User:Wilfred J. Poppinga/Notebook/cAMP compartmentalization/2010/03/15: Difference between revisions

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===Coating of ELISA plate===
===Coating of ELISA plate===
* Mix
* Mix
** 24 mL coating buffer
** 24 mL coating buffer (date of preparation 11March2010)
** 80 μL primary antibody
** 80 μL primary antibody
* Add 100 μL per well (96-wells plate)
* Add 100 μL per well (96-wells plate)

Revision as of 06:25, 15 March 2010

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Summary

  • Co-IP
    • Cell lysation
    • Preparation of beads
  • S0 24-wells
  • Coat ELISA Plate


Materials & Methods

Materials

Method

Putting cells to S0

  • Wash cells twice with PBS
  • Add 500 μL DMEM S0 to each well
  • Incubate @ 37 °C

Determination of protein concentration

  • Use cells on S+ refreshed 12March2010
    • 1 Ø 10 cm dish each donor
  • Put cells on ice
  • Remove medium
  • Wash twice with 5 mL cold PBS
  • Add 1 mL RIPA buffer
  • Scrape of cells and collect in 1.5 mL tube
  • Sonicate (4x short pulse)
  • Take 10 μL of undiluted and a 5x diluted samples for Bradford assay (Pierce determination)
  • Store samples @ -20 °C

Co-immunoprecipitation part I

  • Beads were coated with anti-PKA antibodies.
  • For 2 samples (D9/D12; Only Beads, Beads with Antibody, Beads w. AB & RIPA and Bead w. AB & Sample)
    • 280 μL beads
    • Spin down and remove EtOH
    • Wash with excess (400 μL) PBS
    • Spin down and remove PBS
    • Add 1:1 PBS:Beads (280 μL)
      • 200 μL for Beads with Antibody, Beads w. AB & RIPA and Bead w. AB & Sample (D9/D12)
      • 80 μL for Only Beads (D9/D12)
      • (30 μL for each condition)
    • Add 1:100 antibody (or not for control), 2 μL
    • Incubate ON @ 4 °C

Coating of ELISA plate

  • Mix
    • 24 mL coating buffer (date of preparation 11March2010)
    • 80 μL primary antibody
  • Add 100 μL per well (96-wells plate)
  • Incubate ON


96-wells plate ELISA
# 01 02 03 04 05 06 07 08 09 10 11 12
A
B
C
D
E
F
G
H
I

Notes

Results

  • PIERCE

Conclusion

  • DONE Ow..