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Myosin VIIa antibody

Catalog Number:OM264524
OM264524
Discount Price
OM264524-100ul
1~2 Week
100ul
OM264524-50ul
50ul
OM264524-20ul
20ul
1~2 Week
Product Profile
Product Name Myosin VIIa antibody
Antibody Type Primary Antibodies
Product description Rabbit polyclonal to Myosin VIIaMyosin 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.
Immunogen Synthetic peptide: S(16)GQEFDVPIGAVVKLC(31).Immunizing peptide corresponds to amino acid residues 16-31 from mouse myosin VIIa. This sequence is completely conserved in mouse, porcine, and human myosin VIIa.
Key Feature
Clonality Polyclonal
Isotype IgG
Host Species Rabbit
Tested Applications ICC/IFIHCIPWB
ICC/IF: 1:50:
Species Reactivity HumanMouseRatGuinea PigBovine
Concentration 1mg/ml (Please refer to the vial label for the specific concentration)
Purification Affinity purified
Target Information
Gene Synonyms DFNA11
DFNB2
MYOVIIA
MYU7A
NSRD2
USH1B
Target Myosin VIIa
Tissue Specificity Detects Myosin VIIa from mouse tissues as well as recombinant.
Application

Application

Western blot of myosin VIIa in mouse testes tissue extract using
Application Notes ICC/IF: 1:50:
Additional Information
Form Liquid
Storage Instructions Upon receipt - Keep as concentrated solution. Aliquot and store at -20ºC or below. Avoid freeze-thaw cycles.
Storage Buffer PBS, 1 mg/ml BSA, 0.05% sodium azide
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