F59

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SKU: F59

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DSHB Data Sheet

Catalog Fields

Clone ID/Product Name: F59
Available to For-Profits: Yes
Alternate Antibody Name:
Gene Symbol: MYH1A
Ab Isotype: MIgG1, kappa light chain
Gene Name:
Antibody Registry ID: AB_528373 
Uniprot ID: Q91352 
RRID:  
Entrez Gene ID: 417309 
Clonality: Monoclonal
Immunogen: Myosin isolated from pectoralis major
Clone:
Immunogen Sequence: Full length protein
Myeloma Strain: P3/NS1.1Ag4-1
Epitope Mapped: Yes
Antigen Name: Myosin heavy chain (all fast isoforms)
Epitope Location or Sequence: a.a. 200-250
Alternate Antigen Name:
Deposit Date: 2/12/2004
Antigen Molecular Weight: ~223 kDa
Depositor: Stockdale, F.E.
Antigen Sequence:
Depositor Institution: Stanford University Medical Center
Antigen Species: Chicken
Depositor Notes: This antibody is specific for myosin heavy chain in fast contracting skeletal muscle and atrial and ventricular myosin heavy chains.
Host Species: mouse
Hybridoma Cells Available (Non-Profit): Yes
Confirmed Species Reactivity: Amphibian, Avian, Canine, Fish, Human, Mouse, Quail, Rabbit, Rat, Shark, Turtle, Xenopus, Zebrafish
Additional Information:
Predicted Species Reactivity:  
Human Protein Atlas:  
Additional Characterization:  
Recommended Applications: Immunofluorescence, Immunohistochemistry, Immunoprecipitation, Western Blot
All cell products contain the antimicrobial ProClin. Click here for additional information.
These hybridomas were created by your colleagues. Please acknowledge the hybridoma contributor and the Developmental Studies Hybridoma Bank (DSHB) in the Materials and Methods of your publications. Please email the citation to us.
For your Materials & Methods section:
F59 was deposited to the DSHB by Stockdale, F.E. (DSHB Hybridoma Product F59)
Storage and Handling Recommendations
Although many cell products are maintained at 4°C for years without loss of activity, shelf-life at 4°C is highly variable. For immediate use, short term storage at 4°C up to two weeks is recommended. For long term storage, divide the solution into volumes of no less than 20 ul for freezing at -20°C or -80°C. The small volume aliquot should provide sufficient reagent for short term use. Freeze-thaw cycles should be avoided. For concentrate or bioreactor products, an equal volume of glycerol, a cryoprotectant, may be added prior to freezing.
Usage Recommendations
The optimal Ig concentration for an application varies by species and antibody affinity. For each product, the antibody titer must be optimized for every application by the end user laboratory. A good starting concentration for immunohistochemistry (IHC), immunofluorescence (IF), and immunocytochemistry (ICC) when using mouse Ig is 2-5 ug/ml. For western blots, the recommended concentration range of mouse Ig 0.2-0.5 ug/ml. In general, rabbit antibodies demonstrate greater affinity and are used at a magnitude lower Ig concentration for initial testing. The recommended concentrations for rabbit Ig are 0.2-0.5 ug/ml (IF, IHC and ICC) and 20-50 ng/ml (WB).

41 References

  • Initial Publication
  • IF References
  • WB References
  • IHC References
  • IP References
  • Epitope Map References
  • All References
  • Initial Publication

    Slow and fast myosin heavy chain content defines three types of myotubes in early muscle cell cultures.
    Stockdale FE
    The Journal of cell biology 101.5 Pt 1 (1985 Nov): 1643-50.

    IF References

    Slow and fast myosin heavy chain content defines three types of myotubes in early muscle cell cultures.
    Stockdale FE
    The Journal of cell biology 101.5 Pt 1 (1985 Nov): 1643-50.

    CKIP-1 regulates mammalian and zebrafish myoblast fusion.
    Goillot E
    Journal of cell science 125.Pt 16 (2012 Aug 15): 3790-800.

    Immortalized myogenic cells from congenital muscular dystrophy type1A patients recapitulate aberrant caspase activation in pathogenesis: a new tool for MDC1A research.
    Miller JB
    Skeletal muscle 3.1 (2013 Dec 6): 28.

    Scube activity is necessary for Hedgehog signal transduction in vivo.
    Currie PD
    Developmental biology 368.2 (2012 Aug 15): 193-202.

