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BRWD3 Polyclonal Antibody, Invitrogen™
Rabbit Polyclonal Antibody
Brand: Invitrogen PA539065
This item is not returnable.
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Description
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].
Specifications
| BRWD3 | |
| Polyclonal | |
| Unconjugated | |
| BRWD3 | |
| BRWD3-H, BRWD3-I, BRWD3-K, BRWD3-P | |
| Rabbit | |
| Antigen affinity chromatography | |
| RUO | |
| 254065, 382236 | |
| -20°C | |
| Liquid |
| Immunohistochemistry (Paraffin), Western Blot | |
| 1 mg/mL | |
| Dulbecco′s PBS with 150mM NaCl, 50% glycerol and 0.02% sodium azide; pH 7.4 | |
| Q6RI45, A2AHJ4 | |
| BRWD3 | |
| A synthetic peptide derived from the internal region of human BRWD3 | |
| 100 μg | |
| Primary | |
| Human, Mouse | |
| Antibody | |
| IgG |
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