MYH7 antibody [MSVA-464M] HistoMAX(tm)
GTX04970
ApplicationsImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
ReactivityHuman
TargetMYH7
Overview
- SupplierGeneTex
- Product NameMYH7 antibody [MSVA-464M] HistoMAX(tm)
- Delivery Days Customer7
- Application Supplier NoteIHC-P: 1:100 - 1:200. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
- ApplicationsImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
- CertificationResearch Use Only
- ClonalityMonoclonal
- Clone IDMSVA-464M
- Concentration66.66 ug/ml
- ConjugateUnconjugated
- Gene ID4625
- Target nameMYH7
- Target descriptionmyosin heavy chain 7
- Target synonymscardiac muscle myosin heavy chain 7 beta; CMD1S; CMH1; MPD1; MYHCB; myHC-beta; myhc-slow; myopathy, distal 1; myosin 7; myosin heavy chain beta-subunit; myosin, heavy chain 7, cardiac muscle, beta; myosin, heavy polypeptide 7, cardiac muscle, beta; myosin-7; rhabdomyosarcoma antigen MU-RMS-40.7A; SPMD; SPMM
- HostMouse
- IsotypeIgG2b
- Protein IDP12883
- Protein NameMyosin-7
- Scientific DescriptionMuscle myosin is a hexameric protein containing 2 heavy chain subunits, 2 alkali light chain subunits, and 2 regulatory light chain subunits. This gene encodes the beta (or slow) heavy chain subunit of cardiac myosin. It is expressed predominantly in normal human ventricle. It is also expressed in skeletal muscle tissues rich in slow-twitch type I muscle fibers. Changes in the relative abundance of this protein and the alpha (or fast) heavy subunit of cardiac myosin correlate with the contractile velocity of cardiac muscle. Its expression is also altered during thyroid hormone depletion and hemodynamic overloading. Mutations in this gene are associated with familial hypertrophic cardiomyopathy, myosin storage myopathy, dilated cardiomyopathy, and Laing early-onset distal myopathy. [provided by RefSeq, Jul 2008]
- ReactivityHuman
- Storage Instruction-20°C or -80°C,2°C to 8°C
- UNSPSC12352203