    Smyd1b is required for skeletal and cardiac muscle function in zebrafish.
    Du SJ
    Molecular biology of the cell 24.22 (2013 Nov): 3511-21.

    A novel approach to study motor neurons from zebrafish embryos and larvae in culture.
    Feldman EL
    Journal of neuroscience methods 205.2 (2012 Apr 15): 277-82.

    The Popeye domain containing 2 (popdc2) gene in zebrafish is required for heart and skeletal muscle development.
    Brand T
    Developmental biology 363.2 (2012 Mar 15): 438-50.

    Xirp proteins mark injured skeletal muscle in zebrafish.
    Abdelilah-Seyfried S
    PloS one 7.2 (2012): e31041.

    The muscle-specific ubiquitin ligase atrogin-1/MAFbx mediates statin-induced muscle toxicity.
    Lecker SH
    The Journal of clinical investigation 117.12 (2007 Dec): 3940-51.

    Fibronectin is deposited by injury-activated epicardial cells and is necessary for zebrafish heart regeneration.
    Poss KD
    Developmental biology 382.2 (2013 Oct 15): 427-35.

    Myogenic enhancers regulate expression of the facioscapulohumeral muscular dystrophy-associated DUX4 gene.
    Jones TI
    Molecular and cellular biology 34.11 (2014 Jun): 1942-55.

    Restricted expression of cdc25a in the tailbud is essential for formation of the zebrafish posterior body.
    Kimelman D
    Genes & development 28.4 (2014 Feb 15): 384-95.

    In vivo monitoring of cardiomyocyte proliferation to identify chemical modifiers of heart regeneration.
    Poss KD
    Development (Cambridge, England) 140.3 (2013 Feb 1): 660-6.

    Macondo crude oil from the Deepwater Horizon oil spill disrupts specific developmental processes during zebrafish embryogenesis.
    Barresi MJ
    BMC biology 10. (2012 May 4): 40.

    Divergence of zebrafish and mouse lymphatic cell fate specification pathways.
    Schulte-Merker S
    Development (Cambridge, England) 141.6 (2014 Mar): 1228-38.

    [Pathogenetic and legal insurance problems in the demonstration of atypical mycobacteria as cause of occupational diseases].
    Bassermann FJ
    Praxis der Pneumologie 26.12 (1972 Dec): 677-87.

    The myosin co-chaperone UNC-45 is required for skeletal and cardiac muscle function in zebrafish.
    Pilgrim DB
    Developmental biology 303.2 (2007 Mar 15): 483-92.

    Laminin and Matrix metalloproteinase 11 regulate Fibronectin levels in the zebrafish myotendinous junction.
    Henry CA
    Skeletal muscle 6. (2016): 18.

    Acetylcholine and calcium signalling regulates muscle fibre formation in the zebrafish embryo.
    Ashworth R
    Journal of cell science 118.Pt 22 (2005 Nov 15): 5181-90.

    Zebrafish heart regenerates after chemoptogenetic cardiomyocyte depletion.
    Tsang M
    Developmental dynamics : an official publication of the American Association of Anatomists 250.7 (2021 Jul): 986-1000.

    A human Myogenin promoter modified to be highly active in alveolar rhabdomyosarcoma drives an effective suicide gene therapy.
    Zammit PS
    Cancer gene therapy 28.5 (2021 May): 427-441.

    WB References

    Slow and fast myosin heavy chain content defines three types of myotubes in early muscle cell cultures.
    Stockdale FE
    The Journal of cell biology 101.5 Pt 1 (1985 Nov): 1643-50.

    Evolutionarily conserved sequences of striated muscle myosin heavy chain isoforms. Epitope mapping by cDNA expression.
    Stockdale FE
    The Journal of biological chemistry 264.22 (1989 Aug 5): 13122-30.

    The homeobox transcription factor Irxl1 negatively regulates MyoD expression and myoblast differentiation.
    Pan H
    The FEBS journal 281.13 (2014 Jul): 2990-3003.

    Muscle development and differentiation in the urodele Ambystoma mexicanum.
    Grimaldi A
    Development, growth & differentiation 54.4 (2012 May): 489-502.

    Mutations in KLHL40 are a frequent cause of severe autosomal-recessive nemaline myopathy.
    Laing NG
    American journal of human genetics 93.1 (2013 Jul 11): 6-18.

