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MYO7A Rabbit anti-Human, Mouse, Rat, Polyclonal, Proteintech

Rabbit Polyclonal Antibody
Supplier: Proteintech Group Inc 207201AP150UL

Description
The antibody is specific to MYO7A.
Myosin VIIa is a member of the myosin superfamily of actin-based motor proteins. Defects in the myosin VIIa gene are responsible for hearing impairment in shaker-1 (sh1) mice and causes Usher syndrome IB in humans. Usher syndrome associates congenital deafness, vestibular dysfunction, and retinitis pigmentosa and is the most common form of combined deafness and blindness. Structural features of myosin VIIa protein include an ATP binding N-terminal motor domain, a central region which possess five light-chain binding (IQ) motifs, and a C-terminal domain with three myosin tail homology (MyTH4) and talin-like homology regions.Specifications
MYO7A | |
Polyclonal | |
Unconjugated | |
MYO7A | |
DFNA11, DFNB2, MYO7A, myosin VIIA, MYOVIIA, MYU7A, NSRD2, USH1B | |
Rabbit | |
Antigen Affinity Chromatography | |
RUO | |
17921, 266714, 4647 | |
-20°C | |
Liquid |
Immunocytochemistry, Immunofluorescence, Western Blot | |
0.29 mg/mL | |
PBS with 50% glycerol and 0.02% sodium azide; pH 7.3 | |
P97479, Q13402 | |
Myo7a | |
Peptide | |
150 μL | |
Primary | |
Human, Mouse, Rat | |
Antibody | |
IgG |
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