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Alomone Labs, LTD
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Reconstitution: 25 µL, 50 µL or 0.2 mL double distilled water (DDW), depending on the sample size. The antibody ships as a lyophilized powder at room temperature. Upon arrival, it should be stored at -20C. The reconstituted solution can be stored at 4C for up to 1 week. For longer periods, small aliquots should be stored at -20C. Avoid multiple freezing and thawing. Centrifuge all antibody preparations before use (10000 x g 5 min).
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 47 type A; connexin 47 type C; connexin 47 type D; Connexin-46.6; Connexin-47; Cx46.6; Cx47; CXG2; Gap junction alpha-12 protein; Gap junction gamma-2 protein; gap junction membrane channel protein alpha 12; gap junction protein, alpha 12; gap junction protein, chi 2; gap junction protein, gamma 2, 47kDa
基因别名: B230382L12Rik; CX46.6; Cx47; GJA12; GJC2; HLD2; LMPH1C; PMLDAR; SPG44
UniProt ID: (Human) Q5T442, (Mouse) Q8BQU6, (Rat) Q80XF7
Entrez Gene ID: (Human) 57165, (Mouse) 118454, (Rat) 497913