    Age-related changes in isolated mouse skeletal muscle function are dependent on sex, muscle, and contractility mode.
    Tallis J
    American journal of physiology. Regulatory, integrative and comparative physiology 319.3 (2020 Sep 1): R296-R314.

    IHC References

    Slow and fast myosin heavy chain content defines three types of myotubes in early muscle cell cultures.
    Stockdale FE
    The Journal of cell biology 101.5 Pt 1 (1985 Nov): 1643-50.

    Overdose of D-serine Induces Movement Disorder and Neuromuscular Changes of Zebrafish Larvae.
    Chen YH
    Journal of toxicologic pathology 27.1 (2014 Apr): 19-24.

    Toxicity assessments of chalcone and some synthetic chalcone analogues in a zebrafish model.
    Chen YH
    Molecules (Basel, Switzerland) 19.1 (2014 Jan 7): 641-50.

    SCUBE3 (signal peptide-CUB-EGF domain-containing protein 3) modulates fibroblast growth factor signaling during fast muscle development.
    Yang RB
    The Journal of biological chemistry 289.27 (2014 Jul 4): 18928-42.

    The homeobox transcription factor Irxl1 negatively regulates MyoD expression and myoblast differentiation.
    Pan H
    The FEBS journal 281.13 (2014 Jul): 2990-3003.

    Short-term exposure of zebrafish embryos to arecoline leads to retarded growth, motor impairment, and somite muscle fiber changes.
    Kung HN
    Zebrafish 12.1 (2015 Feb): 58-70.

    Heat-shock-mediated conditional regulation of hedgehog/gli signaling in zebrafish.
    Karlstrom R
    Developmental dynamics : an official publication of the American Association of Anatomists 242.5 (2013 May): 539-49.

    Lampreys have a single gene cluster for the fast skeletal myosin heavy chain gene family.
    Watabe S
    PloS one 8.12 (2013): e85500.

    Muscle development and differentiation in the urodele Ambystoma mexicanum.
    Grimaldi A
    Development, growth & differentiation 54.4 (2012 May): 489-502.

    Vincristine and bortezomib cause axon outgrowth and behavioral defects in larval zebrafish.
    Hutson LD
    Journal of the peripheral nervous system : JPNS 17.1 (2012 Mar): 76-89.

    Expression of DUX4 in zebrafish development recapitulates facioscapulohumeral muscular dystrophy.
    Kunkel LM
    Human molecular genetics 22.3 (2013 Feb 1): 568-77.

    Perturbation of cytosolic calcium by 2-aminoethoxydiphenyl borate and caffeine affects zebrafish myofibril alignment.
    Chen YH
    Journal of applied toxicology : JAT 35.3 (2015 Mar): 287-94.

    Mutations in KLHL40 are a frequent cause of severe autosomal-recessive nemaline myopathy.
    Laing NG
    American journal of human genetics 93.1 (2013 Jul 11): 6-18.

    Intestinal mucosa in nephropathic cystinosis.
    Shiloh H
    Journal of pediatric gastroenterology and nutrition 6.3 (1987 May-Jun): 359-64.

    Localization of sarcomeric proteins during myofibril assembly in cultured mouse primary skeletal myotubes.
    Sanger JM
    Anatomical record (Hoboken, N.J. : 2007) 297.9 (2014 Sep): 1571-84.

    Myosin isozyme expression in response to stretch-induced hypertrophy in the Japanese quail.
    Gonyea WJ
    The Anatomical record 228.3 (1990 Nov): 255-61.

    The appearance of acetylated alpha-tubulin during early development and cellular differentiation in Xenopus.
    Klymkowsky MW
    Developmental biology 136.1 (1989 Nov): 104-17.

    Intracellular Calcium Mobilization Is Required for Sonic Hedgehog Signaling.
    Grunwald DJ
    Developmental cell 45.4 (2018 May 21): 512-525.e5.

    Wilms Tumor 1b Expression Defines a Pro-regenerative Macrophage Subtype and Is Required for Organ Regeneration in the Zebrafish.
    Mercader N
    Cell reports 28.5 (2019 Jul 30): 1296-1306.e6.

