μL) 222
XbaI(μL) 22-
SpeI(μL) --2
Buffer 2(μL) --5
Buffer 3(μL) 1010-
BSA(μL) 10105
dH2O(μL) 161616
TOTAL(μL) 10010052

Team:Output

PCR

No. 12345
DNA tamplate(μL) 11111
FW primer(μL) 5(Venus_YFP_fwd)5(LacZ_fwd)5(LacZ_fwd)5(rLUC_fwd)5(fLuc_fwd)
VR primer(μL) 5(VR)5(LacZ_rev)5(LacZ_rev)5(VR)5(VR)
dNTPmix(μL) 1010101010
Thermo pol buffer(μL) 1010101010
DNA pol(VENT)(μL) 11111
dH2O(μL) 6868686868
TOTAL(μL) 100100100100100

-->Gel Check


No. 12345
DNA tamplate(μL) 11111
loading Dye(μL) 11111
dH2O(μL) 44444
TOTAL(μL) 66666

Mini prep


Transformation

  • BBa_E2030
  • PUC19
  • pGFPUV
  • pGEX Venus YFP
  • Membren Venus YFP

PCR

No. 1
DNA tamplate(μL) 1
FW primer(Venus)(μL) 5
VR primer(μL) 5
dNTPmix(μL) 10
Thermo pol buffer(μL) 10
DNA pol(VENT)(μL) 1
dH2O(μL) 68
TOTAL(μL) 100