Use a colorimetric assay kit to measure the concentration of pyruvate in the test samples, and carry out duplex examinations.
Add 10 microliters of the test samples to different wells of a 96-well plate, and add 90 microliters of working reagent to each sample. Incubate covered for 30 minutes at room temperature. Then, place the plate in a microplate reader to measure the absorbance of each well at 570 nanometers.
Plot the pyruvate standard curve and calculate the pyruvate concentrations from the standard curve by multiplying each concentration by 2.25.
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