Team:DTU-Denmark/Notebook/7 June 2013
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- | == | + | {{:Team:DTU-Denmark/Templates/StartPage|07 June 2013}} |
+ | |||
+ | =lab 208= | ||
+ | <hr/> | ||
+ | == Main purposes today == | ||
+ | <hr/> | ||
*helloworld-project | *helloworld-project | ||
*prepare solutions | *prepare solutions | ||
- | *[[Team:DTU-Denmark/Methods/ | + | *[[Team:DTU-Denmark/Methods/Autoclaving|autoclaving]] |
- | == | + | *plate ''E.coli'' |
+ | |||
+ | ==Who was in the lab== | ||
+ | <hr/> | ||
Kristian | Kristian | ||
==Procedure== | ==Procedure== | ||
+ | <hr/> | ||
#1M CaCl_2 (200ml) weighed off 22.206 g CaCl_2 | #1M CaCl_2 (200ml) weighed off 22.206 g CaCl_2 | ||
- | #50% glycerol ( | + | #50% glycerol (500 ml) |
+ | #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) | ||
+ | |||
+ | Navigate to the [[Team:DTU-Denmark/Notebook/5_June_2013|Previous]] or the [[Team:DTU-Denmark/Notebook/9_June_2013|Next]] Entry | ||
+ | |||
+ | {{:Team:DTU-Denmark/Templates/EndPage}} |
Latest revision as of 20:59, 16 September 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
- 1M CaCl_2 (200ml) weighed off 22.206 g CaCl_2
- 50% glycerol (500 ml)
- 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)
Navigate to the Previous or the Next Entry