NPC2 Rekombinanter Antikörper

NPC2 Rekombinant Antikörper für WB, IF/ICC, ELISA

Wirt / Isotyp

Kaninchen / IgG

Getestete Reaktivität

human, Maus

Anwendung

WB, IF/ICC, ELISA

Konjugation

Unkonjugiert

CloneNo.

250911E11

Kat-Nr. : 86293-1-RR

Synonyme

He1, Human epididymis-specific protein 1, Niemann-Pick disease type C2 protein



Geprüfte Anwendungen

Erfolgreiche Detektion in WBA549-Zellen, HepG2-Zellen, HT-1080.Zellen, Mausnierengewebe, Mauslungengewebe
Erfolgreiche Detektion in IF/ICCHeLa-Zellen

Empfohlene Verdünnung

AnwendungVerdünnung
Western Blot (WB)WB : 1:5000-1:50000
Immunfluoreszenz (IF)/ICCIF/ICC : 1:250-1:1000
It is recommended that this reagent should be titrated in each testing system to obtain optimal results.
Sample-dependent, check data in validation data gallery

Produktinformation

86293-1-RR bindet in WB, IF/ICC, ELISA NPC2 und zeigt Reaktivität mit human, Maus

Getestete Reaktivität human, Maus
Wirt / Isotyp Kaninchen / IgG
Klonalität Rekombinant
Typ Antikörper
Immunogen NPC2 fusion protein Ag13719
Vollständiger Name Niemann-Pick disease, type C2
Berechnetes Molekulargewicht 151 aa, 17 kDa
Beobachtetes Molekulargewicht17-21 kDa
GenBank-ZugangsnummerBC002532
Gene symbol NPC2
Gene ID (NCBI) 10577
Konjugation Unkonjugiert
Form Liquid
Reinigungsmethode Protein-A-Reinigung
Lagerungspuffer PBS with 0.02% sodium azide and 50% glycerol
LagerungsbedingungenBei -20°C lagern. Nach dem Versand ein Jahr lang stabil Aliquotieren ist bei -20oC Lagerung nicht notwendig. 20ul Größen enthalten 0,1% BSA.

Hintergrundinformationen

Niemann-Pick Type C (NPC) disease is a lysosomal storage disorder characterized by accumulation of unesterified cholesterol and other lipids in the endolysosomal system. NPC disease results from a defect in either of two distinct cholesterol-binding proteins: a transmembrane protein, NPC1, and a small soluble protein, NPC2. NPC1 or NPC2 deficiency models showed that the function of these two proteins within lysosomes are linked closely. NPC2 is also named human epididymis-specific protein 1 (HE1), defects of which are the cause of Niemann-Pick disease type C2, characterized as a lysosomal storage disorder that affects the viscera and the central nervous system. Recent finding suggests that NPC2 may serve as a novel intracrine/autocrine factor that controls adipocyte differentiation and function as well as potential therapeutic target for the treatment of type 2 diabetes and related metabolic disorders.

Protokolle

PRODUKTSPEZIFISCHE PROTOKOLLE
WB protocol for NPC2 antibody 86293-1-RRProtokoll herunterladen
IF protocol for NPC2 antibody 86293-1-RRProtokoll herunterladen
STANDARD-PROTOKOLLE
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