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ATRX Antibody (monoclonal) (M01)

ArtNr ABC-AT1246a
Hersteller Abcepta
Menge 100 ug
Kategorie
Typ Antibody Monoclonal
Format Liquid
Applikationen WB, ELISA
Clon 3C9
Specific against Human (Homo sapiens)
Host Mouse
Isotype IgG1 Kappa
Citations ATRX partners with cohesin and MeCP2 and contributes to developmental silencing of imprinted genes in the brain. Kernohan KD, et al. Dev Cell, 2010 Feb 16. PMID 20159591.Regulation of ICP0-null mutant herpes simplex virus type 1 infection by ND10 components ATRX and hDaxx. Lukashchuk V, et al. J Virol, 2010 Apr. PMID 20147399.ATRX interacts with H3.3 in maintaining telomere structural integrity in pluripotent embryonic stem cells. Wong LH, et al. Genome Res, 2010 Mar. PMID 20110566.Strong relationship between NT-proXNP levels and cardiac output following cardiac surgery in neonates and infants. Breuer T, et al. Acta Anaesthesiol Scand, 2010 Apr. PMID 19919584.Partial ATRX gene duplication causes ATR-X syndrome. Cohn DM, et al. Am J Med Genet A, 2009 Oct. PMID 19764021.
NCBI NP_000480.3,NP_612114.2
ECLASS 10.1 42030590
ECLASS 11.0 42030590
UNSPSC 12352203
Alias Transcriptional regulator ATRX,ATP-dependent helicase ATRX,X-linked helicase II,X-linked nuclear protein,XNP,Znf-HX,ATRX,RAD54L,XH2
Similar products RAD54L, ATRX, XNP, XH2, X-linked nuclear protein, Transcriptional regulator ATRX, ATP-dependent helicase ATRX, X-linked helicase II, Znf-HX
Lieferbar
Manufacturer - Targets
ATRX (NP_000480, 2311 a.a. ~ 2410 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.
Bio 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.
Clonality
Monoclonal
Gene Name
ATRX
Subtitle
Mouse monoclonal antibody raised against a partial recombinant ATRX.
Reactivity
H
Antigen Source
Human: ~~ Positive
Formulation
Clear, colorless solution in phosphate buffered saline, pH 7.2 .
Concentration
1 mg/ml
Dilution
WB: 1:500~1000
E
Org Accession
NP_000480
Gene Description
alpha thalassemia/mental retardation syndrome X-linked (RAD54 homolog, S. cerevisiae)
Gene Summary
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
Antigen Type
Recombinant Protein

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Alle Produkte sind nur für Forschungszwecke bestimmt. Nicht für den menschlichen, tierärztlichen oder therapeutischen Gebrauch.

Menge: 100 ug
Lieferbar: In stock
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