Anti-MYO7A Antibody

CAT: 0519-A03915-2Size: 100 µLDry Ice: NoHazardous: No
CAT#:0519-A03915-2Size:100 µL
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Background
MYO7A, also named a USH1B, is one of myosins protein which are actin-based motor molecules with ATPase activity. Unconventional myosins serve in intracellular movements. Their highly divergent tails are presumed to bind to membranous compartments, which would be moved relative to actin filaments. In retina, MYO7A might play a role in trafficking of ribbon-synaptic vesicle complexes and renewal of the outer photoreceptors disks. In inner ear, it might maintain the rigidity of stereocilia during the dynamic movements of the bundle. It is involved in hair-cell vesicle trafficking of aminoglycosides, which are known to induce ototoxicity. Defects in MYO7A are the cause of Usher syndrome type 1B (USH1B) . Defects in MYO7A are the cause of deafness autosomal recessive type 2 (DFNB2) . Defects in MYO7A are the cause of deafness autosomal dominant type 11 (DFNA11) . The antibody is specific to MYO7A.
Description
Boster Bio Anti-MYO7A Antibody catalog # A03915-2. Tested in WB, IHC, ICC/IF, ELISA. This antibody reacts with Human, Mouse, Rat.
Gene Name
MYO7A
UniProt
Q13402
Host
Rabbit
Reactivity
Human, Mouse, Rat
Immunogen
Peptide
Clonality
Polyclonal
Applications
WB, IHC, ICC/IF, ELISA
Purification
Immunogen affinity purified.
Concentration
500 μg/mL
Form
Liquid
Storage Conditions
12 months from date of receipt, -20°C as supplied. 6 months 2 to 8°C after reconstitution. Avoid repeated freezing and thawing.
Contents
500 μg/mL antibody with PBS,0.02% NaN3, 1 mg BSA and 50% glycerol.

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