catalog number :
MBS422444
products full name :
Goat anti-MYO5A Antibody
products short name :
MYO5A
products name syn :
MYO5A; myosin VA (heavy chain 12, myoxin); GS1; MYH12; MYO5; MYR12; dilute; myosin V; myosin VA; myosin, heavy polypeptide kinase; myoxin; dilute antibody; GS1 antibody; MYH12 antibody; MYO5 antibody; myosin V antibody; myosin VA antibody; myosin VA (heavy chain 12; myoxin) antibody; myosin; heavy polypeptide kinase antibody; myoxin antibody; MYR12 antibody; MYO5A antibody
other names :
unconventional myosin-Va isoform 1; Unconventional myosin-Va; unconventional myosin-Va; myosin VA; Dilute myosin heavy chain, non-muscle; Myosin heavy chain 12; Myosin-12; Myoxin
products gene name :
MYO5A
other gene names :
MYO5A; MYO5A; GS1; MYO5; MYH12; MYR12; MYH12
uniprot entry name :
MYO5A_HUMAN
reactivity :
Tested: Human, Mouse; Expected from sequence similarity: Human, Mouse, Rat, Cow
purity :
Purified from goat serum by ammonium sulphate precipitation followed by antigen affinity chromatography using the immunizing peptide
form :
Supplied at 0.5 mg/ml in Tris saline, 0. 02% sodium azide, pH7.3 with 0.5% bovine serum albumin.
concentration :
100ug specific antibody in 200ul
storage stability :
Aliquot and store at -20 degree C. Minimize freezing and thawing.
tested application :
Peptide ELISA (EIA), Western Blot (WB), Immunofluorescence (IF)
app notes :
Peptide ELISA: Antibody detection limit dilution 1: 8000. Western Blot: Approx 200kDa band observed in lysates of cell line Jurkat (calculated MW of 215kDa according to NP_000250.3). Recommended concentration: 1-3ug/ml. Immunofluorescence: Transverse sections of Mouse Skeletal Muscle shows staining of the fibre membrane and neuromuscular junction. The observed pattern corresponds to earlier findings in literature with different antibodies (Röder et al, Proc Natl Acad Sci U S A.2010 Feb 2;107(5): 2031-6; PMID: 20133847). Recommended concentration: 1-3ug/ml.
other info1 :
Immunogen: Peptide with sequence C-ETKQLELDLN, from the internal region of the protein sequence according to NP_000250.3; NP_001135967.1. Epitope: Internal region
other info2 :
Note: This antibody is expected to recognize both reported isoforms (NP_000250.3; NP_001135967.1).
ncbi acc num :
NP_000250.3
ncbi gb acc num :
NM_000259.3
ncbi mol weight :
218,608 Da
ncbi pathways :
Fcgamma Receptor (FCGR) Dependent Phagocytosis Pathway (1269279); Immune System Pathway (1269170); Innate Immune System Pathway (1269203); Insulin Processing Pathway (1268747); Membrane Trafficking Pathway (1269877); Metabolism Of Proteins Pathway (1268677); Peptide Hormone Metabolism Pathway (1268746); Regulation Of Actin Dynamics For Phagocytic Cup Formation Pathway (1269281); Translocation Of GLUT4 To The Plasma Membrane Pathway (1269896); Vesicle-mediated Transport Pathway (1269876)
ncbi summary :
This gene is one of three myosin V heavy-chain genes, belonging to the myosin gene superfamily. Myosin V is a class of actin-based motor proteins involved in cytoplasmic vesicle transport and anchorage, spindle-pole alignment and mRNA translocation. The protein encoded by this gene is abundant in melanocytes and nerve cells. Mutations in this gene cause Griscelli syndrome type-1 (GS1), Griscelli syndrome type-3 (GS3) and neuroectodermal melanolysosomal disease, or Elejalde disease. Multiple alternatively spliced transcript variants encoding different isoforms have been reported, but the full-length nature of some variants has not been determined. [provided by RefSeq, Dec 2008]
uniprot summary :
MYO5A: Processive actin-based motor that can move in large steps approximating the 36-nm pseudo-repeat of the actin filament. Involved in melanosome transport. May also be required for some polarization process involved in dendrite formation. May be a homodimer, which associates with multiple calmodulin or myosin light chains. Binds MLPH and MYRIP. Interacts with RIPL2, the interaction is required for its role in dendrite formation. Detected in melanocytes. 3 isoforms of the human protein are produced by alternative splicing. Protein type: Motility/polarity/chemotaxis; Motor. Chromosomal Location of Human Ortholog: 15q21. Cellular Component: actin filament; actomyosin; cell soma; cytoplasm; cytosol; early endosome; endoplasmic reticulum; filopodium tip; Golgi apparatus; growth cone; intermediate filament; late endosome; lysosome; melanosome; membrane; myosin complex; neuron projection; peroxisome; photoreceptor outer segment; recycling endosome; ruffle; vesicle. Molecular Function: actin binding; ATP binding; calcium ion binding; calmodulin binding; microfilament motor activity; Rab GTPase binding. Biological Process: actin filament-based movement; cellular response to insulin stimulus; ER localization; exocytosis; insulin secretion; locomotion during locomotory behavior; long-chain fatty acid biosynthetic process; melanin biosynthetic process; melanocyte differentiation; melanosome transport; myelination; odontogenesis; post-Golgi vesicle-mediated transport; regulation of inositol-1,4,5-triphosphate receptor activity; secretory granule localization; synapse organization and biogenesis; synaptic transmission; transport; vesicle transport along actin filament; vesicle-mediated transport; visual perception. Disease: Griscelli Syndrome, Type 1