VCX3 Rabbit Polyclonal Antibody, 50ul Centrifugal Filter and it is known to

and it is known to be a key effector molecule for T-cell- and natural killer-cell-mediated cytolysis

Mutations in this gene have been associated with autosomal mental retardation-39 and autism spectrum disorder

EPHB6 encodes a member of a family of transmembrane proteins that function as receptors for ephrin-B family proteins

retinitis pigmentosa

Unlike the alpha and gamma clusters| the transcripts from these genes are made up of only one large exon| not sharing common 3' exons as expected

VCX3 Rabbit Polyclonal Antibody, 50ul Centrifugal Filter and it is known toThis gene belongs to the VCX Y gene family which has multiple members on both X and Y chromosomes and all are expressed exclusively in male germ cells. The X linked members are clustered on chromosome Xp22 and Y linked members are two identical copies of the gene within a palindromic region on Yq11. The family members share a high degree of sequence identity with the exception that a 30 bp unit is tandemly repeated in X linked members but occurs only