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34-4200 was used in the IHC analysis to successfully detect Connexin 29 in mouse sciatic nerve.
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.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: connexin 29; Connexin-29; Connexin-30.2; Connexin-31.3; Cx29; Cx30.2; Cx31.3; Gap junction epsilon-1 protein; Gap junction gamma-3 protein; gap junction membrane channel protein epsilon 1; gap junction protein, gamma 3, 30.2kDa
基因别名: CX29; CX30.2; CX31.3; GJC3; GJE1
UniProt ID: (Human) Q8NFK1, (Mouse) Q921C1
Entrez Gene ID: (Human) 349149, (Mouse) 118446