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Last updated: 2023/5/29

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MYO7A monoclonal antibody, clone AFCH-13 

  • Catalog # : MAB22299
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  • Specification
  • Product Description:
  • Rabbit monoclonal antibody raised against synthetic protein of human MYO7A.
  • Immunogen:
  • A synthetic peptide corresponding to human MYO7A.
  • Host:
  • Rabbit
  • Reactivity:
  • Human, Mouse, Rat
  • Specificity:
  • This antibody reacts with human, mouse, rat MYO7A, in native form and recombinant. Superfamily members of MYO7A are not reactive to antibody.
  • Form:
  • Liquid
  • Purification:
  • Affinity purification
  • Isotype:
  • IgG
  • Recommend Usage:
  • Western Blot (1:500-2000)
    The optimal working dilution should be determined by the end user.
  • Storage Buffer:
  • In PBS, 150 mM NaCl, pH 7.4 (50% glycerol, 0.02% sodium azide).
  • Storage Instruction:
  • Store at -20°C.
    Aliquot to avoid repeated freezing and thawing.
  • Note:
  • This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
  • Applications
  • Western Blot (Cell lysate)
  • Western Blot (Cell lysate)
  • Western Blot (cell lysate) analysis of Y-79 cell lysate.
  • Application Image
  • Western Blot (Cell lysate)
  • Western Blot (Cell lysate)
  • enlarge
  • Gene Information
  • Entrez GeneID:
  • 4647
  • Gene Name:
  • MYO7A
  • Gene Alias:
  • DFNA11,DFNB2,MYOVIIA,MYU7A,NSRD2,USH1B
  • Gene Description:
  • myosin VIIA
  • Gene Summary:
  • 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
  • Other Designations:
  • deafness, autosomal dominant 11,deafness, autosomal recessive 2,myosin VIIA (Usher syndrome 1B (autosomal recessive, severe))
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