GJC2 Antikörper

Produktnummer ABIN2458256

Produktdetails anti-GJC2 Antikörper

Target: GJC2 (Gap Junction Protein, gamma 2, 47kDa (GJC2))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser GJC2 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), ELISA

Aufreinigung: Antibody is purified by peptide affinity chromatography method.

Immunogen: Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human GJC2.

Anwendungsinformationen

Applikationshinweise: GJC2 antibody can be used for detection of GJC2 by ELISA at 1:312500. GJC2 antibody can be used for detection of GJC2 by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Lyophilized

Rekonstitution: Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.

Konzentration: 1 mg/mL

Buffer: Antibody is lyophilized in PBS buffer with 2 % sucrose.

Handhabung: As with any antibody avoid repeat freeze-thaw cycles.

Lagerung: 4 °C/-20 °C

Informationen zur Lagerung: For short periods of storage (days) store at 4 °C. For longer periods of storage, store GJC2 antibody at -20 °C.

Details zu GJC2

Target: GJC2 (Gap Junction Protein, gamma 2, 47kDa (GJC2))

Andere Bezeichnung: GJC2 (GJC2 Produkte)

Synonyme: GJA12 antikoerper, cx47 antikoerper, gja12 antikoerper, cx46.6 antikoerper, pmldar antikoerper, MGC146420 antikoerper, B230382L12Rik antikoerper, Cx47 antikoerper, Gja12 antikoerper, CX46.6 antikoerper, HLD2 antikoerper, LMPH1C antikoerper, PMLDAR antikoerper, SPG44 antikoerper, gap junction protein gamma 2 antikoerper, si:dkey-91f15.1 antikoerper, gap junction protein, gamma 2 antikoerper, GJC2 antikoerper, gjc2 antikoerper, si:dkey-91f15.1 antikoerper, Gjc2 antikoerper

Hintergrund: GJC2 is a gap junction protein. Gap junction proteins are members of a large family of homologous connexins and comprise 4 transmembrane, 2 extracellular, and 3 cytoplasmic domains. This gene plays a key role in central myelination and is involved in peripheral myelination in humans. Defects in this gene are the cause of autosomal recessive Pelizaeus-Merzbacher-like disease-1.This gene encodes a gap junction protein. Gap junction proteins are members of a large family of homologous connexins and comprise 4 transmembrane, 2 extracellular, and 3 cytoplasmic domains. This gene plays a key role in central myelination and is involved in peripheral myelination in humans. Defects in this gene are the cause of autosomal recessive Pelizaeus-Merzbacher-like disease-1.

Molekulargewicht: 47 kDa

Gen-ID: 57165

NCBI Accession: NP_065168

UniProt: Q5T442