AR-Beta3 Polyclonal Antibody, 50ul Isothermal Amplification Defects in PPT1 are a

Defects in PPT1 are a cause of infantile neuronal ceroid lipofuscinosis 1 (CLN1

This gene is one member of a family of alpha-spectrin genes

This gene has been shown to repress lamellipodial extension and focal adhesion turnover| and is thought to regulate cell motility

helping you achieve your boldest research goals

The protein encoded by this gene belongs to the HIN-200 family of interferon-inducible proteins that share a 200-amino acid signature motif at their C-termini

AR-Beta3 Polyclonal Antibody, 50ul Isothermal Amplification Defects in PPT1 are aBeta 3 adrenergic receptor encoded by ADRB3 belongs to the family of beta adrenergic receptors, which mediate catecholamine induced activation of adenylate cyclase through the action of G proteins. This receptor is located mainly in the adipose tissue and is involved in the regulation of lipolysis and thermogenesis.