Nyctalopin Antikörper (N-Term)

Produktnummer ABIN953798

Produktdetails anti-Nyctalopin Antikörper

Target: Nyctalopin (NYX)

Bindungsspezifität: AA 59-89, N-Term

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser Nyctalopin Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), Enzyme Immunoassay (EIA)

Spezifität: This antibody recognizes Human Nyctalopin (N-term).

Aufreinigung: Protein A column, followed by peptide affinity purification

Immunogen: KLH conjugated synthetic peptide between 59~89 amino acids from the N-terminal region of Human Nyctalopin. Genename: NYX

Isotyp: Ig Fraction

Anwendungsinformationen

Applikationshinweise: Optimal working dilution should be determined by the investigator.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 0.25 mg/mL

Buffer: PBS containing 0.09 % (W/V) Sodium Azide as preservative

Konservierungsmittel: Sodium azide

Vorsichtsmaßnahmen: This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Handhabung: Avoid repeated freezing and thawing.

Lagerung: 4 °C/-20 °C

Informationen zur Lagerung: Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.

Details zu Nyctalopin

Target: Nyctalopin (NYX)

Andere Bezeichnung: Nyctalopin (NYX Produkte)

Synonyme: MGC84276 antikoerper, CLRP antikoerper, CSNB1 antikoerper, CSNB1A antikoerper, CSNB4 antikoerper, NBM1 antikoerper, CLNP antikoerper, nob antikoerper, RGD1561300 antikoerper, nyctalopin antikoerper, nyctalopin L homeolog antikoerper, uncharacterized LOC491837 antikoerper, NYX antikoerper, nyx.L antikoerper, LOC491837 antikoerper, nyx antikoerper, Nyx antikoerper

Hintergrund: 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].Synonyms: CLRP, NYX

Molekulargewicht: 52000 Da

Gen-ID: 60506

NCBI Accession: NP_072089