Team:ESBS-Strasbourg/10 July 2008

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(Difference between revisions)
(WetLab)
 
Line 13: Line 13:
** Transformation (db3.1) with positive and negative control and BB_p1010 in Amipicillin and in Kanamycin backround
** Transformation (db3.1) with positive and negative control and BB_p1010 in Amipicillin and in Kanamycin backround
* Sandra:  
* Sandra:  
-
** resuspend primer to stock solutions of 50 µM
+
** resuspension of primers to stock solutions of 50 µM
** making primer aliquots of 10 µM (4x 50 µl)
** making primer aliquots of 10 µM (4x 50 µl)
-
** transformation (dh5alpha cells) with positiv and negative control and BioBrick GFP-device
+
** transformation (dh5alpha cells) with positive and negative control and BioBrick GFP-device
* MM:  
* MM:  
** TSB-Buffer
** TSB-Buffer

Latest revision as of 12:26, 16 July 2008

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Contents

DryLab

  • MM: Sponsoring
  • michi:
    • design of the oligos to construct the operons of our DNA Binding Proteins.
    • design of the promoter region: get CMV minimal promoter

Modeling

WetLab

  • Katja:
    • Preparation of LB liquid media and LB(A) plates
    • Transformation (db3.1) with positive and negative control and BB_p1010 in Amipicillin and in Kanamycin backround
  • Sandra:
    • resuspension of primers to stock solutions of 50 µM
    • making primer aliquots of 10 µM (4x 50 µl)
    • transformation (dh5alpha cells) with positive and negative control and BioBrick GFP-device
  • MM:
    • TSB-Buffer
    • Made competent cells (TOP10, db3.1, dh5alpha)
    • Transformation (TOP10)

General

Quote of the day

MW: "I always got heavy beard growth -roarr"