Team:DTU-Denmark/Notebook/4 July 2013

From 2013.igem.org

(Difference between revisions)
(Procedure)
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==Procedure==
==Procedure==
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==Preparation of SOB medium==
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==Preparation of SOB medium==
  Total volume 1 L
  Total volume 1 L
  * 5 g yeast extract
  * 5 g yeast extract
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  * 2.41 g MgSO4  
  * 2.41 g MgSO4  
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==Preparation of CCMB80 buffer (500 ml)==
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==Preparation of CCMB80 buffer (500 ml)==
  * KOAc :5 ml (0.98 gr)
  * KOAc :5 ml (0.98 gr)
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  * 10% glycerol (50 ml)
  * 10% glycerol (50 ml)
  Adjustment of pH (6.37) with 0.1 HCl
  Adjustment of pH (6.37) with 0.1 HCl
-
 
==Preparation of LB agar==
==Preparation of LB agar==

Revision as of 20:17, 7 July 2013

Contents

301

main purpose

We want to view our cells throught a fluorescent microscope, in order to see if they have expressed GFP and RPF.

Hopefully we will see GFP in the periplasm and RFP inside the cell.

Setup an overnight culture of the 2 successful transformants so we can both MidiPrep and isolate periplasmic proteins tomorrow.


Procedure

Results

We managed to see expressed GFP and RFP


115

main purpose

Preparation for making competent cells based on the protocol ([http://parts.igem.org/Help:Protocols/Competent_Cells]).

Who was in the lab


Henrike, Ariadni, Kashia, Natalia

Procedure

Preparation of SOB medium

Total volume 1 L
* 5 g yeast extract
* 20.05 g tryptone
* 0.58 g NaCl
* 0.19 g KCl
* 2.41 g MgSO4 

Preparation of CCMB80 buffer (500 ml)

* KOAc :5 ml (0.98 gr)
* CaCl2.2H2O (5.9 g)
* MnCl2.4H2O (2 g)
* MgCl2.6H2O (1 g) 
* 10% glycerol (50 ml)
Adjustment of pH (6.37) with 0.1 HCl

Preparation of LB agar

Conclusion from today

Cultivation of TOP10 cells in SOB

* 1 loop of TOP10 cells (from 14.06.2013)
* 10 ml of SOB medium
Incubate for 16 hours in 24 degrees and 37 degrees.