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MYO9A encodes a member of the myosin superfamily. Zusätzlich bieten wir Ihnen Myosin IXA Antikörper (7) und Myosin IXA Proteine (2) und viele weitere Produktgruppen zu diesem Protein an.
MYO9A deficiency may affect the presynaptic motor axon, manifesting in congenital myasthenic syndrome.
Vaccinia virus F11 (zeige F11 ELISA Kits) promotes viral spread by binding to host myosin-9A and inhibit RhoA (zeige RHOA ELISA Kits) 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