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Standard solutions and other related products designed to calibrate, monitor the performance, and ensure the accuracy of clinical chemistry-based diagnostics and instrumentation.
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Troponin I (TnI) along with TnT and TnC forms the troponin complex in striated muscle where TnI inhibits actin-myosin interactions mediating muscle relaxation The TnI subfamily includes TnI-skeletal-fast-twitch TnI-skeletal-slow-twitch and TnI-cardiac with this gene encoding the cardiac isoform expressed only in cardiac muscle Mutations in this gene cause familial hypertrophic cardiomyopathy type 7 (CMH7) and familial restrictive cardiomyopathy (RCM) TnI is a key diagnostic marker for heart failure ischemic heart disease and acute myocardial injury including in COVID-19 patients where elevated levels indicate increased mortality risk particularly in those with pre-existing cardiovascular conditions
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Troponin I (TnI) is one of three subunits of the troponin complex in striated muscle, acting as the inhibitory component that blocks actin-myosin interactions to mediate muscle relaxation. This gene encodes the cardiac-specific isoform, expressed exclusively in heart tissue. Mutations are linked to familial hypertrophic cardiomyopathy type 7 (CMH7) and restrictive cardiomyopathy (RCM). TnI is a key biomarker for diagnosing heart failure and ischemic heart disease. Elevated troponin levels are also used to detect acute myocardial injury in moderate to severe COVID-19 cases and are associated with increased mortality in cardiovascular patients hospitalized with COVID-19.
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2.0 g/L and 3.2 g/L Ethanol Standard solutions for use with YSI 2700, 2900 Series and 7100 Analyzers. Kit contains 3 bottles of 2.0 g/L standard and 2 bottles of 3.2 g/L standard.
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This gene encodes the cardiac isoform of troponin T. The encoded protein is the tropomyosin-binding subunit of the troponin complex, which is located on the thin filament of striated muscles and regulates muscle contraction in response to alterations in intracellular calcium ion concentration. Mutations in this gene have been associated with familial hypertrophic cardiomyopathy as well as with dilated cardiomyopathy.
Encompass Procurement Services Non-distribution item offered as a customer accommodation; additional freight charges may apply. Learn More
Small and Specialty Supplier Partner Small and/or specialty supplier based on Federal laws and SBA requirements. Learn More
This gene encodes the cardiac isoform of troponin T. The encoded protein is the tropomyosin-binding subunit of the troponin complex, which is located on the thin filament of striated muscles and regulates muscle contraction in response to alterations in intracellular calcium ion concentration. Mutations in this gene have been associated with familial hypertrophic cardiomyopathy as well as with dilated cardiomyopathy.
Encompass Procurement Services Non-distribution item offered as a customer accommodation; additional freight charges may apply. Learn More