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KTN1 encodes an integral membrane protein that is a member of the kinectin protein family. Additionally we are shipping Kinectin 1 (Kinesin Receptor) Proteins (4) and many more products for this protein.
Showing 10 out of 20 products:
Human Polyclonal KTN1 Primary Antibody for WB - ABIN4894920
Choudhury, Liu, Clark, Pang: Caspase-7: a critical mediator of optic nerve injury-induced retinal ganglion cell death. in Molecular neurodegeneration 2015
Human Polyclonal KTN1 Primary Antibody for ICC, IF - ABIN4328867
Stadler, Hjelmare, Neumann, Jonasson, Pepperkok, Uhlén, Lundberg: Systematic validation of antibody binding and protein subcellular localization using siRNA and confocal microscopy. in Journal of proteomics 2012
Chicken Polyclonal KTN1 Primary Antibody for WB - ABIN2782098
Olsen, Blagoev, Gnad, Macek, Kumar, Mortensen, Mann: Global, in vivo, and site-specific phosphorylation dynamics in signaling networks. in Cell 2006
Kinectin is concentrated in the perinuclear sheets of the endoplasmic reticulum by interacting with polysomes. Kinectin may play a role in determinining the morphology of the endoplasmic reticulum.
Kinectin may have the ability to anchor mRNAs to the surface of the endoplasmic reticulum.
The kinesin-1 deficiency weakened intercellular adhesion, despite the maintenance of adherens junctions and other desmosome components at the plasma membrane.
The genes identified KTN1, ROCK1 (show ROCK1 Antibodies), and ZAK (show ZAK Antibodies) may be responsible for loss of cellular homeostasis in giant cells tumors of bone
kinectin is markedly enriched at integrin-based adhesion complexes, induced by clustering integrins with fibronectin (show FN1 Antibodies)-coated beads
The data suggests that both KNT and KNTvd4(-) participate in microtubule-dependent secretion of amylin (show IAPP Antibodies) in islet beta-cells.
anchoring the elongation factor-1 complex onto endoplasmic reticulum via EF-1delta/kinectin interaction is important for regulating protein synthesis in eukaryotic cells
When kinesin binds with both heads to the microtubule, the neck linkers in the rear and forward heads extend forward and backward. This supports the notion that neck linker movements accompany the 'hand-over-hand' motion of the two motor domains.
A large number of variations were found in many of the genes (myozenin 1, gamma-filamin, kinectin-1) in patients with limb-girdle muscular dystrophies and controls.
The presence of coiled-coil domains in the ktn1/ret (show RET Antibodies) fusion protein (PTC8) suggests ligand-independent dimerization and thus constitutive activation of the ret (show RET Antibodies) tyrosine kinase (show TXK Antibodies) domain.
This gene encodes an integral membrane protein that is a member of the kinectin protein family. The encoded protein is primarily localized to the endoplasmic reticulum membrane. This protein binds kinesin and may be involved in intracellular organelle motility. This protein also binds translation elongation factor-delta and may be involved in the assembly of the elongation factor-1 complex. Alternate splicing results in multiple transcript variants of this gene.
, CG-1 antigen
, kinesin receptor