NYX Polyclonal Antibody | G-AB-11889

NYX Polyclonal Antibody | G-AB-11889 | Gentaur Antibodies

Overview: 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.

Category Type: Polyclonal Antibody

Research Areas:

Synonyms: NYX, CLRP, CSNB1, CSNB1A, CSNB4, NBM1

Reactivity: Human, Mouse

Host: Rabbit

Isotype: IgG

Gene ID: 60506

Accession #:

Clonality:

Immunogen: Recombinant fusion protein of human NYX (NP_072089.1) .

Clone #:

Conjugation: Unconjugated

Swissprot: Q9GZU5

Santa Cruz:

Calculated MW:

Observed MW:

Concentration: 1 mg/mL

Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3

Purification method: Affinity purification

Application: IHC

Dilution: IHC 1:50-1:100

Storage: Store at -20°C. Avoid freeze / thaw cycles.

NYX Polyclonal Antibody DataSheet