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Description
This gene is a member of the connexin gene family. The encoded protein is a component of gap junctions, which are composed of arrays of intercellular channels that provide a route for the diffusion of low molecular weight materials from cell to cell. Mutations in this gene can cause nonsyndromic deafness or erythrokeratodermia variabilis, a skin disorder. Alternative splicing results in multiple transcript variants encoding the same protein. [provided by RefSeq
Specifications
Specifications
| Antigen | GJB3 |
| Applications | ELISA, Immunofluorescence, Western Blot |
| Classification | Monoclonal |
| Clone | 3B4-1B3 |
| Conjugate | Unconjugated |
| Description | Mouse monoclonal antibody raised against a full length recombinant GJB3. |
| Formulation | PBS with no preservative; pH 7.4 |
| Gene | GJB3 |
| Gene Accession No. | BC012918 |
| Gene Alias | CX31/DFNA2/EKV/FLJ22486/MGC102938 |
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