PCNT Polyclonal Antibody, 20ul Glassware Mutations in this gene lead

Mutations in this gene lead to Jackson-Lawler type pachyonychia congenita and steatocystoma multiplex

it is involved in the inhibition of neutrophil degranulation in neutrophil-mediated tissue injury

and a corresponding pseudogene has been found on chromosome 22

allowing for endless possibilities in your experiments

This syndrome is characterized by a profuse sweating after exposure to cold as well as congenital physical abnormalities of the head and spine

PCNT Polyclonal Antibody, 20ul Glassware Mutations in this gene leadThe protein encoded by this gene binds to calmodulin and is expressed in the centrosome. It is an integral component of the pericentriolar material (PCM). The protein contains a series of coiled coil domains and a highly conserved PCM targeting motif called the PACT domain near its C terminus. The protein interacts with the microtubule nucleation component gamma tubulin and is likely important to normal functioning of the centrosomes, cytoskeleton,