| NACRES | NA.84 |
|---|---|
| UNSPSC Code | 12161503 |
| usage | sufficient for 200 colorimetric or fluorometric tests |
| species reactivity | Drosophila, human, mouse |
| packaging | pkg of 1 kit |
| storage condition | dry at room temperature |
| technique(s) | activity assay: suitable |
| accession no. | NM_000167.6 |
| application(s) | cosmeticsenvironmentalfood and beverages |
| detection method | colorimetric |
| relevant disease(s) | cancer |
| shipped in | dry ice |
| storage temp. | −20°C |
| Gene Information | Drosophila ... Gpdh1(33824) human ... GK(2710 ) mouse ... Gpd1(14555) |
| input | food(s) beverage(s) biological sample(s) |
Answer:It supports absorbance at 570 nm and fluorescence at approximately 535 nm excitation and 587 nm emission. The chosen detection mode determines the calibration range and required plate reader.
Answer:The colorimetric range is 10–1,000 µM, while the fluorometric range is 2–50 µM. Samples above these ranges should be diluted and their reported results corrected for the dilution factor.
Answer:The kit is designed for approximately 200 tests in 96-well plates. It includes the enzymatic reaction reagents and glycerol standard, while microplates and a compatible plate reader are supplied separately.
The Sigma-Aldrich Glycerol Assay Kit measures free glycerol in biological samples, foods, beverages, and pharmaceutical formulations using a coupled enzymatic reaction. Glycerol kinase and glycerol phosphate oxidase generate a detectable reaction product with a signal proportional to glycerol concentration. The assay supports colorimetric measurements at 570 nm across 10–1,000 µM glycerol and fluorometric measurements at approximately 535 nm excitation and 587 nm emission across 2–50 µM. The kit provides enough reagents for approximately 200 tests in a 96-well format and includes an assay buffer, dye reagent, enzyme mix, glycerol standard, and ATP. A suitable plate reader and microplates are required separately. Biological culture supernatants, plasma, and formulated samples may require dilution or matrix-specific optimization before measurement. Store reagents at −20°C, protect from light, and minimize repeated freeze–thaw cycles. Colorimetric and fluorescence workflows share the enzymatic principle but have different working concentration ranges.
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