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Mouse Monoclonal Anti-CHD4 antibody (STJ99175)
Supplier: St John’s Laboratory Ltd.
Recommended applications: WB, ELISA
Recommended dilution: WB 1:500-2000; ELISA 1:10000-20000
Recommended protocols: check protocols
Click or hover above images to see image description for Anti-CHD4 antibody.
Check alternative names for the antibodyExpand
|ATP dependent helicase CHD4 antibody|ATP-dependent helicase CHD4 antibody|CHD 4 antibody|CHD-4 antibody|CHD4 antibody|CHD4_HUMAN antibody|Chromodomain helicase DNA binding protein 4 antibody|Chromodomain-helicase-DNA-binding protein 4 antibody|Mi 2 autoantigen 218 kDa protein antibody|Mi 2b antibody|Mi-2 autoantigen 218 kDa protein antibody|Mi2 beta antibody|Mi2-beta antibody|Anti-CHD4 antibody [3F2/4] – ChIP Grade (ab70469)
SCBT cat No: sc-55606|sc-11378|sc-81323|sc-12547|sc-8774|sc-365638|sc-365639|sc-393647|sc-373820|
|Catalogue No.|| |
Anti-CHD4 antibody detects endogenous levels of CHD4 and does not cross-react with related proteins.
Purified recombinant human CHD4 protein fragments expressed in E.coli.
|Recommended dilution|| |
WB 1:500-2000; ELISA 1:10000-20000
|Molecular weight|| |
Anti-CHD4 antibody was tube-contained in liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Anti-CHD4 antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
-20 Celsius degree. Avoid repeated freeze/thaw cycles.
|Alternative antibody names|| |
ATP dependent helicase CHD4 antibody, ATP-dependent helicase CHD4 antibody, CHD 4 antibody, CHD-4 antibody, CHD4 antibody, CHD4_HUMAN antibody, Chromodomain helicase DNA binding protein 4 antibody, Chromodomain-helicase-DNA-binding protein 4 antibody, Mi 2 autoantigen 218 kDa protein antibody, Mi 2b antibody, Mi-2 autoantigen 218 kDa protein antibody, Mi2 beta antibody, Mi2-beta antibody
|Database links|| |
|Protein function|| |
Component of the histone deacetylase NuRD complex which participates in the remodeling of chromatin by deacetylating histones. .
|Involvement in disease|| |
Sifrim-Hitz-Weiss syndrome (SIHIWES) [MIM:617159]: An autosomal dominant syndrome characterized by mental retardation, variable congenital defects affecting cardiac, skeletal, and urogenital systems. Short stature, macrocephaly, hearing impairment, and facial dysmorphism are present in some patients. . Note=The disease is caused by mutations affecting the gene represented in this entry.
|Protein sequence and domain|| |
Belongs to the SNF2/RAD54 helicase family. ; Contains 2 chromo domains. ; Contains 1 helicase ATP-binding domain. ; Contains 1 helicase C-terminal domain. ; Contains 2 PHD-type zinc fingers.
|Protein cellular localization|| |
Nucleus . Cytoplasm, cytoskeleton, microtubule organizing center, centrosome . Note=Associates with centrosomes in interphase. .
|Research area|| |
<a href="http://antibodyplus.com/research-areas/">All research areas</a>><a href="http://antibodyplus.com/Transcription-Regulators/">Transcription Regulators</a>><a href="http://antibodyplus.com/product-tag/Mi2/">Mi2</a><br><a href="http://antibodyplus.com/product-tag/Transcription-Regulators/"> (View all antibody categories related to Transcription Regulators)</a>
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St John’s Laboratory Ltd.
|Product type|| |
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