NPBW1 Polyclonal Antibody, 50ul Cell Culture & Maintenance The lack of RFX binding

The lack of RFX binding activity in complementation group C results from mutations in the RFX5 gene encoding the 75-kD subunit of RFX (Steimle et al

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This gene is located in a chromosomal region that was genetically linked to Parkinson disease type 11

induction:By MYC overexpression in a concentration dependent manner in neuroblastoma cell line

NPBW1 Polyclonal Antibody, 50ul Cell Culture & Maintenance The lack of RFX bindingInteracts 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,