Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
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.
DFNA11; DFNB2; Hdb; motor protein; MyO VIIa; Myo7; Myo7a; myosin; myosin 7a; myosin VIIA; myosin VIIA (Usher syndrome 1B (autosomal recessive, severe)); myosin-VIIa; Myosin-VIIa motor domain; MYOVIIA; MYU7A; nmf371; NSRD2; polka; sh1; sh-1; shaker 1; unconventional myosin-VIIa; USH1B
200 µL
150 µL
100 µL
100 µL
100 µg
100 µL
Searching for an antibody we don't offer? We make custom antibodies for specific targets, species and applications.
More than 18,000 custom antibodies created so far.
Talk to a specialist nowIf an Invitrogen™ antibody doesn't perform as described on our website or datasheet,we'll replace the product at no cost to you, or provide you with a credit for a future purchase.*
Learn moreGet expert recommendations for common problems or connect directly with an on staff expert for technical assistance related to applications, equipment and general product use.
Contact tech support