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SKU: E-AB-16626_60μL-ES
MYO7A Polyclonal Antibody, 60 μL
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.
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Product Specification
Basic Information
Brands:Elabscience
Model Number:
Place of Origin:China
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Shipping:The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended.
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Concentration:0.6 mg/mL
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Shelf Life:12 months
Storage:Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.
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Dilution:IHC 1:50-1:200
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Application:IHC
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Research Areas:Cancer;Signal transduction
Species Reactivity:Human;Mouse
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Target Synonym:Deafness autosomal dominant 11;Deafness autosomal recessive 2;DFNA11;DFNB 2;DFNB2;Myo7a;Myosin 7a;Myosin VIIA (Usher syndrome 1B (autosomal recessive;severe));Myosin VIIa;Myosin;unconventional;family VII;member A;MYOVIIA;MYU7A;NSRD 2;NSRD2;Unconventional myosin VIIa;Ush 1B;Ush1b;Usher syndrome 1B
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Buffer:PBS with 0.05% sodium azide and 50% glycerol, PH7.4
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Clonality:Polyclonal
Conjugation:Unconjugated
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