Team:DTU-Denmark/Notebook/7 June 2013

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(jfla)
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->in 1 of these L, 14 g of agar were added for making LB solid medium
->in 1 of these L, 14 g of agar were added for making LB solid medium
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==plating E.coli==
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===plating E.coli===
*Colonies of Top 10 E.coli were streaked on two plates
*Colonies of Top 10 E.coli were streaked on two plates
*Colonies of Top 10 + pZE21 em GFP were streaked on kanamycin-Agar -> 10 uL kan on each plate (LB + 30 ug/mL kan)
*Colonies of Top 10 + pZE21 em GFP were streaked on kanamycin-Agar -> 10 uL kan on each plate (LB + 30 ug/mL kan)

Revision as of 12:48, 23 July 2013

07 June 2013

Contents


lab 208


Main purposes today


  • helloworld-project
  • prepare solutions
  • autoclaving
  • plate E.coli

Who was in the lab


Kristian

Procedure


  1. 1M CaCl_2 (200ml) weighed off 22.206 g CaCl_2
  2. 50% glycerol (500 ml)
  3. LB medium (liquid) (3 L);

->20 g of LB in every 1 L of distilled water. Autoclaved medium

->in 1 of these L, 14 g of agar were added for making LB solid medium

plating E.coli

  • Colonies of Top 10 E.coli were streaked on two plates
  • Colonies of Top 10 + pZE21 em GFP were streaked on kanamycin-Agar -> 10 uL kan on each plate (LB + 30 ug/mL kan)

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