MYO7A monoclonal antibody, clone AFCH-13
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More Files
- More Functions
Western Blot (Cell lysate)
Western Blot (cell lysate) analysis of Y-79 cell lysate.
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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.
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Applications
Western Blot (Cell lysate)
Western Blot (cell lysate) analysis of Y-79 cell lysate. -
Gene Info — MYO7A
Entrez GeneID
4647Protein Accession#
Q13402Gene Name
MYO7A
Gene Alias
DFNA11, DFNB2, MYOVIIA, MYU7A, NSRD2, USH1B
Gene Description
myosin VIIA
Gene Ontology
HyperlinkGene 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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Interactome
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Disease
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