Team:Washington/Notebook

From 2009.igem.org

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*Purification
*Purification
 +
 +
==== Procedure ====
 +
# Set up overnights of parts 48-51
 +
# Dilute 1 ul overnight into 1ml
 +
# Add 1 mm IPTG and let grow for four hours
 +
# After cells have all grown up uniformly start boiling water for the boil step
 +
# Add 100uL of overnight to a 1.5mL tube
 +
# Pellet by spinning at max speed for 30 secs in the microcentrifuge
 +
# discard supernatent
 +
# Pull an aliquot of 5x sample loading buffer out of the freezer and thaw
 +
# Add 20uL BME to aliquot
 +
# Resuspend samples in 50uL sample loading buffer (pipette up/down)
 +
# Boil samples for 10 minutes
 +
# While boiling, prepare 500mL 1x SDS buffer:
 +
## 50mL 10x buffer to 450mL water
 +
## Take a gel out of the fridge and and put it in the gel box (keep the gel container for staining!!!)
 +
## Pour the mixed buffer solution into the half of the gel box that the gel is in
 +
## Remove the gel comb
 +
## Fill the little container on the top of the gel until it's about 0.5 cm from the top with buffer
 +
## Remove any bubbles in the wells
 +
# Spin down samples for a few seconds
 +
# Vortex samples
 +
# Load 3uL into each well
 +
# Load 10uL of ladder in appropriate wells
 +
# Run at 180V until the dye is about to fall off the gel
A ROUGH TIMELINE OF THE PROJECT!
A ROUGH TIMELINE OF THE PROJECT!
{{Template:Team:Washington/Templates/Footer}}
{{Template:Team:Washington/Templates/Footer}}

Revision as of 21:27, 12 October 2009

Uw title logo.png


A DETAILED DESCRIPTION OF THE PROTCOLS WE USED

  • Gene Synthesis
  • Colony PCR
  • Assembly
  • Cloning
  • Expression
  • Purification


Procedure

  1. Set up overnights of parts 48-51
  2. Dilute 1 ul overnight into 1ml
  3. Add 1 mm IPTG and let grow for four hours
  4. After cells have all grown up uniformly start boiling water for the boil step
  5. Add 100uL of overnight to a 1.5mL tube
  6. Pellet by spinning at max speed for 30 secs in the microcentrifuge
  7. discard supernatent
  8. Pull an aliquot of 5x sample loading buffer out of the freezer and thaw
  9. Add 20uL BME to aliquot
  10. Resuspend samples in 50uL sample loading buffer (pipette up/down)
  11. Boil samples for 10 minutes
  12. While boiling, prepare 500mL 1x SDS buffer:
    1. 50mL 10x buffer to 450mL water
    2. Take a gel out of the fridge and and put it in the gel box (keep the gel container for staining!!!)
    3. Pour the mixed buffer solution into the half of the gel box that the gel is in
    4. Remove the gel comb
    5. Fill the little container on the top of the gel until it's about 0.5 cm from the top with buffer
    6. Remove any bubbles in the wells
  13. Spin down samples for a few seconds
  14. Vortex samples
  15. Load 3uL into each well
  16. Load 10uL of ladder in appropriate wells
  17. Run at 180V until the dye is about to fall off the gel

A ROUGH TIMELINE OF THE PROJECT!

Retrieved from "http://2009.igem.org/Team:Washington/Notebook"