PTN9 Polyclonal Antibody, 20ul PCR Series Mutations in this gene cause

Mutations in this gene cause autosomal-dominant polycystic kidney and liver disease

Calcineurin B homologous protein 1 serves as an essential cofactor which supports the physiological activity of NHE family members and may play a role in the mitogenic regulation of NHE1

The CCR4-NOT complex plays a role in many cellular processes| including miRNA-mediated repression| mRNA degradation| and transcriptional regulation

This gene encodes a member of the SLC26 gene family of anion transporters

PTN9 Polyclonal Antibody, 20ul PCR Series Mutations in this gene causeThe protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation. This PTP contains an N terminal domain that shares a significant similarity with yeast SEC14, which is a protein that has phosphatidylinositol transfer activity and is required for protein