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ATRX Mouse anti-Human, Clone: 5B3, Invitrogen™

Mouse Monoclonal Antibody

Manufacturer:  Invitrogen MA518469

Catalog No. PIMA518469


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Description

Description

Peptide Sequence: FNLGALSAMS NQQLEDLINQ GREKVVEATN SVTAVRIQPL EDIISAVWKE NMNLSEAQVQ ALALSRQASQ ELDVKRREAI YNDVLTKQQM LISCVQRILM

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.
Specifications

Specifications

ATRX
Monoclonal
0.2-1.0 mg/mL
PBS with no preservative; pH 7.4
P46100
RP5-875J14.1, ATR2, JMS, MRXHF1, RAD54, RAD54L, SFM1, SHS, XH2, XNP, ZNF-HX, ATP-dependent helicase ATRX, DNA dependent ATPase and helicase, RAD54 homolog, X-linked helicase II, X-linked nuclear protein, Zinc finger helicase, alpha thalassemia/mental retardation syndrome X-linked (RAD54 homolog, S. cerevisiae), helicase 2, X-linked, transcriptional regulator ATRX
Mouse
IgG1, kappa
100 μg
-20° C, Avoid Freeze/Thaw Cycles
Primary
546
ELISA, Immunocytochemistry, Immunofluorescence, Western Blot
5B3
Unconjugated
ATRX
Liquid
ATRX
ATRX (NP_000480, 2311 a.a. ∽ 2410 a.a) partial recombit protein with GST tag. MW of the GST tag alone is 26 KDa.
Affinity chromatography
RUO
Antibody
Monoclonal
Human
Documents
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