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TNNC1 Antibody (monoclonal) (M01)
Mouse monoclonal antibody raised against a full length recombinant TNNC1.
- SPECIFICATION
- CITATIONS
- PROTOCOLS
- BACKGROUND
Application 
| WB, IHC, E |
|---|---|
| Primary Accession | P63316 |
| Other Accession | BC030244 |
| Reactivity | Human |
| Host | mouse |
| Clonality | Monoclonal |
| Isotype | IgG1 kappa |
| Clone Names | 1F8-A9 |
| Calculated MW | 18403 Da |
| Gene ID | 7134 |
|---|---|
| Other Names | Troponin C, slow skeletal and cardiac muscles, TN-C, TNNC1, TNNC |
| Target/Specificity | TNNC1 (AAH30244, 1 a.a. ~ 161 a.a) full-length recombinant protein with GST tag. MW of the GST tag alone is 26 KDa. |
| Dilution | WB~~1:500~1000 |
| Format | Clear, colorless solution in phosphate buffered saline, pH 7.2 . |
| Storage | Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing. |
| Precautions | TNNC1 Antibody (monoclonal) (M01) is for research use only and not for use in diagnostic or therapeutic procedures. |
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Provided below are standard protocols that you may find useful for product applications.
Background
Troponin is a central regulatory protein of striated muscle contraction, and together with tropomyosin, is located on the actin filament. Troponin consists of 3 subunits: TnI, which is the inhibitor of actomyosin ATPase; TnT, which contains the binding site for tropomyosin; and TnC, the protein encoded by this gene. The binding of calcium to TnC abolishes the inhibitory action of TnI, thus allowing the interaction of actin with myosin, the hydrolysis of ATP, and the generation of tension. Mutations in this gene are associated with cardiomyopathy dilated type 1Z.
References
Hypertrophic cardiomyopathy-linked mutation D145E drastically alters calcium binding by the C-domain of cardiac troponin C. Swindle N, et al. Biochemistry, 2010 Jun 15. PMID 20459070.Circulating immunoreactive cardiac troponin forms determined by gel filtration chromatography after acute myocardial infarction. Bates KJ, et al. Clin Chem, 2010 Jun. PMID 20378771.A dilated cardiomyopathy troponin C mutation lowers contractile force by reducing strong myosin-actin binding. Dweck D, et al. J Biol Chem, 2010 Jun 4. PMID 20371872.Coding sequence rare variants identified in MYBPC3, MYH6, TPM1, TNNC1, and TNNI3 from 312 patients with familial or idiopathic dilated cardiomyopathy. Hershberger RE, et al. Circ Cardiovasc Genet, 2010 Apr. PMID 20215591.Effect of calcium-sensitizing mutations on calcium binding and exchange with troponin C in increasingly complex biochemical systems. Tikunova SB, et al. Biochemistry, 2010 Mar 9. PMID 20128626.
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