NYX

BT-AP03898

Rabbit

IgG

100ul,50ul,20ul

Polyclonal

Synthesized peptide derived from human NYX

The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen.

1 mg/ml

Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.

-20°C for 1 year

The product of this gene belongs to the small leucine-rich proteoglycan (SLRP) family of proteins. Defects in this gene are the cause of congenital stationary night blindness type 1 (CSNB1)| also called X-linked congenital stationary night blindness (XLCSNB). CSNB1 is a rare inherited retinal disorder characterized by impaired scotopic vision| myopia| hyperopia| nystagmus and reduced visual acuity. The role of other SLRP proteins suggests that mutations in this gene disrupt developing retinal interconnections involving the ON-bipolar cells| leading to the visual losses seen in patients with complete CSNB.

Human: Q9GZU5; Mouse: P83503;

52910

Human: 60506; Mouse: 236690

NYX

Neuroscience

NYX