NADP+/NADPH Colorimetric Assay Kit (WST-8)

Cat# E-BC-K803-M-96T

Size : 96T

Brand : Elabscience

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Phone : +1 850 650 7790

Detection Principle Detect total content of NADP+ and NADPH:
Glucose 6-phosphate (G6P) is oxidized to 6-phosphate gluconolactone (6-PG) by glucose-6-phosphate dehydrogenase (G6PDH), and NADP+ is reduced to NADPH during this reaction. NADPH, under the action of 1-mPMS, transfer electrons to WST-8 to produce the yellow product, which has a characteristic absorption peak at 450 nm. Therefore, the total content of NADP+ and NADPH can be quantified by measure the OD value at 450 nm.
Detect NADPH:
After treating sample, heat at 60℃ water bath for 30 min. the NADP+ of the sample is decomposed and only NADPH remains. NADPH reduces WST-8 to form Formazan, and the amount of NADPH is determined by measure the OD value at 450 nm.
Detect NADP+ and NADP+/NADPH:
The content of NADP+ and the ratio of NADP+/NADPH in the sample can be obtained according to the total content of NADP+ and NADPH obtained of the first two steps as well as the separate content of NADPH.
Synonyms NADP;NADPH
Sample Type Animal tissue,Cell
Detection Method Colorimetric method
Detection Instrument Microplate reader (450 nm)
Research Area Oxidative Stress ,  Metabolic Diseases ,  Glycolysis And Lipid Metabolism ,  Cuproptosis ,  Disulfidptosis
Other Reagents Required Ultrapure water
Storage This product can be stored at -20°C for 12 months with shading light.
Valid Period 12 months
Sensitivity 0.02 μmol/L
Detection Range 0.02-5.0 μmol/L
Precision inter-assay CV: 5.5% | intra-assay CV: 2.1%
Assay Time 1 h 10 min

The recommended dilution factor for different samples is as follows (for reference only):

Sample Type Dilution Factor
Jurkat cells 1
Mark cells 1
HCT116 cells 1
293T cells 1
10% Mouse kidney tissue homogenate 1
Hela cells 1

The diluent is normal saline (0.9% NaCl) or PBS (0.01 M, pH 7.4). For the dilution of other sample types, please do pretest to confirm the dilution factor.

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