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BAZ1B antibody
BAZ1B
Reactivity: Human
WB
Host: Rabbit
Monoclonal
unconjugated
Product Details anti-BAZ1B Antibody
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Target
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BAZ1B
(Bromodomain Adjacent To Zinc Finger Domain, 1B (BAZ1B))
Reactivity
All reactivities for BAZ1B antibodies
Human
Host
All hosts for BAZ1B antibodies
Rabbit
Clonality
All clonalities for BAZ1B antibodies
Monoclonal
Conjugate
All conjugates for BAZ1B antibodies
This BAZ1B antibody is un-conjugated
Application
All applications for BAZ1B antibodies
Western Blotting (WB)
Purpose
WSTF Rabbit mAb
Cross-Reactivity
Human, Mouse, Rat
Characteristics
Monoclonal Antibodies
Purification
Affinity purification
Immunogen
A synthesized peptide derived from human WSTF
Isotype
IgG
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Discover our top product BAZ1B Primary Antibody
Alternatives
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Application Details
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Application Notes
WB,1:500 - 1:2000
Restrictions
For Research Use only
Handling
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Format
Liquid
Buffer
PBS with 0.02 % sodium azide,0.05 % BSA,50 % glycerol, pH 7.3.
Preservative
Sodium azide
Precaution of Use
This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Storage
-20 °C
Storage Comment
Store at -20°C. Avoid freeze / thaw cycles.
Target Details for BAZ1B
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Target
BAZ1B
(Bromodomain Adjacent To Zinc Finger Domain, 1B (BAZ1B))
Alternative Name
BAZ1B (BAZ1B Products )
Synonyms
BAZ1B antibody, wstf antibody, wbscr9 antibody, wbscr10 antibody, LOC100220420 antibody, WBSCR10 antibody, WBSCR9 antibody, WSTF antibody, C87820 antibody, Wbscr9 antibody, fi60d02 antibody, im:7137554 antibody, wu:fi60d02 antibody, bromodomain adjacent to zinc finger domain 1B antibody, bromodomain adjacent to zinc finger domain, 1B antibody, bromodomain adjacent to zinc finger domain 1B S homeolog antibody, BAZ1B antibody, baz1b antibody, Baz1b antibody, baz1b.S antibody
Background
This gene encodes a member of the bromodomain protein family. The bromodomain is a structural motif characteristic of proteins involved in chromatin-dependent regulation of transcription. This gene is deleted in Williams-Beuren syndrome, a developmental disorder caused by deletion of multiple genes at 7q11.23. [provided by RefSeq, Jul 2008],WBSCR10, WBSCR9, WSTF,Chromatin Remodeling,Epigenetic writers and erasers of core Histones,Epigenetic writers and erasers of core Histones_Phosphorylation,Epigenetics & Nuclear Signaling,Kinase,Signal Transduction,BAZ1B
Molecular Weight
185kDa
Gene ID
9031
UniProt
Q9UIG0
Pathways
Nuclear Hormone Receptor Binding , Chromatin Binding
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