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These observations support the notion that a major function of Myosin VI in the nerve terminal is tethering synaptic vesicles to proper sub-cellular location within the bouton
These data demonstrate that generating an organized and functional actin (show ACTB Antibodies) structure in this cell requires multiple activities coordinated by myosin VI.
The androcam structure and its binding to the myosin VI structural (Insert 2) and regulatory (IQ) light chain sites are distinct from those of calmodulin.
data indicate that myosin V (show MYO5A Antibodies) and VI, but not II, play related but distinct roles in regulating microtubule (MT)-based mitochondrial movement: they oppose, rather than complement, protracted MT-based movements and perhaps facilitate organelle docking
MyoVI is required for border cell migration where it stabilizes E-cadherin (show CDH1 Antibodies) and Arm.
Myosin VI is crucial for correct cell morphology and maintenance of adhesive cellular contacts within epithelial cell layers.
Myosin VI stabilizes a branched actin network in actin structures (cones) that mediate the separation of the syncytial spermatids. I
The spatial and temporal expression of Myosin VI was examined by expressing a Green Fluorescent Protein tagged Myosin VI molecule, under the control of a Myosin VI-Gal4 (show LGALS4 Antibodies) line.
Data suggest that Echinoid mediates the dimerization of myosin VI/Jaguar in vivo which in turn regulates the reorganization and/or contraction of actin (show ACTB Antibodies) filaments to control changes in cell shape.
Miranda protein forms an apical crescent at interphase, but is ubiquitously localized at prophase in a Myosin-II-dependent manner.
MYO6 could play an essential role in the growth of OSCC cells via regulation of cell cycle progression and apoptosis.
characterisation of the human myosin VI deafness mutant (R1166X) suggests that defects in cargo binding may leave myosin VI in a primed/activated state with an increased actin-binding ability
PRAS40 (show AKT1S1 Antibodies) was downregulated in the DU145 cells following MYO6 knockdown.
knockdown of MYO6 slightly arrested cell cycle in G0/G1 phase, but remarkably increased the proportion of the sub-G1 phase of cell with the increase of apoptotic cells in colorectal cancer
study indicates that MYO6 may play an important role in gastric cancer tumorigenesis and may serve as a potential therapeutic target in human gastric cancer.
This study identified an isoform-specific regulatory helix, named the alpha2-linker, that defines specific conformations and hence determines the target selectivity of human myosin VI.
Interaction of myosin VI and its binding partner DOCK7 plays an important role in NGF-stimulated protrusion formation in PC12 cells.
Knockdown of myosin VI significantly suppressed melanoma cell viability and proliferation.
Knockdown of MYO6 markedly reduced cell viability and colony formation, as well as suppressed cell cycle progression in breast cancer cells.
MYO6 was highly expressed in hepatocellular carcinoma.
indicated that decreased MYO6 levels in ksv/ksv mutants disrupt actin networks in the apical region of hair cells, thereby maintaining the normal structure of the cuticular plates and rootlets, and additionally provided a cellular basis for stereociliary fusion in Myo6 mutants
We propose that myosin VI, by removing stereociliary elements such as CDH23 (show CDH23 Antibodies) as a component of the transient lateral links (which are probably required for the integrity of the immature hair bundles), allows the hair bundle and its transduction apparatus to progress in their development, so that the mechano-electrical transducer channels acquire their physiological resting tension and Ca2 (show CA2 Antibodies)+-dependent adaptation properties
a plaque accretion defect as the primary manifestation of myosin VI loss in Cx43 (show GJA1 Antibodies) homeostasis, is reported.
the Turner mutation was mapped to a critical region of 11 cM on chromosome 9 that includes myosin VI.
Myo1a (show MYO1A Antibodies) and Myo6 play essential roles in response to intestinal mucosal injury
Disruption in optineurin (show OPTN Antibodies) and myosin VI-mediated cellular trafficking is associated with amyotrophic lateral sclerosis.
We postulate that this novel interaction linking MVI with the PKA pathway could be important for targeting AKAP9 (show AKAP9 Antibodies)-PKA complex within cells and/or providing PKA to phosphorylate MVI tail domain.
Dysfunction of myosin VI is associated with slow retinal optic neuropathy and age-related macular degeneration.
homologous pairing and myosin VI-mediated transcriptional pause release account for the rapid and efficient expression of genes induced by an external stimulus
Myosin VI mediates the movement of NHE3 (show SLC9A3 Antibodies) to the microvillus in intestinal epithelial cells.
Data suggest that cells direct the movement of vesicles around a cell by altering the relative number of myosin Va (show MYO5A Antibodies) from Gallus gallus and myosin VI from Sus scrofa.
A myosin VI deafness mutation, D179Y, uncoupled the release of the ATP hydrolysis product, inorganic phosphate (Pi), from dependency on actin binding and destroyed the ability of single dimeric molecules to move processively on actin filaments.
model reveals that myosin VI, unlike plus-end directed myosins, does not use a pure lever arm mechanism, but instead steps with a mechanism analogous to the kinesin neck-linker uncoupling mode
The stepping dynamics of single quantum-dot-labeled myoV and myoVI motors linked to a common cargo, was studied.
These results suggest that myosin VI kinetics are tuned such that the motor maintains a consistent level of mechanical tension within the cell, a property potentially shared by other mechanosensitive proteins.
a mechanism is proposed of myosin VI stepping that predicts a regulation through load of the motor's roles as transporter and anchor
2.4-A structure of a truncated version of the reverse-direction myosin motor, myosin VI, that contains the motor domain and binding sites for two calmodulin molecules
Data demonstrate that full-length myosin VI is capable of forming stable, processive dimers when monomers are clustered, which move up to 1-2 mum in approximately 30 nm, hand-over-hand steps.
further adaptations within the motor increase the magnitude and variability of the plus-end directed converter movements, and unexpectedly provide the source of the highly variable myosin VI step size
Results suggest that myosin VI and vinculin (show VCL Antibodies) form a molecular apparatus that generates cohesive cell-cell contacts in cultured mammalian epithelia.
MVI, but not myosins IB or IIB, was detected in chromaffin granules isolated from bovine medulla and found to be tightly associated with the granule apical surface.
This gene encodes a protein involved intracellular vesicle and organelle transport, especially in the hair cell of the inner ear. Mutations in this gene have been found in patients with non-syndromic autosomal dominant and recessive hearing loss.
, 95F unconventional myosin
, myosin 95F
, myosin VI
, myosin heavy chain
, myosin heavy chain at 95F
, unconventional myosin VI
, unconventional myosin-6
, unconventional myosin-VI
, Snell's waltzer
, unconventional myosin