Nyctalopin Antikörper (AA 282-481)

Produktnummer ABIN6144979

Produktdetails anti-Nyctalopin Antikörper

Target: Nyctalopin (NYX)

Bindungsspezifität: AA 282-481

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser Nyctalopin Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), Immunohistochemistry (IHC)

Sequenz: LLYLDRNSIA FVEEGAFQNL SGLLALHLNG NRLTVLAWVA FQPGFFLGRL FLFRNPWCCD CRLEWLRDWM EGSGRVTDVP CASPGSVAGL DLSQVTFGRS SDGLCVDPEE LNLTTSSPGP SPEPAATTVS RFSSLLSKLL APRVPVEEAA NTTGGLANAS LSDSLSSRGV GGAGRQPWFL LASCLLPSVA QHVVFGLQMD

Kreuzreaktivität: Human, Maus

Produktmerkmale: Polyclonal Antibodies

Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 282-481 of human NYX (NP_072089.1).

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB,1:500 - 1:2000,IHC,1:50 - 1:100

Kommentare:

HIGH QUALITY

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

Konservierungsmittel: Sodium azide

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

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20°C. Avoid freeze / thaw cycles.

Details zu Nyctalopin

Target: Nyctalopin (NYX)

Andere Bezeichnung: NYX (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.,NYX,CLRP,CSNB1,CSNB1A,CSNB4,NBM1,Neuroscience,NYX

Molekulargewicht: 52 kDa

Gen-ID: 60506

UniProt: Q9GZU5