Nyctalopin Antikörper
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- Target Alle Nyctalopin (NYX) Antikörper anzeigen
- Nyctalopin (NYX)
- Reaktivität
- Human, Maus
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser Nyctalopin Antikörper ist unkonjugiert
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Applikation
- Immunohistochemistry (IHC)
- Produktmerkmale
- Polyclonal Antibody
- Aufreinigung
- Affinity purification
- Immunogen
- Recombinant fusion protein of human NYX (NP_072089.1).
- Isotyp
- IgG
- Top Product
- Discover our top product NYX Primärantikörper
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anti-Nyctalopin (NYX) (AA 282-481) antibody
NYX Reaktivität: Human WB, IHC, ELISA Wirt: Kaninchen Polyclonal unconjugated
anti-Nyctalopin (NYX) (AA 53-80), (N-Term) antibodyNYX Reaktivität: Human WB Wirt: Kaninchen Polyclonal RB23621 unconjugated
anti-Nyctalopin (NYX) (AA 59-89), (N-Term) antibodyNYX Reaktivität: Human WB, EIA Wirt: Kaninchen Polyclonal unconjugated
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- Applikationshinweise
- IHC 1:50-1:100
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Konzentration
- 1 mg/mL
- 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.
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- 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.
- Gen-ID
- 60506
- UniProt
- Q9GZU5
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