Cell-based Assays

Comet Assay Kit (3-Well Slides) is a single cell gel electrophoresis test (SCGE), rapid and sensitive detection of cell DNA damage kit.

Mitochondrial Permeability Transition Pore Assay Kit s a more direct detection method for detecting the opening of MPTP than only based on mitochondrial membrane potential analysis

CheKine™ Micro Glucose-6-Phosphatase (G6P) Activity Assay Kit is designed to detect the Glucose-6-Phosphatase (G6P) Activity

CheKine™ Micro Phosphoenolpyruvate Carboxykinase (PEPCK) Activity Assay Kit provides a simple, convenient and rapid method for PEPCK activity detection, which is suitable for testing animal and plant tissues, cells, bacteria, serum (plasma) and other samples

CheKine™ Micro Blood Phosphate Assay Kit is designed to detect the Blood Phosphate

CheKine™ Micro Tissue Inorganic Phosphorus  Assay Kit is designed to detect the Tissue Inorganic Phosphorus

CheKine™ Micro Glutamate Synthase (GOGAT) Assay Kit provides a simple, convenient and rapid GOGAT activity detection method, which is suitable for the detection of animal and plant tissue, cell, bacteria, serum, plasma and other samples. The detection principle is that GOGAT uses NADH as the electron donor to catalyze the amino transfer of glutamine to α-ketoglutaric acid to form two-molecule glutamate. The decreasing rate of NADH absorbance in 340 nm can reflect the GOGAT activity.

CheKine™ Micro Glutamic Acid Dehydrogenase (GDH) Assay Kit provides a simple, convenient and rapid GDH activity detection method, which is suitable for the detection of animal and plant tissue, cell, bacteria, serum, plasma and other samples. The detection principle is that GDH catalyzes NH4 + , NADH and α-ketoglutaric acid to produce glutamic acid and NAD+ , which leads to the decrease of absorbance of 340 nm. By measuring the decreasing rate of absorbance of 340 nm, the activity of GDH is calculated.

CheKine™ Micro Water and Soil Nitrite Content Assay Kit provides a simple, convenient and rapid method for the determination of nitrite content, which is suitable for water and soil samples. The detection principle is that under acidic conditions, nitrite reacts with p-aminobenzene sulfonic acid to form diazo compounds, and then reacts with Nmuri 1-naphthyl ethylenediamine to form purplish red azo compounds with a characteristic absorption peak at 540 nm.