Procedure for Stripping an Immunoblot using Pierce Restore Stripping Buffer
You also can try our home made stripping buffer--2%
Sodium Docecyl Sulfate (SDS), 10mM 2-Mercaptomethanol, 62.5mM Trizma base,pH 6.7--with the same procedure as follows.
Notes:Blots that cannot be stripped immediately after chemiluminescent detection may be stored in phosphate buffered saline (PBS) at 4C
until the stripping procedure can be performed.
1. Warm bottle of Restore Western Blot Stripping Buffer to room temperature.
2.
Place the blot to be stripped in Restore Western Blot Stripping Buffer and incubate for 5-15 minutes at room temperature. Use a sufficient
volume to ensure that the blot is completely wetted (i.e.,approximately 10 ml).
Note: Optimization of both incubation time and temperature
is essential for best results. In general, higher affinity antibodies will require at least 15 minutes of stripping and may require
an incubation temperature of 37C.
3. Remove the blot from the Restore Western Blot Stripping Buffer and wash in Wash Buffer.
4.
Test for complete removal of the HRP label (e.g., secondary antibody): Incubate the membrane with new chemiluminescent detection reagent
and expose to film. If no signal is detected using a 5-minute exposure, the HRP conjugate has been successfully removed from the antigen
or primary antibody.
5. If signal is detected return to step 2, stripping for an additional 5-15 minutes. Some antigen/antibody
systems require increased temperature and/or longer incubation times to strip them fully. Optimize stripping time and temperature
to ensure complete removal of antibodies while preventing damage to the antigen.
6. After determining that the membrane is properly
stripped, the second immunoprobing experiment may be performed.
Notes: Blot may be stripped and reprobed several times but may
require longer exposure times or a more sensitive chemiluminescent substrate. Subsequent reprobings may result in decreased signal
if the antigen is labile in Stripping Buffer. Analysis of the individual system is required.
Reblocking a membrane is usually
not necessary after stripping but may be required in some applications.
Western Blot Hybridization Center
Western Blot Full Procedure (from Pierce)
Western Blotting Procedure with Video Show
Protocol
1: Western Blot 1
2) Protein concentration assay
3) Electrophoresis and blotting
4)Blocking
non-specific antigen
5) Incubation with primary antibody
6) Incubation with secondary antibody
Restore
a western blot using pierce stripping buffer
Western blot related solutions and buffers
Protocol
2: Western Blot 2.
Protocol 3: Western Blot 3.
More online Western blot protocols
Web Guider
Ch 8.Immunohistoch / immunology
Ch 10.GC/MS, NMR and Proteomics