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MYO9A encodes a member of the myosin superfamily. Additionally we are shipping Myosin IXA Antibodies (7) and many more products for this protein.
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analysis of actin network self-organization by a monomeric myosin IXa
MYO9A deficiency may affect the presynaptic motor axon, manifesting in congenital myasthenic syndrome.
Vaccinia virus F11 (show F11 Proteins) promotes viral spread by binding to host myosin-9A and inhibit RhoA (show RHOA Proteins) signaling.
Depletion of myosin-IXA in collectively migrating cells led to altered organization of the actin cytoskeleton and tension-dependent disruption of cell-cell adhesions, followed by an inability to form new adhesions resulting in cell scattering.
deletion of the Rho GTPase-activating protein Myo9a in mice causes proximal tubular dilation and fibrosis
Myo9a is a critical regulator of Rho-dependent and -independent signaling mechanisms that guide epithelial differentiation.
This gene encodes a member of the myosin superfamily. The protein represents an unconventional myosin\; it should not be confused with the conventional non-muscle myosin-9 (MYH9). Unconventional myosins contain the basic domains of conventional myosins and are further distinguished from class members by their tail domains. They function as actin-based molecular motors. Mutations in this gene have been associated with Bardet-Biedl Syndrome.
, myosin 9a
, unconventional myosin-9a
, unconventional myosin-IXa
, myr 7