GJB1 Antilichaam

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.

2705

P08034

Human, Mouse, Rat

Recombinant fusion protein containing a sequence corresponding to amino acids 214-283 of human GJB1 (NP_000157.1) .

Unconjugated

Primary Antibodies

Neuroscience

Affinity purification

LO2

Batch dependent

PBS with 0.02% sodium azide, 50% glycerol, pH7.3.

None

Blue Ice

Store at -20˚ C. Avoid freeze / thaw cycles.

Observed: 32kDa/36kDa

IgG

WB: 1:200 - 1:1000

GJB1

MCF7

293T

A375

Mouse brain

Mouse liver

Gap junction protein, beta 1, 32kDa

Homo sapiens

GJB1, CMTX, CX32, CMTX1

WB

Liquid