Team:Tokyo Metropolitan/Notebook

From 2011.igem.org

(Difference between revisions)
(PCR (PrimeSTAR® HS DNA Polymerase))
(PCR (PrimeSTAR® HS DNA Polymerase))
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=Lab Protocols=
=Lab Protocols=
==PCR (PrimeSTAR® HS DNA Polymerase)==
==PCR (PrimeSTAR® HS DNA Polymerase)==
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**Ice
+
*Ice
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**Micro pipette
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*Micro pipette**Thermal cycler  
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**Thermal cycler  
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*PCR Tube
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**PCR Tube
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*Micro Tube
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**Micro Tube
+
*DW
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**DW
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*5× PCR Buffer
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**5× PCR Buffer
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*dNTP (2.5mM)
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**dNTP (2.5mM)
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*Primer(Forward & Reverse)  (20µM)
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**Primer(Forward & Reverse)  (20µM)
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*Template DNA
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**Template DNA
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*PrimeSTAR® HS DNA Polymerase (2.5U/μl)
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**PrimeSTAR® HS DNA Polymerase (2.5U/μl)
+

Revision as of 08:29, 4 October 2011

Contents

Lab Notebook

Augast
Sun Mon Tue Wed Thu Fri Sat
1 2 3 4 5 6
7 8 9 10 11 12 13
14 15 16 17 18 19 20
21 22 23 24 25 26 27
28 29 30 31
September
Sun Mon Tue Wed Thu Fri Sat
1 2 3
4 5 6 7 8 9 10
11 12 13 14 15 16 17
18 19 20 21 22 23 24
25 26 27 28 29 30
Octorber
Sun Mon Tue Wed Thu Fri Sat
1
2 3 4 5 6


Lab Protocols

PCR (PrimeSTAR® HS DNA Polymerase)

  • Ice
  • Micro pipette**Thermal cycler
  • PCR Tube
  • Micro Tube
  • DW
  • 5× PCR Buffer
  • dNTP (2.5mM)
  • Primer(Forward & Reverse)  (20µM)
  • Template DNA
  • PrimeSTAR® HS DNA Polymerase (2.5U/μl)


  1. 以下の組成で、DW→Buffer→dNTP→primer→Template DNA→polymeraseの順に混ぜていく。反応液の調製は氷上で行う。Template DNAが液体の場合、その分DWの量を減らす。
  2. 良く撹拌(×ボルテックス)した後、氷上のPCR Tubeに分注する(50µlずつ)
  3. Thermal cyclerにセットし、RUNする。
    • 98℃・・・10sec
    • 55℃・・・5 or 15sec
    • 72℃・・・1min×1kbpごと 30cycle
  4. 反応終了後、電気泳動にて結果を観察 or 4℃で保存。

Electrophoresis

Ethanol precipitation

Plasmid Extraction

Digestion

Ligation

Transformation

Colony PCR

Making Medium for Culture

Making Gel for Electrophoresis