HXC13 Polyclonal Antibody, 50ul Protein Expression Mutations in this gene cause

Mutations in this gene cause startle disease

This gene encodes a member of the S100 protein family which contains an EF-hand motif and binds calcium

protein kinases CDC2 and CDC7

The CD24 molecule is cleaved to a short 32 amino acid mature peptide which is anchored via a glycosyl phosphatidylinositol (GPI) link to the cell surface

HXC13 Polyclonal Antibody, 50ul Protein Expression Mutations in this gene causeThis gene belongs to the homeobox family of genes. The homeobox genes encode a highly conserved family of transcription factors that play an important role in morphogenesis in all multicellular organisms. Mammals possess four similar homeobox gene clusters, HOXA, HOXB, HOXC and HOXD, which are located on different chromosomes and consist of 9 to 11 genes arranged in tandem. This gene is one of several homeobox HOXC genes located in a cluster on