Human Myosin VI (MYO6) ELISA Kit | MYO6 elisa kit
Human Myosin VI (MYO6) ELISA Kit
NCBI and Uniprot Product Information
NCBI Description
This gene encodes a reverse-direction motor protein that moves toward the minus end of actin filaments and plays a role in intracellular vesicle and organelle transport. The protein consists of a motor domain containing an ATP- and an actin-binding site and a globular tail which interacts with other proteins. This protein maintains the structural integrity of inner ear hair cells and mutations in this gene cause non-syndromic autosomal dominant and recessive hearing loss. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2014]
Uniprot Description
MYO6: a molecular motor involved in intracellular vesicle and organelle transport. It is one of the so-called unconventional myosins.
Protein type: Motility/polarity/chemotaxis; Motor; Actin-binding
Chromosomal Location of Human Ortholog: 6q13
Cellular Component: Golgi apparatus; nuclear membrane; microvillus; lysosomal membrane; cytoplasmic membrane-bound vesicle; clathrin coated vesicle membrane; coated pit; cell cortex; clathrin-coated endocytic vesicle; DNA-directed RNA polymerase II, holoenzyme; cytosol; nucleoplasm; filamentous actin; ruffle; membrane; cell soma; apical part of cell; axon; endocytic vesicle; perinuclear region of cytoplasm; cytoplasm; unconventional myosin complex; plasma membrane; nucleus
Molecular Function: calmodulin binding; actin filament binding; minus-end directed microfilament motor activity; protein binding; motor activity; ADP binding; actin binding; ATP binding
Biological Process: response to drug; inner ear morphogenesis; DNA damage response, signal transduction by p53 class mediator; actin filament-based movement; metabolic process; regulation of synaptic plasticity; endocytosis; regulation of secretion; locomotory behavior; auditory receptor cell differentiation; synaptic transmission; intracellular protein transport; sensory perception of sound; synaptogenesis; glutamate secretion; dendrite development; positive regulation of transcription from RNA polymerase II promoter; protein targeting
Disease: Deafness, Autosomal Recessive 37; Deafness, Autosomal Dominant 22
Research Articles on MYO6
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Product Notes
The Human MYO6 myo6 (Catalog #AAA7228995) is an ELISA Kit and is intended for research purposes only. The product is available for immediate purchase. The AAA7228995 ELISA Kit recognizes Human MYO6. It is sometimes possible for the material contained within the vial of "Myosin VI (MYO6), ELISA Kit" to become dispersed throughout the inside of the vial, particularly around the seal of said vial, during shipment and storage. We always suggest centrifuging these vials to consolidate all of the liquid away from the lid and to the bottom of the vial prior to opening. Please be advised that certain products may require dry ice for shipping and that, if this is the case, an additional dry ice fee may also be required.Precautions
All products in the AAA Biotech catalog are strictly for research-use only, and are absolutely not suitable for use in any sort of medical, therapeutic, prophylactic, in-vivo, or diagnostic capacity. By purchasing a product from AAA Biotech, you are explicitly certifying that said products will be properly tested and used in line with industry standard. AAA Biotech and its authorized distribution partners reserve the right to refuse to fulfill any order if we have any indication that a purchaser may be intending to use a product outside of our accepted criteria.Disclaimer
Though we do strive to guarantee the information represented in this datasheet, AAA Biotech cannot be held responsible for any oversights or imprecisions. AAA Biotech reserves the right to adjust any aspect of this datasheet at any time and without notice. It is the responsibility of the customer to inform AAA Biotech of any product performance issues observed or experienced within 30 days of receipt of said product. To see additional details on this or any of our other policies, please see our Terms & Conditions page.Item has been added to Shopping Cart
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