    IP References

    Evolutionarily conserved sequences of striated muscle myosin heavy chain isoforms. Epitope mapping by cDNA expression.
    Stockdale FE
    The Journal of biological chemistry 264.22 (1989 Aug 5): 13122-30.

    Epitope Map References

    Evolutionarily conserved sequences of striated muscle myosin heavy chain isoforms. Epitope mapping by cDNA expression.
    Stockdale FE
    The Journal of biological chemistry 264.22 (1989 Aug 5): 13122-30.

    All References

    Slow and fast myosin heavy chain content defines three types of myotubes in early muscle cell cultures.
    Stockdale FE
    The Journal of cell biology 101.5 Pt 1 (1985 Nov): 1643-50.

    Overdose of D-serine Induces Movement Disorder and Neuromuscular Changes of Zebrafish Larvae.
    Chen YH
    Journal of toxicologic pathology 27.1 (2014 Apr): 19-24.

    Toxicity assessments of chalcone and some synthetic chalcone analogues in a zebrafish model.
    Chen YH
    Molecules (Basel, Switzerland) 19.1 (2014 Jan 7): 641-50.

    SCUBE3 (signal peptide-CUB-EGF domain-containing protein 3) modulates fibroblast growth factor signaling during fast muscle development.
    Yang RB
    The Journal of biological chemistry 289.27 (2014 Jul 4): 18928-42.

    The homeobox transcription factor Irxl1 negatively regulates MyoD expression and myoblast differentiation.
    Pan H
    The FEBS journal 281.13 (2014 Jul): 2990-3003.

    Short-term exposure of zebrafish embryos to arecoline leads to retarded growth, motor impairment, and somite muscle fiber changes.
    Kung HN
    Zebrafish 12.1 (2015 Feb): 58-70.

    Heat-shock-mediated conditional regulation of hedgehog/gli signaling in zebrafish.
    Karlstrom R
    Developmental dynamics : an official publication of the American Association of Anatomists 242.5 (2013 May): 539-49.

    Lampreys have a single gene cluster for the fast skeletal myosin heavy chain gene family.
    Watabe S
    PloS one 8.12 (2013): e85500.

    Muscle development and differentiation in the urodele Ambystoma mexicanum.
    Grimaldi A
    Development, growth & differentiation 54.4 (2012 May): 489-502.

    Vincristine and bortezomib cause axon outgrowth and behavioral defects in larval zebrafish.
    Hutson LD
    Journal of the peripheral nervous system : JPNS 17.1 (2012 Mar): 76-89.

    Expression of DUX4 in zebrafish development recapitulates facioscapulohumeral muscular dystrophy.
    Kunkel LM
    Human molecular genetics 22.3 (2013 Feb 1): 568-77.

    Perturbation of cytosolic calcium by 2-aminoethoxydiphenyl borate and caffeine affects zebrafish myofibril alignment.
    Chen YH
    Journal of applied toxicology : JAT 35.3 (2015 Mar): 287-94.

    Mutations in KLHL40 are a frequent cause of severe autosomal-recessive nemaline myopathy.
    Laing NG
    American journal of human genetics 93.1 (2013 Jul 11): 6-18.

    Intestinal mucosa in nephropathic cystinosis.
    Shiloh H
    Journal of pediatric gastroenterology and nutrition 6.3 (1987 May-Jun): 359-64.

    Localization of sarcomeric proteins during myofibril assembly in cultured mouse primary skeletal myotubes.
    Sanger JM
    Anatomical record (Hoboken, N.J. : 2007) 297.9 (2014 Sep): 1571-84.

    Myosin isozyme expression in response to stretch-induced hypertrophy in the Japanese quail.
    Gonyea WJ
    The Anatomical record 228.3 (1990 Nov): 255-61.

    The appearance of acetylated alpha-tubulin during early development and cellular differentiation in Xenopus.
    Klymkowsky MW
    Developmental biology 136.1 (1989 Nov): 104-17.

    Intracellular Calcium Mobilization Is Required for Sonic Hedgehog Signaling.
    Grunwald DJ
    Developmental cell 45.4 (2018 May 21): 512-525.e5.

    Wilms Tumor 1b Expression Defines a Pro-regenerative Macrophage Subtype and Is Required for Organ Regeneration in the Zebrafish.
    Mercader N
    Cell reports 28.5 (2019 Jul 30): 1296-1306.e6.

