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>   首页   >   KD-Validated Anti-SMCHD1 Rabbit Monoclonal Antibody   

KD-Validated Anti-SMCHD1 Rabbit Monoclonal Antibody

Rabbit monoclonal antibody

     
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Product Information
Application
  • Applications Legend:
  • E=ELISA
  • WB=Western Blotting
  • IHC=Immunohistochemistry
  • IHC-P=Immunohistochemistry (Paraffin)
  • IP=Immunoprecipitation
  • IF=Immunofluorescence
  • IC=Immunochemistry
  • ICC=Immunocytochemistry
  • FC=Flow Cytometry
  • DB=Dot Blot
WB, ICC
Primary Accession A6NHR9
Reactivity Rat, Human
Clonality Monoclonal
Isotype Rabbit IgG
Clone Names 24GB2385
Calculated MW 226374 Da
Gene Name SMCHD1
Aliases SMCHD1; Structural Maintenance Of Chromosomes Flexible Hinge Domain Containing 1; KIAA0650; FSHD2; Structural Maintenance Of Chromosomes Flexible Hinge Domain-Containing Protein 1; SMC Hinge Domain-Containing Protein 1; EC 3.6.1.-; BAMS
Immunogen A synthesized peptide derived from human SMCHD1
Additional Information
Gene ID 23347
Other Names Structural maintenance of chromosomes flexible hinge domain-containing protein 1, 3.6.1.-, SMCHD1 (HGNC:29090)

For Research Use Only. Not For Use In Diagnostic Procedures.

Protein Information
Name SMCHD1 (HGNC:29090)
Function Non-canonical member of the structural maintenance of chromosomes (SMC) protein family that plays a key role in epigenetic silencing by regulating chromatin architecture (By similarity). Promotes heterochromatin formation in both autosomes and chromosome X, probably by mediating the merge of chromatin compartments (By similarity). Plays a key role in chromosome X inactivation in females by promoting the spreading of heterochromatin (PubMed:23542155). Recruited to inactivated chromosome X by Xist RNA and acts by mediating the merge of chromatin compartments: promotes random chromatin interactions that span the boundaries of existing structures, leading to create a compartment-less architecture typical of inactivated chromosome X (By similarity). Required to facilitate Xist RNA spreading (By similarity). Also required for silencing of a subset of clustered autosomal loci in somatic cells, such as the DUX4 locus (PubMed:23143600). Has ATPase activity; may participate in structural manipulation of chromatin in an ATP-dependent manner as part of its role in gene expression regulation (PubMed:29748383). Also plays a role in DNA repair: localizes to sites of DNA double-strand breaks in response to DNA damage to promote the repair of DNA double-strand breaks (PubMed:24790221, PubMed:25294876). Acts by promoting non- homologous end joining (NHEJ) and inhibiting homologous recombination (HR) repair (PubMed:25294876).
Cellular Location Chromosome. Note=Recruited to inactivated chromosome X in females by Xist RNA (By similarity). Localizes at sites of DNA damage at double-strand breaks (DSBs) (PubMed:24790221, PubMed:25294876). {ECO:0000250|UniProtKB:Q6P5D8, ECO:0000269|PubMed:24790221, ECO:0000269|PubMed:25294876}
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