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IHC-P analysis of mouse skeletal muscle tissue using GTX32147 MYH3 antibody. Working concentration : 5 microg/ml
IHC-P analysis of mouse skeletal muscle tissue using GTX32147 MYH3 antibody. Working concentration : 5 microg/ml
IHC-P analysis of mouse skeletal muscle tissue using GTX32147 MYH3 antibody. Working concentration : 5 microg/ml

MYH3 antibody

GTX32147
GeneTex
ApplicationsWestern Blot, ELISA, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
ReactivityHuman, Mouse, Rat
TargetMYH3
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Overview

  • Supplier
    GeneTex
  • Product Name
    MYH3 antibody - Overexpression Validated
  • Delivery Days Customer
    9
  • Antibody Specificity
    MYH3 antibody is predicted to not cross-react with other members of the myosin heavy chain family.
  • Application Supplier Note
    WB: 1 microg/mL. IHC-P: 5 microg/mL. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Western Blot, ELISA, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    1 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID4621
  • Target name
    MYH3
  • Target description
    myosin heavy chain 3
  • Target synonyms
    CPSFS1A; CPSFS1B; CPSKF1A; CPSKF1B; DA2A; DA2B; DA2B3; DA8; HEMHC; MYHC-EMB; MYHSE1; myosin heavy chain, fast skeletal muscle, embryonic; myosin, heavy chain 3, skeletal muscle, embryonic; myosin, heavy polypeptide 3, skeletal muscle, embryonic; myosin, skeletal, heavy chain, embryonic 1; myosin-3; SMHCE
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDP11055
  • Protein Name
    Myosin-3
  • Scientific Description
    Myosin is a major contractile protein which converts chemical energy into mechanical energy through the hydrolysis of ATP. Myosin is a hexameric protein composed of a pair of myosin heavy chains (MYH) and two pairs of nonidentical light chains. This gene is a member of the MYH family and encodes a protein with an IQ domain and a myosin head-like domain. Mutations in this gene have been associated with two congenital contracture (arthrogryposis) syndromes, Freeman-Sheldon syndrome and Sheldon-Hall syndrome. [provided by RefSeq, Jul 2008]
  • Reactivity
    Human, Mouse, Rat
  • Storage Instruction
    2°C to 8°C
  • UNSPSC
    12352203

References

  • Mutation of the MYH3 gene causes recessive cleft palate in Limousine cattle.
    Read more
  • A postnatal role for embryonic myosin revealed by MYH3 mutations that alter TGFbeta signaling and cause autosomal dominant spondylocarpotarsal synostosis. Zieba J et al., 2017 Feb 16, Sci Rep
    Read more