MYO7A rabbit pAb
Ref. EK-ES9855
| 50µl | 188.00 € | ||
| 100µl | 316.00 € |
Product Information
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, Jul 2008],
Chemical properties
Technical inquiry about: EK-ES9855 MYO7A rabbit pAb
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