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No. 52 Chengliu Road, Jiading District, Shanghai
Shanghai Yansheng Industrial Co., Ltd
No. 52 Chengliu Road, Jiading District, Shanghai
Product Details:
Soil lignin peroxidase(SLiP) Test BoxMeasurement significance
Lignin peroxidase(EC1.11.1.14) is a peroxidase containing heme, belonging to the lignin degrading enzyme system. It has great potential for applications in lignin biodegradation, papermaking industry, textile industry, aromatic compound conversion and degradation, and environmental pollution control.
Measurement principle
Lignin peroxidase oxidizes resveratrol to produce veratrol aldehyde, which is produced inThere is a characteristic absorption peak at 310nm.
Bring your own experimental supplies and instruments
Balance, low-temperature centrifuge, UV spectrophotometer/ELISA reader, trace quartz colorimetric dish/96 well plate (UV plate).
Reagent composition and preparation:
Reagent 1: Liquid1 bottle, stored at 4 ℃.
Reagent 2: Liquid1 bottle, stored at 4 ℃.
Reagent 3: Powder1 bottle (brown), stored at 4 ℃ in the dark. Add 667 μ L anhydrous ethanol before use, cover tightly and mix well. Then add 9.333 mL distilled water and mix well. Store in the dark.
Reagent 4: Powder1 tube, stored in the dark at 4 ℃. Add 1 mL of distilled water before use and dissolve thoroughly.
Standard product: Powder1 bottle, add 10 mL of distilled water before use, fully dissolve. 1 μ mol/mL standard solution, stored at 4 ℃ in the dark.
Product attributes:
Item Number |
specification |
detection method |
YSH3435 |
100 tubes/48 samples |
Micro method |
YSH3435-1 |
50 tubes/24 samples |
UV spectrophotometry |


Measurement operation:
Preheat the spectrophotometer/ELISA reader for 30 minutes, adjust the wavelength to 570 nm, and zero the distilled water.
2. Blank tube: Take an EP tube and add 10 μ L of distilled water, 100 μ L of reagent 2, 100 μ L of reagent 3, and 10 μ L of reagent 4. Mix well and cover tightly with a bottle cap (to prevent water loss). Place the tube in a boiling water bath for 15 minutes. After cooling, invert the EP tube several times and measure the absorbance value at 570nm, which is recorded as an empty white tube A. After color development, it is necessary to complete the measurement within 30 minutes.
3. Standard tube: Take an EP tube and add 10 μ L of standard substance, 100 μ L of reagent 2, 100 μ L of reagent 3, and 10 μ L of reagent 4. Mix well and cover tightly with a bottle cap (to prevent moisture loss). Place the tube in a boiling water bath for 15 minutes. After cooling, invert the EP tube several times and measure the absorbance value at 570nm, which is recorded as the A standard tube. After color development, it is necessary to complete the measurement within 30 minutes.
4. Measurement tube: Take an EP tube, add 10 μ L of supernatant, 100 μ L of reagent 2, 100 μ L of reagent 3, and 10 μ L of reagent 4, mix well, and cover tightly with a bottle cap (to prevent water loss). Place in a boiling water bath for 15 minutes, cool down, and repeatedly invert the EP tube several times. Measure the absorbance value at 570nm and record it as the A measurement tube. After color development, it is necessary to complete the measurement within 30 minutes.
Note: Blank tubes and standard tubes only need to be measured once.
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