MYO7A Polyclonal Antibody (E-AB-13433)
For research use only.
| Verified Samples |
Verified Samples in IHC: Human thyroid cancer, Human brain |
| Dilution | IHC 1:25-1:100 |
| Isotype | IgG |
| Host | Rabbit |
| Reactivity | Human, Mouse |
| Applications | IHC |
| Clonality | Polyclonal |
| Immunogen | Synthetic peptide of human MYO7A |
| Abbre | MYO7A |
| Synonyms | DFNA11, DFNB 2, DFNB2, Deafness autosomal dominant 11, Deafness autosomal recessive 2, MYOVIIA, MYU7A, Myo7a, Myosin, Myosin 7a, Myosin VIIA (Usher syndrome 1B (autosomal recessive, Myosin VIIa, NSRD 2, NSRD2, Unconventional , family VII, member A, severe)), unconventional |
| Swissprot | |
| Cellular Localization | Cytoplasmic, cytoskeleton. |
| Concentration | 0.5 mg/mL |
| Buffer | Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol. |
| Purification Method | Affinity purification |
| Research Areas | Cancer, Signal Transduction |
| Conjugation | Unconjugated |
| Storage | Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles. |
| Shipping | The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended. |
| background | 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. |
Other Clones
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Other Formats
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Unconjugated
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