Connexin 47 Polyclonal Antibody

Background:
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.

Research Area: Neuroscience, Signal Transduction

Synonyms:
B230382L12Rik, Connexin 46.6, Connexin 47, Connexin-46.6, Connexin-47, Connexin46.6, Connexin47, CX 46.6, Cx 47, Cx46.6, Cx47, CXG2, Gap junction alpha 12 protein, Gap junction alpha-12 protein, Gap junction gamma 2 protein, Gap junction gamma-2 protein, Gap junction protein alpha 12 47kDa, Gap junction protein gamma 2 47kDa, GAP JUNCTION PROTEIN, 47-KD, gap junction protein, gamma 12, 47kDa, gap junction protein, gamma 2, 47kDa, GJA 12, GJA12, GJC 2, Gjc2, HLD 2, HLD2, LMPH1C, MGC105119, MGC130506, OTTHUMP00000037763, PMLDAR, SPG44

Immunogen: Synthetic peptide of human GJC2

Swissprot: Q5T442
Gene Accession: NP_065168

Purification Method: Affinity purification

Buffer: PBS with 0.05% sodium azide and 50% glycerol, PH7.4

Concentration: 0.5 mg/mL
Dilution: IHC 1:50-1:200

Storage:
Store at -20°C. Avoid freeze / thaw cycles.