Team:HokkaidoU Japan/Notebook/August23

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=pSB1C3 Activity Check=
=pSB1C3 Activity Check=
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*Used 2 uL of from 100 uL of gel extracted DNA for liagation
*Used 2 uL of from 100 uL of gel extracted DNA for liagation
** Namely added 2 uL of Ligation Solution to 2 uL of DNA
** Namely added 2 uL of Ligation Solution to 2 uL of DNA
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*Incubated at 16C for 30min
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*Incubated at 16C for 30 min
===Ligation Negative Control===
===Ligation Negative Control===
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Used 2 uL of from 100 uL of gel extracted DNA for Transformation
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Used 2 uL of from 100 uL of gel extracted DNA for [[Team:HokkaidoU_Japan/Protocols|Transformation]]
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=Vector PCR: We meet again=
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=Vector PCR: We meet again!=
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[[Image:HokkaidoU Japan 20100823a.JPG‎|200px|right|thumb|]]
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[[Image:HokkaidoU Japan 20100823a.JPG‎|200px|right|thumb|Electrophoresis to check if PCR was succesful]]
Amplified pSB1A3, pSB1C3 and pSB1T3 by PCR as listed in the table bellow.
Amplified pSB1A3, pSB1C3 and pSB1T3 by PCR as listed in the table bellow.

Latest revision as of 08:30, 27 October 2010

pSB1C3 Activity Check

EcoR I/Pst I Digestion

Reagent Amount
pSB1C3 50 uL
DW 4 uL
0.1% BSA 7 uL
10x M Buffer 7 uL
EcoR I 1 uL
Pst I 1 uL
Total 70 uL
  • Incubated at 37C for 60 min
  • Added 15 uL of 6x Sample Buffer and electrophoresed on six lanes
  • Extracted from gel

Ligated

  • Used 2 uL of from 100 uL of gel extracted DNA for liagation
    • Namely added 2 uL of Ligation Solution to 2 uL of DNA
  • Incubated at 16C for 30 min

Ligation Negative Control

Used 2 uL of from 100 uL of gel extracted DNA for Transformation

Vector PCR: We meet again!

Electrophoresis to check if PCR was succesful

Amplified pSB1A3, pSB1C3 and pSB1T3 by PCR as listed in the table bellow.

Reagent Amount
Vector 1
DW 33
10x Buffer 5
2 M 4dNTPs 5
25 mM MgSO4 3
Suffix-F 1
Prefix-R 1
KOD 1
Total 50 uL
  • Only deviation from protocol was increase to extention to 120 sec