MYO7A Polyclonal Antibody (E-AB-16626)

For research use only.
Verified Samples |
Verified Samples in IHC: Human prostate cancer, Human brain |
Dilution | IHC 1:50-1:200 |
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 | 0.6 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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