NPC2 Antikörper (AA 20-80)

Produktnummer ABIN1385817

Produktdetails anti-NPC2 Antikörper

Target: NPC2 (Niemann-Pick Disease, Type C2 (NPC2))

Bindungsspezifität: AA 20-80

Reaktivität: Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser NPC2 Antikörper ist unkonjugiert

Applikation: ELISA, Western Blotting (WB)

Kreuzreaktivität: Maus

Homologie: Human,Rat,Cow,Sheep

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human Niemann Pick C2

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB 1:300-5000
ELISA 1:500-1000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 μg/μL

Buffer: 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.

Konservierungsmittel: ProClin

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

Lagerung: 4 °C,-20 °C

Informationen zur Lagerung: Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.

Haltbarkeit: 12 months

Details zu NPC2

Target: NPC2 (Niemann-Pick Disease, Type C2 (NPC2))

Andere Bezeichnung: NPC2/Niemann Pick C2 (NPC2 Produkte)

Synonyme: 2700012J19Rik antikoerper, AA408070 antikoerper, AU045843 antikoerper, HE1 antikoerper, EDDM1 antikoerper, re1 antikoerper, CE1 antikoerper, EPI-1 antikoerper, cb292 antikoerper, sb:cb292 antikoerper, NPC intracellular cholesterol transporter 2 antikoerper, Niemann-Pick disease, type C2 antikoerper, Npc2 antikoerper, NPC2 antikoerper, npc2 antikoerper

Hintergrund:

Synonyms: EDDM1, Epididymal protein 1, Epididymal secretory protein, Epididymal secretory protein E1, HE1, Human epididymis-specic protein 1, Niemann-Pick disease type C2, Niemann-Pick disease type C2 protein, NPC2, NPC2_HUMAN, Tissue specic secretory protein.

Background: NPC2 is a secreted protein mapping against gene 14q24.3 (1,2). NPC2 regulates the lipid composition of sperm membranes during maturation in the epididymis(1,2). Mutations in the NPC2 gene may cause Nieman-Pick type C2 disease and frontal lobe atrophy (1,2,3). Nieman-Pick type C2 is a fatal hereditary disease characterized by defective lysosome release of cholesterol (3). The disease is caused by HE1 deficiency, a lysosmal protein proven to be undetectable in fibroblasts from NPC2 patients (3). This differentiates NPC2 from NPC1, as NPC1 has HE1 protein present (3).

Pathways: SARS-CoV-2 Protein Interaktom