Glutathione peroxidase determination kit, preparation method of glutathione peroxidase determination kit and application of glutathione peroxidase determination kit

A technology of glutathione peroxide and glutathione, which is applied in the direction of biological testing, material inspection products, etc., can solve the problems of cumbersome steps, high price, waste, etc., and achieve improved sensitivity, improved stability, improved The effect of reactivity

Active Publication Date: 2019-01-18
中拓生物有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] At present, the main method for the determination of glutathione peroxidase in China is the Elisa method, which requires manual operation, and the steps are cumbersome, time-consuming, and expensive.
At present, the reagents that can be used in automatic biochemical analysis in China are ultraviolet enzymatic glutathione peroxidase

Method used

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  • Glutathione peroxidase determination kit, preparation method of glutathione peroxidase determination kit and application of glutathione peroxidase determination kit
  • Glutathione peroxidase determination kit, preparation method of glutathione peroxidase determination kit and application of glutathione peroxidase determination kit
  • Glutathione peroxidase determination kit, preparation method of glutathione peroxidase determination kit and application of glutathione peroxidase determination kit

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0039] The components of reagent R1 are: Tris buffer 100mmol / L, EDTA 0.5mmol / L, glutathione reductase 1KU / L, reduced glutathione 5mmol / L, potassium chloride 6g / L, magnesium chloride 0.3g / L, Tween 20 1ml / L, tyrosine 1g / L, sodium azide 0.5g / L;

[0040] The components in reagent R2 are: Tris buffer 100mmol / L, EDTA 0.5mmol / L, NADPH 1mmol / L, cumene hydroperoxide 0.3mmol / L, triton 100 1ml / L, sucrose 5g / L , Sodium azide 0.5g / L.

[0041] The pH value of reagent R1 is 7.0; the pH value of reagent R2 is 9.5;

[0042] Preparation method: (1) Preparation of reagent R1: take an appropriate amount of water, add the raw materials shown in R1 respectively, stir well to dissolve one raw material, then add the next raw material, adjust to the required pH value with hydrochloric acid or sodium hydroxide, and constant volume to required volume. (2) Preparation of reagent R2: Take an appropriate amount of water, add the raw materials shown in R1 respectively, stir well to dissolve one raw mate...

Embodiment 2

[0044] The components of reagent R1 are: Tris buffer 80mmol / L, EDTA 0.8mmol / L, glutathione reductase 1.2KU / L, reduced glutathione 6mmol / L, potassium chloride 8g / L, magnesium chloride 0.4 g / L, Tween 20 1ml / L, sucrose 8g / L, sodium azide 1g / L;

[0045] The components in reagent R2 are: Tris buffer 80mmol / L, EDTA 0.9mmol / L, NADPH 1mmol / L, cumene hydroperoxide 0.3mmol / L, Tween 20 1ml / L, sucrose 8g / L, Sodium azide 1g / L.

[0046] The pH value of reagent R1 is 7.0; the pH value of reagent R2 is 9.8;

[0047] The preparation method of the kit in Example 2 is the same as in Example 1.

Embodiment 3

[0049] The components of reagent R1 are: phosphate buffer 50mmol / L, EDTA 1mmol / L, glutathione reductase 2KU / L, reduced glutathione 5mmol / L, potassium chloride 6g / L, magnesium chloride 0.3g / L, Kao B66 1ml / L, tyrosine 1g / L, sodium azide 0.5g / L;

[0050] The components in reagent R2 are: Tris buffer 50mmol / L, EDTA 1mmol / L, NADPH 1mmol / L, cumene hydroperoxide 0.5mmol / L, Kao B66 1ml / L, sucrose 5g / L, azide Sodium 0.5g / L.

[0051] The pH value of reagent R1 is 7.5; the pH value of reagent R2 is 10.0;

[0052] The preparation method of the kit of Example 3 is the same as that of Example 1.

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Abstract

The invention discloses a glutathione peroxidase determination kit, the kit contains a reagent R1 and a reagent R2; the reagent R1 contains buffer solution, EDTA, glutathione reductase, reduced glutathione, potassium chloride, magnesium chloride, surfactant, stabilizer and preservative; and the reagent R2 contains the buffer solution, the EDTA, NADPH, cumene hydrogen peroxide, surfactant, stabilizer and preservative. The invention also discloses a preparation method of the glutathione peroxidase determination kit and application of the glutathione peroxidase determination kit. The kit providedby the invention is a high-sensitivity and excellently stable liquid kit.

Description

technical field [0001] The invention relates to the technical field of biochemical reagent assay, in particular to a glutathione peroxidase assay kit, and also to a preparation method and application of the glutathione peroxidase assay kit. Background technique [0002] Glutathione peroxidase (GSH-Px) is an important peroxide-decomposing enzyme widely present in the body. The active center of GSH-Px is selenocysteine, and its activity can reflect the selenium level in the body. Selenium is a component of the GSH-Px enzyme system. It can catalyze GSH into GSSG and reduce toxic peroxides to non-toxic hydroxyl compounds, thereby protecting the structure and function of cell membranes from interference and damage by peroxides. The reduction of NADPH is linearly related to the activity of glutathione peroxidase. GSH-Px mainly includes four types: cytoplasmic GSH-Px, plasma GSH-Px, phospholipid hydroperoxide GSH-Px and gastrointestinal specific GSH-Px. Cytoplasmic GSH-Px: a tet...

Claims

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Application Information

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IPC IPC(8): G01N33/68
CPCG01N33/68
Inventor 隗勇刘安娜张强
Owner 中拓生物有限公司
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