MYOZ2 (Myozenin 2) is a Protein Coding gene. Diseases associated with MYOZ2 include Cardiomyopathy, Hypertrophic, 16 and Myoz2-Related Familial Hypertrophic Cardiomyopathy. GO annotations related to this gene include actin binding and telethonin binding. An important paralog of this gene is MYOZ1.The protein encoded by this gene belongs to a family of sarcomeric proteins that bind to calcineurin, a phosphatase involved in calcium-dependent signal transduction in diverse cell types. These family members tether calcineurin to alpha-actinin at the z-line of the sarcomere of cardiac and skeletal muscle cells, and thus they are important for calcineurin signaling. Mutations in this gene cause cardiomyopathy familial hypertrophic type 16, a hereditary heart disorder.
Stoccaggio: Store at -20℃ Valid for 12 months. Avoid freeze / thaw cycles.
Isotipo: IgG
Clonalità: Polyclonal
Coniugazione: Unconjugated
Applicazione: IHC
Diluizione: IHC 1:40-1:200
Simbolo target: MYOZ2
Ig target: C4orf5;Calcineurin binding protein calsarcin 1;Calsarcin 1;Calsarcin-1;Calsarcin1;CMH16;CS 1;CS1;FATZ related protein 2;FATZ-related protein 2;Muscle specific protein;MYOZ 2;MYOZ2;MYOZ2;Myozenin-2;Myozenin2
Area di ricerca:Cardiovascular;Signal Transduction
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