MUC7 Polyclonal Antibody, 20ul Cryopreservation Mutations in PMS1 cause hereditary

Mutations in PMS1 cause hereditary nonpolyposis colorectal cancer type 3 (HNPCC3) either alone or in combination with mutations in other genes involved in the HNPCC phenotype

which is known as a precursor of the cornified cell envelope

CCZ1B or CGI-43

including regulation of iron homeostasis

This kinase itself can be phosphorylated and activated by MAP3K3/MEKK3

MUC7 Polyclonal Antibody, 20ul Cryopreservation Mutations in PMS1 cause hereditaryThis gene encodes a small salivary mucin, which is thought to play a role in facilitating the clearance of bacteria in the oral cavity and to aid in mastication, speech, and swallowing. The central domain of this glycoprotein contains tandem repeats, each composed of 23 amino acids. This antimicrobial protein has antibacterial and antifungal activity. The most common allele contains 6 repeats, and some alleles may be associated with susceptibility to