Difference between revisions of "User:Michael F. Nagle/Notebook/Chem 571/2012/11/06"

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(Procedure)
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**Single 200μL plates were prepared. No 50μL plates were made.
 
**Single 200μL plates were prepared. No 50μL plates were made.
 
**Plates were incubated at 37<sup>o</sup>C
 
**Plates were incubated at 37<sup>o</sup>C
*Adenosine Deaminase prepared [[User:Michael_F._Nagle/Notebook/Chem_571/2012/10/23|Oct. 23]] was purified via FPLC [User:Michael_F._Nagle/Notebook/Chem_571/2012/09/26|as was done 9/26]]
+
*Adenosine Deaminase prepared [[User:Michael_F._Nagle/Notebook/Chem_571/2012/10/23|Oct. 23]] was purified via FPLC [[User:Michael_F._Nagle/Notebook/Chem_571/2012/09/26|as was done 9/26]]
 
** Pump flow was 5mL/minute
 
** Pump flow was 5mL/minute
  

Revision as of 03:33, 7 December 2012

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Objectives

  • Transform Adenosine Deaminase in cells
  • Purify protein via Fast Protein Liquid Chromatography (FPLC)

Procedure

  • The prodedure for transformation was followed, just like on 10/24 but with the following modifications
    • 20μL DNA solution was added to 30μL solution with E. Coli cells.
    • 250μL Lysogeny Broth (LB) was used instead of SOC medium.
    • Single 200μL plates were prepared. No 50μL plates were made.
    • Plates were incubated at 37oC
  • Adenosine Deaminase prepared Oct. 23 was purified via FPLC as was done 9/26
    • Pump flow was 5mL/minute