NMNA3 Rabbit Polyclonal Antibody, 50ul Plasma and mutations in this gene

and mutations in this gene are a cause of hereditary leukonychia

May fulfill a function related to the motile behaviors of developing neurons

DGC forms a link between the F-actin cytoskeleton and the extracellular matrix

Retinoic acid plays a critical role in development

It is an atypical calpain in that it lacks the calmodulin-like calcium-binding domain and instead has a divergent C-terminal domain

NMNA3 Rabbit Polyclonal Antibody, 50ul Plasma and mutations in this geneThis gene encodes a member of the nicotinamide nicotinic acid mononucleotide adenylyltransferase family. These enzymes use ATP to catalyze the synthesis of nicotinamide adenine dinucleotide or nicotinic acid adenine dinucleotide from nicotinamide mononucleotide or nicotinic acid mononucleotide respectively. The encoded protein is localized to mitochondria and may also play a neuroprotective role as a molecular chaperone. Alternatively spliced