HAND1 Monoclonal Antibody, 100ul Pipette Filler were originally characterized based on

were originally characterized based on their interaction with the Stat family of transcription factors

other named neuronal pentraxin receptor (NPR)

Mutations in this gene may result in Netherton syndrome

and Zellweger syndrome

Involved in autophagy in controlling protein turnover during neuronal development

HAND1 Monoclonal Antibody, 100ul Pipette Filler were originally characterized based onThe protein encoded by this gene belongs to the basic helix loop helix family of transcription factors. This gene product is one of two closely related family members, the HAND proteins, which are asymmetrically expressed in the developing ventricular chambers and play an essential role in cardiac morphogenesis. Working in a complementary fashion, they function in the formation of the right ventricle and aortic arch arteries, implicating them as