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

Mutations in KAL1 cause the X-linked Kallmann syndrome

TMEM55A catalyzes the degradation of phosphatidylinositol 4|5-bisphosphate (PtdIns-4|5-P2) by removing the 4-phosphate (Ungewickell et al

This gene is also involved in several chromosomal translocations that are associated with lymphoid malignancies including pre-B-cell acute lymphoblastic leukemia (t(1|19)

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

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