Recombinant fusion protein of human ZMYM3(NP_001164634.1).
Conjugation:
Unconjugated
Alternative Names:
ZMYM3,DXS6673E,MYM,XFIM,ZNF198L2,ZNF261
This gene is located on the X chromosome and is subject to X inactivation. It is highly conserved in vertebrates and most abundantly expressed in the brain. The encoded protein is a component of histone deacetylase-containing multiprotein complexes that function through modifying chromatin structure to keep genes silent. A chromosomal translocation (X,13) involving this gene is associated with X-linked mental retardation. Several alternatively spliced transcript variants have been found for this gene.
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE).
Form:
1mg/ml in PBS with 0.02% sodium azide, 50% glycerol, pH7.2
Application Dilute:
WB,1:500 - 1:2000|IHC,1:50 - 1:200
Application Notes:
Unmodification
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