Transcriptional regulator ATRX (EC 3.6.4.12; UniProt P46100; also known as Alpha thalassemia/mental retardation syndrome X-linked, ATP-dependent helicase ATRX, DNA dependent ATPase and helicase, Helicase 2 X-linked, X-linked helicase II, X-linked nuclear protein, XNP, Zinc finger helicase, Znf-HX) is encoded by the PRF1 (Also known as ATR2, JMS, MRXHF1, RAD54, RAD54L, SFM1, SHS, XH2, XNP, ZNF-HX) gene in human (Gene ID 546). Rad54 belongs to the SWI/SNF family of chromatin remodeling proteins. Rad54 undergoes cell cycle-dependent phosphorylation, nuclear matrix and chromatin association, and is implicatetd in playing a role in gene regulation during interphase and mitosis. ATRX mutations are associated with an X-linked mental retardation (XLMR) syndrome. most often accompanied by alpha-thalassemia syndrome, as a result of diverse changes in DNA methylation.

~283 kDa observed

Epitope: N-terminus

Recombinant protein corresponding to the N-terminus of human ATRX.

Anti-ATRX Antibody, clone 23C is an antibody against ATRX for use in Western Blotting and Immunocytochemistry.

Research Category
Epigenetics & Nuclear Function

Research Sub Category
Nuclear Receptors

Western Blotting Analysis: A representative lot detected ATRX in nuclear extracts from EBV-transformed lymphocytes (McDowell, T.L., et al. (1999). PNAS. 96(24):13983-13988).
Immunocytochemistry Analysis: A representative lot detected nuclear localization of ATRX in HeLa and L929 cells (McDowell, T.L., et al. (1999). PNAS. 96(24):13983-13988).

Protein G Purified

Format: Purified

Purified mouse monoclonal IgG1κ in buffer containing 0.1 M Tris-Glycine (pH 7.4), 150 mM NaCl with 0.05% sodium azide.

Stable for 1 year at 2-8°C from date of receipt.

Evaluated by Western Blotting in HeLa cell lysate.

Western Blotting Analysis: 2.0 µg/mL of this antibody detected ATRX in 10 µg of HeLa cell lysate.

Concentration: Please refer to lot specific datasheet.

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