GJC2 Antikörper (N-Term)

Produktnummer ABIN1538737

Produktdetails anti-GJC2 Antikörper

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

Bindungsspezifität: AA 32-61, N-Term

Reaktivität: Human

Wirt: Maus

Klonalität: Monoklonal

Konjugat: Dieser GJC2 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Aufreinigung: This antibody is prepared by Euglobin precipitation followed by dialysis against PBS.

Immunogen: This GJC2 antibody is generated from mice immunized with a KLH conjugated synthetic peptide between 32-61 amino acids from the N-terminal region of human GJC2.

Klon: 391CT6-4-3

Isotyp: IgM

Anwendungsinformationen

Applikationshinweise: WB: 1:100~500

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: Purified monoclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

Konservierungsmittel: Sodium azide

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

Lagerung: 4 °C,-20 °C

Informationen zur Lagerung: GJC2 Antibody (N-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

Haltbarkeit: 6 months

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.

Molekulargewicht: 47002

Gen-ID: 57165

NCBI Accession: NP_065168

UniProt: Q5T442