    CKIP-1 regulates mammalian and zebrafish myoblast fusion.
    Goillot E
    Journal of cell science 125.Pt 16 (2012 Aug 15): 3790-800.

    Immortalized myogenic cells from congenital muscular dystrophy type1A patients recapitulate aberrant caspase activation in pathogenesis: a new tool for MDC1A research.
    Miller JB
    Skeletal muscle 3.1 (2013 Dec 6): 28.

    Scube activity is necessary for Hedgehog signal transduction in vivo.
    Currie PD
    Developmental biology 368.2 (2012 Aug 15): 193-202.

    Smyd1b is required for skeletal and cardiac muscle function in zebrafish.
    Du SJ
    Molecular biology of the cell 24.22 (2013 Nov): 3511-21.

    A novel approach to study motor neurons from zebrafish embryos and larvae in culture.
    Feldman EL
    Journal of neuroscience methods 205.2 (2012 Apr 15): 277-82.

    The Popeye domain containing 2 (popdc2) gene in zebrafish is required for heart and skeletal muscle development.
    Brand T
    Developmental biology 363.2 (2012 Mar 15): 438-50.

    Xirp proteins mark injured skeletal muscle in zebrafish.
    Abdelilah-Seyfried S
    PloS one 7.2 (2012): e31041.

    The muscle-specific ubiquitin ligase atrogin-1/MAFbx mediates statin-induced muscle toxicity.
    Lecker SH
    The Journal of clinical investigation 117.12 (2007 Dec): 3940-51.

    Fibronectin is deposited by injury-activated epicardial cells and is necessary for zebrafish heart regeneration.
    Poss KD
    Developmental biology 382.2 (2013 Oct 15): 427-35.

    Myogenic enhancers regulate expression of the facioscapulohumeral muscular dystrophy-associated DUX4 gene.
    Jones TI
    Molecular and cellular biology 34.11 (2014 Jun): 1942-55.

    Restricted expression of cdc25a in the tailbud is essential for formation of the zebrafish posterior body.
    Kimelman D
    Genes & development 28.4 (2014 Feb 15): 384-95.

    In vivo monitoring of cardiomyocyte proliferation to identify chemical modifiers of heart regeneration.
    Poss KD
    Development (Cambridge, England) 140.3 (2013 Feb 1): 660-6.

    Macondo crude oil from the Deepwater Horizon oil spill disrupts specific developmental processes during zebrafish embryogenesis.
    Barresi MJ
    BMC biology 10. (2012 May 4): 40.

    Divergence of zebrafish and mouse lymphatic cell fate specification pathways.
    Schulte-Merker S
    Development (Cambridge, England) 141.6 (2014 Mar): 1228-38.

    [Pathogenetic and legal insurance problems in the demonstration of atypical mycobacteria as cause of occupational diseases].
    Bassermann FJ
    Praxis der Pneumologie 26.12 (1972 Dec): 677-87.

    The myosin co-chaperone UNC-45 is required for skeletal and cardiac muscle function in zebrafish.
    Pilgrim DB
    Developmental biology 303.2 (2007 Mar 15): 483-92.

    Laminin and Matrix metalloproteinase 11 regulate Fibronectin levels in the zebrafish myotendinous junction.
    Henry CA
    Skeletal muscle 6. (2016): 18.

    Acetylcholine and calcium signalling regulates muscle fibre formation in the zebrafish embryo.
    Ashworth R
    Journal of cell science 118.Pt 22 (2005 Nov 15): 5181-90.

    Zebrafish heart regenerates after chemoptogenetic cardiomyocyte depletion.
    Tsang M
    Developmental dynamics : an official publication of the American Association of Anatomists 250.7 (2021 Jul): 986-1000.

    A human Myogenin promoter modified to be highly active in alveolar rhabdomyosarcoma drives an effective suicide gene therapy.
    Zammit PS
    Cancer gene therapy 28.5 (2021 May): 427-441.

    Evolutionarily conserved sequences of striated muscle myosin heavy chain isoforms. Epitope mapping by cDNA expression.
    Stockdale FE
    The Journal of biological chemistry 264.22 (1989 Aug 5): 13122-30.

    Age-related changes in isolated mouse skeletal muscle function are dependent on sex, muscle, and contractility mode.
    Tallis J
    American journal of physiology. Regulatory, integrative and comparative physiology 319.3 (2020 Sep 1): R296-R314.

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