NYX Antibody (N-term)

Synthetic Peptide

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. [provided by RefSeq].

Polyclonal

60506

Affinity Purified Rabbit Polyclonal Antibody (Pab)

Western blot analysis of NYX Antibody (N-term) (Cat. #AP9483a) in HL-60 cell line lysates (35ug/lane). NYX (arrow) was detected using the purified Pab.

1:1000

Rabbit Ig

53-80

This NYX antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 53-80 amino acids from the N-terminal region of human NYX.