Peroxidase Activity Assay Kit (Colorimetric)
Product Description
Specifications
| Size | 1 Plate Kit, 2 Plate Kit, 5 Plate Kit |
| Compatible Sample Types | Cell Culture Supernatants, Plasma, Serum, Tissue Lysates, Cell Lysates, Urine |
| Quantitative/Semi-Quantitative | Quantitative |
| Solid Support | 96-well Microplate |
| Method Of Detection | Colorimetric |
| Research Area | Inflammation, Oxidative Stress |
| Shipping Type | Blue ice |
| Storage | 2-8°C |
Introduction
Peroxidases, a group of heme-containing enzymes, catalyze oxidation-reduction reactions. They utilize hydrogen peroxide (H2O2) or lipid peroxides as substrates for various oxidative reactions. Peroxidases are present in bacteria, fungi, plants, and animals, and they play a crucial role in protecting cells from oxidative damage.
Peroxidase Activity Assay Kit offers a straightforward, reproducible, and highly sensitive method for measuring peroxidase activity in plasma, serum, cell lysates, urine, and other biological liquid samples without requiring any pre-treatment. In this assay, an ultra-sensitive colorimetric probe reacts with both hydrogen peroxide (H2O2) and peroxidase enzyme to generate a pink-colored product. The intensity of the pink color is then quantified at 570 nm, providing a direct measure of the peroxidase content in the sample.
Kit Components
| Component | Size / Description |
|---|---|
| Microplates | A 96-well (12 strips x 8 wells) plate |
| Assay Diluent | 25 ml |
| Peroxidase (Horseradish Peroxidase) Standard | 1 amber vial (Lyophilized) |
| Hydrogen Peroxide | 1 vial (20 μL of 8.82M) |
| Ultra Colorimetric Probe | 1 amber vial |
Additional Materials Required
- Microplate reader capable of measuring absorbance at 570 nm
- Precision pipettes to deliver 2 µL to 1 mL volumes
- Multi-channel pipettes to deliver 20 μL to 200 μL volumes
- Tubes to prepare sample dilutions
- 15 mL conical tubes
Assay Procedure Summary
Each peroxidase standard and sample should be assayed in duplicate or triplicate. A freshly prepared standard curve should be used each time the assay is performed.
- Add 50 µL of the diluted Horseradish Peroxidase standards or unknown samples to each well of the Microplate.
- Add 50 µL of the Chromogenic Working Solution to each well. Incubate the plate at room temperature for 30 minutes gently mixing in the dark.
- Measure the absorbance at 570nm using a plate reader.








