Team:Aachen/TestBench2

From 2014.igem.org

(Difference between revisions)
m (LB medium)
m (LB medium)
Line 7: Line 7:
# weight components
# weight components
::* '''5 g/L NaCl'''
::* '''5 g/L NaCl'''
-
::# '''10 g/L tryptone'''
+
::* '''10 g/L tryptone'''
::* '''5 g/L yeast extract'''
::* '''5 g/L yeast extract'''
::* (15 g/L agar for plates)
::* (15 g/L agar for plates)
# fill up to 1 L with deionized water
# fill up to 1 L with deionized water
-
# '''mix well''' by shaking
+
* '''mix well''' by shaking
# autoclave
# autoclave
## autoclaving tape, caps slightly unscrewed
## autoclaving tape, caps slightly unscrewed

Revision as of 22:35, 17 September 2014

Contents


Media

LB medium

  1. weight components
  • 5 g/L NaCl
  • 10 g/L tryptone
  • 5 g/L yeast extract
  • (15 g/L agar for plates)
  1. fill up to 1 L with deionized water
  • mix well by shaking
  1. autoclave
    1. autoclaving tape, caps slightly unscrewed
    2. base of the pot has to be covered with deionized water
    3. close lid
    4. heat level 3 until the pressure valve opens
    5. reduce heat level to 1.5
    6. set timer to 20 minutes
    7. turn heater off
    8. wait until the pressure valve retracts (30-45 minutes)
    9. open, close caps & shake
  2. for plates, wait until you can touch the bottle (<60 °C, clean bench!)
  3. add antibiotics and shake (gloves!)

Hartmans minimal medium (HM)

Agar Chips

Transformation

Heat Shock

  1. thaw cells on ice
  2. add 1 µl of plasmid DNA
  3. incubate on ice for 30'
  4. heat shock at 42 °C for 60
  5. incubate on ice for 5'
  6. add 200 µl of SOC media
  7. incubate at 37 °C for 2 h
  8. plate 20  and 200 µl on plates with the appropiate antibiotic

Electroporation

PCR

Colony PCR

QuikChange

Clonings

Restriction Digest

Ligation

Gibson Assembly