Team:DTU-Denmark/Notebook/4 July 2013

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== Conclusion from today==
== Conclusion from today==
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Cultivation of TOP10 cells in SOB
Cultivation of TOP10 cells in SOB
* 1 loop of TOP10 cells (from 14.06.2013)
* 1 loop of TOP10 cells (from 14.06.2013)

Revision as of 13:20, 25 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

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Main purpose

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

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.


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