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| Item number | Size | Datasheet | Manual | SDS | Delivery time | Quantity | Price |
|---|---|---|---|---|---|---|---|
| NSJ-FY12576 | 100 µl | - | - |
3 - 10 business days* |
790.00€
|
If you have any questions, please use our Contact Form.
You can also order by e-mail: info@biomol.com
Larger quantity required? Request bulk
You can also order by e-mail: info@biomol.com
Larger quantity required? Request bulk
Rabbit IgG in phosphate buffered saline, pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol,... more
Product information "Anti-MYH2 / Myosin heavy chain 2, clone 32M67"
Rabbit IgG in phosphate buffered saline, pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol, 0.4-0.5mg/ml BSA. MYH2 antibody detects myosin heavy chain 2, encoded by the MYH2 gene. MYH2 is a skeletal muscle myosin isoform expressed in type IIa fast oxidative fibers. Myosin heavy chains are motor proteins that convert ATP hydrolysis into mechanical force, driving actin-based muscle contraction. MYH2 provides intermediate contractile velocity and fatigue resistance, making it a key determinant of muscle performance.MYH2 antibody is widely applied in muscle physiology, pathology, and developmental biology research. Detection of MYH2 expression distinguishes type IIa fibers from other fiber types, supporting studies of muscle composition and plasticity. In clinical research, MYH2 expression patterns are examined in muscular dystrophy, myopathies, and age-related sarcopenia. By detecting MYH2, researchers can assess muscle adaptation to exercise, disease, and therapeutic interventions. Western blot assays detect MYH2 protein in skeletal muscle extracts. Immunohistochemistry maps MYH2 distribution within muscle cross sections, enabling identification of fiber type composition. Immunofluorescence highlights sarcomeric localization, providing high-resolution visualization of contractile architecture.MYH2 mutations cause autosomal dominant myopathy characterized by progressive muscle weakness, abnormal fiber morphology, and impaired contractility. Detection with MYH2 antibody supports genetic and pathological studies of this disease. Additionally, MYH2 is a marker of regenerative fibers and is used to study developmental myogenesis. By applying MYH2 antibody, scientists can investigate both physiological and pathological aspects of skeletal muscle biology.Beyond skeletal muscle, MYH2 research contributes to understanding of biomechanics, metabolic regulation, and aging. Differences in MYH2 expression across individuals and conditions reflect muscle plasticity and adaptation. The antibody therefore provides a critical reagent for both basic science and translational studies in muscle biology.MYH2 antibody from NSJ Bioreagents offers dependable specificity for detecting type IIa myosin heavy chain, supporting high-quality studies of skeletal muscle physiology and disease.
| Keywords: | Anti-MYH2, Anti-Myosin-2, Anti-Myosin heavy chain 2, Anti-Myosin heavy chain 2a, Anti-Myosin heavy chain IIa, Anti-Myosin heavy chain, skeletal muscle, adult 2, MYH2 Antibody / Myosin heavy chain 2 |
| Supplier: | NSJ Bioreagents |
| Supplier-Nr: | FY12576 |
Properties
| Application: | WB |
| Antibody Type: | Monoclonal |
| Clone: | 32M67 |
| Conjugate: | No |
| Host: | Rabbit |
| Species reactivity: | human, mouse, rat |
| Immunogen: | A synthesized peptide derived from human MYH2 |
| Format: | Purified |
Database Information
| KEGG ID : | K24220 | Matching products |
| UniProt ID : | Q9UKX2 | Matching products |
| Gene ID : | GeneID 4620 | Matching products |
Handling & Safety
| Storage: | -20°C |
| Shipping: | -20°C (International: -20°C) |
Caution
Our products are for laboratory research use only: Not for administration to humans!
Our products are for laboratory research use only: Not for administration to humans!
Information about the product reference will follow.
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