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Description
This gene is a member of the myosin gene family. Myosins are mechanochemical proteins characterized by the presence of a motor domain, an actin-binding domain, a neck domain that interacts with other proteins, and a tail domain that serves as an anchor. This gene encodes an unconventional myosin with a very short tail. Defects in this gene are associated with the mouse shaker-1 phenotype and the human Usher syndrome 1B which are characterized by deafness, reduced vestibular function, and (in human) retinal degeneration. Alternative splicing results in multiple transcript variants. [provided by RefSeq
Specifications
Specifications
| Antigen | MYO7A |
| Applications | ELISA, Western Blot |
| Classification | Polyclonal |
| Conjugate | Unconjugated |
| Description | Mouse polyclonal antibody raised against a partial recombinant MYO7A. |
| Formulation | 50% glycerol |
| Gene | MYO7A |
| Gene Accession No. | NM_000260 |
| Gene Alias | DFNA11/DFNB2/MYOVIIA/MYU7A/NSRD2/USH1B |
| Gene Symbols | MYO7A |
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