GJC2 anticorps

N° du produit ABIN2458256

Détail du produit anti-GJC2 anticorps

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

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp GJC2 est non-conjugé

Application: Western Blotting (WB), ELISA

Purification: Antibody is purified by peptide affinity chromatography method.

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

Information d'application

Indications d'application: 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.

Restrictions: For Research Use only

Stockage

Format: Lyophilized

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

Concentration: 1 mg/mL

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

Conseil sur la manipulation: As with any antibody avoid repeat freeze-thaw cycles.

Stock: 4 °C/-20 °C

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

Détails sur GJC2

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

Autre désignation: GJC2 (GJC2 Produits)

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

Sujet: 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.

Poids moléculaire: 47 kDa

ID gène: 57165

NCBI Accession: NP_065168

UniProt: Q5T442