Glutamic-pyruvic Transaminase (GPT) Activity Assay Kit, 50T/24S
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Glutamic-pyruvic Transaminase (GPT) Activity Assay Kit, 50T/24S

Cat.No: AACAK-YJL-0019 Datasheet

Specification Quantities

50T/24S:
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Product Details Product Overview Related Products
Product Name Glutamic-pyruvic Transaminase (GPT) Activity Assay Kit, 50T/24S
Catalog No. AACAK-YJL-0019
Detection Method Visible spectrophotometry, Spectrophotometer
Storage Store at 2-8°C, 6 months
Intended Use For research use only.
Note For your safety and health, please wear lab coat, disposable gloves and mask during operation.
Product Introduction Glutamic-pyruvic transaminase (GPT), also known as alanine aminotransferase (ALT), catalyzes the reversible transfer of an amino group from alanine to α-ketoglutarate, producing pyruvate and glutamate. ALT is predominantly found in the liver cytosol, and its release into the bloodstream is a highly specific and sensitive indicator of hepatocellular damage. Measuring ALT activity is a cornerstone of liver function tests in both clinical diagnostics and preclinical toxicology studies. This kit employs a kinetic UV assay that monitors the oxidation of NADH coupled to the pyruvate produced by ALT.
Product Application • Clinical and research assessment of liver health and hepatocellular injury.
• Preclinical drug safety evaluation (hepatotoxicity screening).
• Studies of liver diseases such as hepatitis, NAFLD/NASH, and cirrhosis.
• Monitoring liver damage in models of ischemia-reperfusion or toxin exposure.
Product Advantages • Kinetic Assay for Accuracy: Continuously monitors the reaction rate, providing superior accuracy over fixed-time endpoint methods and minimizing interference.
• High Sensitivity: The coupled lactate dehydrogenase (LDH) reaction provides signal amplification, enabling detection of low levels of ALT activity.
• Optimized for Serum/Plasma: Specifically formulated for direct use with clinical samples, requiring minimal sample volume and no complex pre-treatment.
• Correlates with Standard Methods: Calibrated to deliver results consistent with international reference procedures (IFCC), ensuring data comparability.

For research use only, not for clinical use.

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