ATRX Antibody (5B3)

Immunocytochemistry/Immunofluorescence: ATRX Antibody (5B3) [H00000546-M03] - Analysis of monoclonal antibody to ATRX on HeLa cell. Antibody concentration 20 ug/ml

Product Discontinued

ATRX Antibody (5B3) Summary

• Description: Quality control test: Antibody Reactive Against Recombinant Protein.
• Immunogen: ATRX (NP_000480, 2311 a.a. ~ 2410 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa. FNLGALSAMSNQQLEDLINQGREKVVEATNSVTAVRIQPLEDIISAVWKENMNLSEAQVQALALSRQASQELDVKRREAIYNDVLTKQQMLISCVQRILM
• Specificity: ATRX - alpha thalassemia/mental retardation syndrome X-linked (RAD54 homolog, S. cerevisiae) (5B3)
• Isotype: IgG1 Kappa
• Clonality: Monoclonal
• Host: Mouse
• Gene: ATRX
• Purity: IgG purified

Applications/Dilutions

• Dilutions:
  • ELISA
  • Immunocytochemistry/ Immunofluorescence
  • Western Blot 1:500
• Application Notes: Antibody reactivity against Recombinant Protein with GST tag on ELISA and WB. GST tag alone is used as a negative control.

Packaging, Storage & Formulations

• Storage: Aliquot and store at -20C or -80C. Avoid freeze-thaw cycles.
• Buffer: In 1x PBS, pH 7.4
• Preservative: No Preservative
• Purity: IgG purified

Notes

This product is produced by and distributed for Abnova, a company based in Taiwan.

Alternate Names for ATRX Antibody (5B3)

• alpha thalassemia/mental retardation syndrome X-linked (RAD54 (S. cerevisiae)homolog)
• alpha thalassemia/mental retardation syndrome X-linked (RAD54 homolog, S.cerevisiae)
• alpha thalassemia/mental retardation syndrome X-linked
• ATP-dependent helicase ATRX
• ATR2
• DNA dependent ATPase and helicase
• EC 3.6.1
• EC 3.6.4.12
• helicase 2, X-linked
• Juberg-Marsidi syndrome
• MGC2094
• MRXHF1
• RAD54 homolog
• RAD54L
• SFM1
• SHS
• transcriptional regulator ATRX
• XH2RAD54
• X-linked helicase II
• X-linked nuclear protein
• XNPZNF-HX
• Zinc finger helicase
• Znf-HX

Background

The protein encoded by this gene contains an ATPase/helicase domain, and thus it belongs to the SWI/SNF family of chromatin remodeling proteins. The mutations of this gene are associated with an X-linked mental retardation (XLMR) syndrome most often accompanied by alpha-thalassemia (ATRX) syndrome. These mutations have been shown to cause diverse changes in the pattern of DNA methylation, which may provide a link between chromatin remodeling, DNA methylation, and gene expression in developmental processes. This protein is found to undergo cell cycle-dependent phosphorylation, which regulates its nuclear matrix and chromatin association, and suggests its involvement in the gene regulation at interphase and chromosomal segregation in mitosis. Multiple alternatively spliced transcript variants encoding distinct isoforms have been reported. [provided by RefSeq]

Limitations

This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.

Bioinformatics

• Gene Symbol: ATRX
• Entrez:
  • 546(Human)
• Uniprot:
  • NP_000480(Human)