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Please note: We are reviewing Western blot images included in the antibody testing data in our catalog, including those provided by third parties. Unless expressly labeled or annotated as “raw-unedited”, Western blot images included in the antibody testing data in our catalog may have been edited, optimized or otherwise adjusted for presentation.
Sequence of this protein is as follows: RLWSLQLILV STPALLVAMH VAHQQHIEKK MLRLEGHGDP LHLEEVKRHK VHISGTLWWT YVISVVFRLL FEAVFMYVFY LLYPGYAMVR LVKCDVYPCP
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-32; GAP junction 28 kDa liver protein; gap junction protein, beta 1, 32kDa; unnamed protein product
基因别名: CMTX; CMTX1; CX32
UniProt ID: (Human) P08034
Entrez Gene ID: (Human) 2705