p53AIP1 Polyclonal Antibody, 20ul PCR Series Mutations in this gene are

Mutations in this gene are associated with an autosomal dominant form of hereditary fibrosing poikiloderma (HFP)

This member is a delayed rectifier potassium channel and its activity is modulated by some other family members

neurotrophins

With 50 rxns and a concentration of 1 rxn/μl

FGFR family members differ from one another in their ligand affinities and tissue distribution

p53AIP1 Polyclonal Antibody, 20ul PCR Series Mutations in this gene areTP53AIP1 (tumor protein p53 regulated apoptosis inducing protein 1) is specifically expressed in the thymus, and encodes a protein that is localized to the mitochondrion. The expression of TP53AIP1 is inducible by p53, and it is thought to play an important role in mediating p53 dependent apoptosis. Alternatively spliced transcript variants encoding different isoforms have been described for TP53AIP1.