GTX14937
WWOX2 antibody
Cannot supply to this region.
- SKU:
- GTX14937
- Additional Names:
- WW domain containing oxidoreductase , D16S432E , EIEE28 , FOR , FRA16D , HHCMA56 , PRO0128 , SCAR12 , SDR41C1 , WOX1
- Application:
- ELISA, WB
- Concentration:
- 0.5-0.75 mg/ml
- Physical State:
- Liquid
- Species Reactivity:
- Human
- Purification:
- Affinity Purified
- Storage Conditions:
- -20[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., 2-8[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., -20[o]C/-70[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted.
- Supplier:
- Genetex
- Host:
- Rabbit
- Reactivities:
- Human, Mouse
- Buffer:
- Tris/Glycine, 0.5% BSA, 30% Glycerol, 0.02% Sodium azide.
- Immunogen:
- Synthetic peptide corresponding to unique amino acid sequence on WWOX2 protein.
- Uniprot:
- Q9NZC7
- Synonyms:
- D16S432E;DEE28;EIEE28;FOR;FRA16D;fragile site FRA16D oxidoreductase;HHCMA56;PRO0128;SCAR12;SDR41C1;short chain dehydrogenase/reductase family 41C member 1;WOX1;WW domain-containing oxidoreductase;WW domain-containing protein WWOX
- Extra Details:
- This gene encodes a member of the short-chain dehydrogenases/reductases (SDR) protein family. This gene spans the FRA16D common chromosomal fragile site and appears to function as a tumor suppressor gene. Expression of the encoded protein is able to induce apoptosis, while defects in this gene are associated with multiple types of cancer. Disruption of this gene is also associated with autosomal recessive spinocerebellar ataxia 12. Disruption of a similar gene in mouse results in impaired steroidogenesis, additionally suggesting a metabolic function for the protein. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2014]
- Shipping Conditions:
- Blue Ice