ATRX antibody [39f]

Cannot supply to this region.

SKU:: GTX34418
Additional Names:: ATR2 , ATRX , ATRX, chromatin remodeler , JMS , MRX52 , MRXHF1 , RAD54 , RAD54L , SFM1 , SHS , XH2 , XNP , ZNFHX , ATRX chromatin remodeler
Application:: IHC-P
Concentration:: 0.2 mg/ml
Physical State:: Liquid
Species Reactivity:: Human
Purification:: protein a/g purified
Storage Conditions:: -20[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., 2-8[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., -20[o]C/-70[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted.
Supplier:: Genetex
Host:: Mouse
Reactivities:: Human
Buffer:: PBS, 0.05% BSA, 0.05% Sodium azide.
Immunogen:: Recombinant full-length human ATRX protein
Clone:: 39f
Uniprot:: P46100
Synonyms:: alpha thalassemia/mental retardation syndrome X-linked (RAD54 homolog, S. cerevisiae);ATP-dependent helicase ATRX;JMS;MRX52;RAD54;RAD54L;transcriptional regulator ATRX;X-linked helicase II;X-linked nuclear protein;XH2;XNP;ZNF-HX
Extra Details:: 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]

Shipping Conditions:: Blue Ice