Difference between revisions of "Protein-Lipid Overlay Assay"
From Bridges Lab Protocols
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# Wash the blots and incubate for 1hr at room temperature with a secondary antibody in 5% non-fat dry milk in TBS with 0.1% Tween20. | # Wash the blots and incubate for 1hr at room temperature with a secondary antibody in 5% non-fat dry milk in TBS with 0.1% Tween20. | ||
# Wash as in (5) & visualize the blot using Super-Signal chemiluminescent kit (Pierce). | # Wash as in (5) & visualize the blot using Super-Signal chemiluminescent kit (Pierce). | ||
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+ | [[ Category: Protein-Lipid Interactions ]] | ||
+ | [[ Category: Western Blot ]] |
Latest revision as of 20:55, 31 January 2011
from Emr Lab via Lois Weisman
- Prepare serial two-fold dilutions of PIP starting from 0.2mM dissolved in a resuspension solution of CHCl3:CH3OH:50mM HCl (5:10:4, v/v/v) with 2ml Ponceau S (Fluka 09276).
- Cut the proper size of nitrocellulose membrane (GE Water & Process Technologies, WP4HY00010).
- Spot 1ml of the PIP solution on the membrane.
- After drying blots in dark at room temperature (1 hr) & at 4oC (overnight), incubate the blot for 1hr at room temperature in a blocking solution (5% non-fat dry milk in TBS with 0.1% Tween20).
- Then incubate the blot overnight at 4oC with 5mg/ml the bacterial expressed and purified GST-fusion proteins in 0.5% fatty-acid free BSA (Sigma) in TBS with 0.1% Tween20.
- After washing 5 times each 5 minutes with TBS with 0.1% Tween20, incubate the blot overnight in a cold room with anti-GST antibody in a solution of 0.5% fatty-acid free BSA (Sigma) in TBS with 0.1% Tween20.
- Wash the blots and incubate for 1hr at room temperature with a secondary antibody in 5% non-fat dry milk in TBS with 0.1% Tween20.
- Wash as in (5) & visualize the blot using Super-Signal chemiluminescent kit (Pierce).