User:Jose Fabricio Lopez/Notebook/GEDF/Protocols: Difference between revisions

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(New page: __TOC__ =Protocols= ==DNA== ===Transformation===)
 
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=Protocols=
=Protocols=
==DNA==
==DNA==
===Transformation===
===Transformation for E. Coli by electrophoration===
'''Reagent and instruments'''
*LB medium Liquid
*LB medium Solid
*DNA of plasmid. (10μL)
*Electrocompetent cells.
*Ice.
*Deionized water.
*Paper for deinization.
*Antibiotic
 
====''Instrucctions''====
 
1.-Introduce cells in DNA solution.
 
2.-Put cells in ice.
 
3.-Select Cuvettes for electroporation and put voltage. Wait until sound occurs.
 
4.-Put 500μL of LB liquid (without antibiotic).
 
5.-Grow up cells by 1 hour at 37°C mixing.
 
6.-Petri dishes with antibiotic.
 
7.-Plate cells.
 
'''Remember:''' Use controls for medium and cells.

Revision as of 16:51, 9 January 2012

Protocols

DNA

Transformation for E. Coli by electrophoration

Reagent and instruments

  • LB medium Liquid
  • LB medium Solid
  • DNA of plasmid. (10μL)
  • Electrocompetent cells.
  • Ice.
  • Deionized water.
  • Paper for deinization.
  • Antibiotic

Instrucctions

1.-Introduce cells in DNA solution.

2.-Put cells in ice.

3.-Select Cuvettes for electroporation and put voltage. Wait until sound occurs.

4.-Put 500μL of LB liquid (without antibiotic).

5.-Grow up cells by 1 hour at 37°C mixing.

6.-Petri dishes with antibiotic.

7.-Plate cells.

Remember: Use controls for medium and cells.