CHAF1B Antibody (SS 24 1-68) - BSA Free
Novus Biologicals | Catalog # NB500-211
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Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.
Scientific Data Images for CHAF1B Antibody (SS 24 1-68) - BSA Free
Western Blot: CHAF1B Antibody (SS 24 1-68) [NB500-211]
Western Blot: CHAF1B Antibody (SS 24 1-68) [NB500-211] - Analysis of CAF-1 p60 expression in 1) HeLa and 2) Cos7 whole cell lysates using NB500-211.Immunocytochemistry/ Immunofluorescence: CHAF1B Antibody (SS 24 1-68) [NB500-211]
Immunocytochemistry/Immunofluorescence: CHAF1B Antibody (SS 24 1-68) [NB500-211] - Immunocytochemical staining of CAF-1 p60 in HeLa cells (Smith and Stillman 1991).Applications for CHAF1B Antibody (SS 24 1-68) - BSA Free
Immunocytochemistry/ Immunofluorescence
Immunoprecipitation
Western Blot
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Background: CHAF1B
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Product Documents for CHAF1B Antibody (SS 24 1-68) - BSA Free
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Product Specific Notices for CHAF1B Antibody (SS 24 1-68) - BSA Free
This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.
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Protocols
View specific protocols for CHAF1B Antibody (SS 24 1-68) - BSA Free (NB500-211):
Procedure Guide for Monoclonal anti- CAF-1 p60 (clone 24)
Catalog# NB 500-211
Immunoprecipitation Procedure
1) Cells were prepared in 0.4-1% NP-40 lysis buffer.
2) After osmotic shock and nuclear extractions of the cells, use the following buffer: 25mM Tris, 150mM NaCl, 1mM EDTA, 1mM DTT, and 0.01% NP-40.
3) Clarify the extracts with two successive 5 minute clearing spins (in a microfuge).
4) Preclear the extracts with some protein G beads (~20 ul).
5) Incubate the extracts with ~ 0.1-1ug of anti-CAF-1p60-24 [NB 500-211]/ control antibody for 1-3 hours.
6) Spin the antibody/extract for 5 minutes.
7) Incubate the antibody/extract with protein G beads, rotating for 1-2 hours.
8) Wash the beads, twice, for 5 minutes, at low ionic strength [150mM MaCl] in 1ml volume (*Optional: wash again, twice, at high ionic strength [ 400mM NaCl]).
9) Resuspend the washed beads in Laemlli sample buffer and boil for 5 minutes.
NOTE:
a. All steps for IP are performed at 4C.
b. CAF-1p60 is phosphorylated and contains a PEST sequence. Therefore, it is recommended that protease and phophatase inhibitors be added to all buffers.
c. The protocol for crosslinking CAF-1p60 to protein G beads was obtained from the Harlow and Lane book, Using Antibodies.
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