VCX3B 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 family members share a high degree of sequence identity, with the exception that a 30-nt unit is tandemly repeated in X-linked members but occurs only once in Y-linked members. The VCX gene cluster is polymorphic in terms of copy number; different individuals may have a different number of VCX genes. This family member, as represented by the reference genome allele, contains 14 copies of the 30-nt repeat unit. VCX/Y genes encode small and highly charged proteins containing putative bipartite nuclear localization signals. Although the exact function of this family member has yet to be determined, a role in mRNA stability regulation can be inferred from the ability of the highly similar family member, VCX-A, to inhibit mRNA decapping.
Organism species: Homo sapiens (Human)
CATALOG NO. | PRODUCT NAME | APPLICATIONS | |
Proteins | n/a | Recombinant Variable Charge, X-Linked 3B (VCX3B) | Recombinant Protein Customized Service Offer |
Antibodies | n/a | Monoclonal Antibody to Variable Charge, X-Linked 3B (VCX3B) | Monoclonal Antibody Customized Service Offer |
n/a | Polyclonal Antibody to Variable Charge, X-Linked 3B (VCX3B) | Polyclonal Antibody Customized Service Offer | |
Assay Kits | n/a | CLIA Kit for Variable Charge, X-Linked 3B (VCX3B) | CLIA Kit Customized Service Offer |
n/a | ELISA Kit for Variable Charge, X-Linked 3B (VCX3B) | ELISA Kit Customized Service Offer |
- "The DNA sequence of the human X chromosome." Nature 434:325-337(2005) [PubMed] [Europe PMC] [Abstract]
- "A member of a gene family on Xp22.3, VCX-A, is deleted in patients with X-linked nonspecific mental retardation."Am. J. Hum. Genet. 67:563-573(2000) [PubMed] [Europe PMC] [Abstract]
- "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."Genome Res. 14:2121-2127(2004) [PubMed] [Europe PMC] [Abstract]