Background:

This gene encodes a member of the gap junction protein family. The gap junction proteins are membrane-spanning proteins that assemble to form gap junction channels that facilitate the transfer of ions and small molecules between cells. According to sequence similarities at the nucleotide and amino acid levels, the gap junction proteins are divided into two categories, alpha and beta. Mutations in this gene cause X-linked Charcot-Marie-Tooth disease, an inherited peripheral neuropathy. Alternatively spliced transcript variants encoding the same protein have been found for this gene.

Specificity:

Connexin 32 polyclonal antibody detects endogenous levels of Connexin 32 protein.

Alternative names:

Cx32, GJB1, CX32, Charcot Marie Tooth neuropathy X linked, CMTX 1, CMTX, CMTX1, Connexin-32, Connexin32, CX 32, Cx32, CXB1, GAP junction 28 kDa liver protein, Gap junction beta 1 protein, Gap junction beta-1 protein, Gap junction protein beta 1 32kD, Gap junction protein beta 1, GJB 1, GJB1,

Species reactivity:

Human,Mouse

Host:

Rabbit

Ig type:

Rabbit IgG, 1mg/ml in PBS with 0.02% sodium azide, 50% glycerol, pH7.2

Immunogen:

Synthetic peptide within mouse Connexin-32 aa 230-265.

Purification & Purity:

Peptide affinity purified.

Molecular weight:

32 kDa

Applications:

WB FC

Usage:

WB:1:500 FC:1:50-1:100

Storage:

Store at +4°C after thawing. Aliquot store at -20°C. Avoid repeated freeze / thaw cycles.

Precautions:

For research use only, not for use in diagnostic procedure.

More info:

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