NPBW1 Polyclonal Antibody, 20ul Pipette Holder A mutation in this gene

A mutation in this gene has been associated with selective 25-hydroxyvitamin D deficiency

and a tyrosine kinase (TK) domain within the cytoplasmic domain

POU class 2 homeobox 2 binds the octamer sequence 5'-ATTTGCAT-3'

RCC1 (regulator of chromatin condensation 1) is the only known RanGEF

This gene encodes a coiled-coil domain-containing protein

NPBW1 Polyclonal Antibody, 20ul Pipette Holder A mutation in this geneInteracts specifically with a number of opioid ligands. Receptor for neuropeptides B and W, which may be involved in neuroendocrine system regulation, food intake and the organization of other signals. Has a higher affinity for neuropeptide B.,Belongs to the G protein coupled receptor 1 family.,tissue specificity: Found in cerebellum and frontal cortex. Detected at high levels in hipppocampus, amygdala and trachea; at moderate levels in fetal brain,