HP1 alpha(Phospho Ser92) Polyclonal Antibody, 100ul Cryopreservation Mutations in KAL1 cause the

Mutations in KAL1 cause the X-linked Kallmann syndrome

This member also belongs to the F-box protein family which is characterized by an approximately 40 amino acid motif

where it maintains nucleolar structure and cell growth rates

The acrosomal vesicle protein 1 may be involved in sperm-zona binding or penetration

Contains 2 Link domains

HP1 alpha(Phospho Ser92) Polyclonal Antibody, 100ul Cryopreservation Mutations in KAL1 cause theThis gene encodes a highly conserved nonhistone protein, which is a member of the heterochromatin protein family. The protein is enriched in the heterochromatin and associated with centromeres. The protein has a single N terminal chromodomain which can bind to histone proteins via methylated lysine residues, and a C terminal chromo shadow domain (CSD) which is responsible for the homodimerization and interaction with a number of chromatin associated