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Anti-ATRX Rabbit mAb [11G45T02]

Purified Recombinant Rabbit Monoclonal Antibody

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货号 规格 价格
R015841
20µL ¥588.00
50µL ¥1080.00
100µL ¥1780.00

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Anti-ATRX Rabbit mAb [11G45T02]
Anti-ATRX Rabbit mAb [11G45T02]
Product NameAnti-ATRX Rabbit mAb
DescriptionPurified Recombinant Rabbit Monoclonal Antibody
Application
  • Applications Legend:
  • WB=Western Blotting
  • IHC-P=Immunohistochemistry (Paraffin)
  • IHC-F=Immunohistochemistry (Frozen)
  • IP=Immunoprecipitation
  • IF=Immunofluorescence
  • IC=Immunochemistry
  • ICC=Immunocytochemistry
  • FC=Flow Cytometry
  • DB=Dot Blot
WB, IF (Cell)/ICC, ELISA
DilutionWB 1:1,000~1:2,000; IF 1:100~1:200
ReactivityHuman, Mouse, Rat
HostRabbit
ClonalityMonoclonal
Clone No.11G45T02
IsotypeIgG
LabelUnconjugated
ImmunogenRecombinant protein corresponding to the C-terminal of human ATRX
FormatAffinity purified monoclonal antibody supplied in PBS with 0.02% sodium azide and 50% glycerol, pH 7.3.
SynonymsRAD54L; XH2; ATRX; Transcriptional regulator ATRX; ATP-dependent helicase ATRX; X-linked helicase II; X-linked nuclear protein; Znf-HX; XNP.
Molecular weightCalculated MW: 282 kDa; Observed MW: 282 kDa
Uniprot ID P46100
Gene ID 546
StorageShipped on wet ice. Store at -20℃. Stable for 24 months from date of receipt. Aliquoting is unnecessary for -20℃ storage.
PrecautionsAnti-ATRX Rabbit mAb [11G45T02] is for research use only and not for use in diagnostic or therapeutic procedures.
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. 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. Mutations in this gene are associated with X-linked syndromes exhibiting cognitive disabilities as well as 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. Multiple alternatively spliced transcript variants encoding distinct isoforms have been reported. [provided by RefSeq, Jul 2017]
Cellular Location Nucleus.Chromosome.Telomere.Nucleus.PML body.Associated with pericentromeric heterochromatin during interphase and mitosis, probably by interacting with CBX5/HP1 alpha. Colocalizes with histone H3.3, DAXX, HIRA and ASF1A at PML-nuclear bodies. Colocalizes with cohesin (SMC1 and SMC3) and MECP2 at the maternal H19 ICR (By similarity).
Tissue Location Ubiquitous.

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