BRWD3 rabbit pAb
The protein encoded by this gene contains a bromodomain and several WD repeats. It is thought to have a chromatin-modifying function, and may thus play a role in transcription. Mutations in this gene cause mental retardation X-linked type 93, which is also referred to as mental retardation X-linked with macrocephaly. This gene is also associated with translocations in patients with B-cell chronic lymphocytic leukemia. [provided by RefSeq, May 2010],
Product Specifications
Background
UniProt
Q6RI45
Swiss Prot
Q6RI45
Reactivity
Human; Mouse
Immunogen
The antiserum was produced against synthesized peptide derived from human BRWD3. AA range:1751-1800
Clonality
Polyclonal
Source
Rabbit
Applications
WB; IHC; IF; ELISA
Concentration
1 mg/ml
Dilution
Western Blot: 1/500 - 1/2000. Immunohistochemistry: 1/100 - 1/300. ELISA: 1/40000. Not yet tested in other applications.
Molecular Weight
204kD
Storage Conditions
-20°C/1 year
Observed Molecular Weight
204kD
Fragment
IgG
Subcellular Location
Nucleus
Other Product Names
BRWD3; Bromodomain and WD repeat-containing protein 3
Gene ID (Human)
254065
Available Sizes
Frequently Asked Questions
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