The MYO15A polyclonal antibody (PAC064315) is a powerful tool for researchers studying the MYO15A protein, an important molecular motor involved in actin-based cell motility and maintenance of cell shape. This antibody, produced in rabbits, demonstrates high reactivity with human samples and has been validated for use in Western blot applications. By specifically binding to the MYO15A protein, researchers can accurately detect and analyze its expression in a variety of cell types, making it an essential tool for studies in cell biology and developmental biology.MYO15A is a vital component in various cellular processes, including cell migration, cytokinesis, and intracellular transport.
Dysregulation of MYO15A has been associated with diseases such as hereditary hearing loss and developmental disorders. Understanding the role of MYO15A in these conditions is crucial for developing targeted therapies and interventions.With its high specificity and sensitivity, the MYO15A polyclonal antibody offers researchers a reliable and effective means of investigating the function and localization of MYO15A in different cellular contexts. Whether studying normal cell function or disease pathology, this antibody is a valuable tool for advancing our understanding of MYO15A biology and its implications for human health.
Antibody Name:
MYO15A Antibody (PACO64315)
Antibody SKU:
PACO64315
Size:
50ul
Host Species:
Rabbit
Tested Applications:
ELISA, IHC
Recommended Dilutions:
IHC:1:200-1:500
Species Reactivity:
Human
Immunogen:
Recombinant Human Unconventional myosin-XV protein (237-451AA)
IHC image of PACO64315 diluted at 1:200 and staining in paraffin-embedded human brain tissue performed on a Leica BondTM system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a Goat anti-rabbit polymer IgG labeled by HRP and visualized using 0.05% DAB.
Background:
Myosins are actin-based motor molecules with ATPase activity. Unconventional myosins serve in intracellular movements. Their highly divergent tails are presumed to bind to membranous compartments, which would be moved relative to actin filaments. Required for the arrangement of stereocilia in mature hair bundles (By similarity).
Myosins are actin-based motor molecules with ATPase activity. Unconventional myosins serve in intracellular movements. Their highly divergent tails are presumed to bind to membranous compartments, which would be moved relative to actin filaments. Required for the arrangement of stereocilia in mature hair bundles ().
UniProt Protein Details:
NCBI Summary:
This gene encodes an unconventional myosin. This protein differs from other myosins in that it has a long N-terminal extension preceding the conserved motor domain. Studies in mice suggest that this protein is necessary for actin organization in the hair cells of the cochlea. Mutations in this gene have been associated with profound, congenital, neurosensory, nonsyndromal deafness. This gene is located within the Smith-Magenis syndrome region on chromosome 17. Read-through transcripts containing an upstream gene and this gene have been identified, but they are not thought to encode a fusion protein. Several alternatively spliced transcript variants have been described, but their full length sequences have not been determined. [provided by RefSeq, Jul 2008]