KLK13 Polyclonal Antibody, 20ul Cell Function Analysis Various mutations of PMP22 are

Various mutations of PMP22 are causes of Charcot-Marie-Tooth disease Type IA

and library packaging

This protein was demonstrated to interact with and inhibit the activities of both C alpha and C beta catalytic subunits of the PKA

However| other mechanisms are also thought to be involved| as anti-viral effect is not dependent on deaminase activity

NK2 homeobox 1

KLK13 Polyclonal Antibody, 20ul Cell Function Analysis Various mutations of PMP22 areKallikreins are a subgroup of serine proteases having diverse physiological functions. Growing evidence suggests that many kallikreins are implicated in carcinogenesis and some have potential as novel cancer and other disease biomarkers. This gene is one of the fifteen kallikrein subfamily members located in a cluster on chromosome 19. Expression of this gene is regulated by steroid hormones and may be useful as a marker for breast cancer. An