User:Michael F. Nagle/Notebook/Chem 571/2012/10/16: Difference between revisions

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**[[User:Keyun_Wang/Notebook/Experimental_Biological_Chemistry_I/2012/10/16|Keyun Wang]] prepared 100ng/uL solution of the matching forward primer.
**[[User:Keyun_Wang/Notebook/Experimental_Biological_Chemistry_I/2012/10/16|Keyun Wang]] prepared 100ng/uL solution of the matching forward primer.
**Solution was prepared with the following:  
**Solution was prepared with the following:  
***1uL forward primer ***1uL reverse primer ***1uL wild strand ADA ***5uL 10x Pfu buffer ***40.6uL molecular biology grade water ***1uL Turbo DNA polymerase solution ***0.4Turbo DNA polymerase 25mM dNTPs
***1uL forward primer  
***1uL reverse primer  
***1uL wild strand ADA  
***5uL 10x Pfu buffer  
***40.6uL molecular biology grade water  
***1uL Turbo DNA polymerase solution  
***0.4Turbo DNA polymerase 25mM dNTPs


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Revision as of 23:46, 6 December 2012

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Procedure

  • The procedure for PCR Mutation was followed
    • The specifications of the forward primer used are as follows:

    • 1mL molecular biology grade water was added to the primer.
    • The volume of primer solution needed to prepare 1mL of 100ng/uL solution was calculated
      • 0.49mg/1000μL = 490ng/μL
      • 100ng/uL*1000uL / 490ng/uL = 204.08μL
    • Keyun Wang prepared 100ng/uL solution of the matching forward primer.
    • Solution was prepared with the following:
      • 1uL forward primer
      • 1uL reverse primer
      • 1uL wild strand ADA
      • 5uL 10x Pfu buffer
      • 40.6uL molecular biology grade water
      • 1uL Turbo DNA polymerase solution
      • 0.4Turbo DNA polymerase 25mM dNTPs


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