Method for detecting concentration of horseradish peroxidase by utilizing water-soluble InP/ZnS QDs probe

A horseradish peroxidase and probe detection technology, which is applied in measuring devices, fluorescence/phosphorescence, and material analysis through optical means, can solve problems such as limited applications, achieve low detection limits, simple and convenient detection processes, and high sensitivity high effect

Active Publication Date: 2016-07-20
铜陵华兴精细化工有限公司
View PDF4 Cites 4 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Therefore, traditional IIB-VI quantum dots such as CdTe, CdSe, etc., although their technical development is rela

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Method for detecting concentration of horseradish peroxidase by utilizing water-soluble InP/ZnS QDs probe
  • Method for detecting concentration of horseradish peroxidase by utilizing water-soluble InP/ZnS QDs probe

Examples

Experimental program
Comparison scheme
Effect test

Example Embodiment

[0026] Example 1

[0027] 1. Establish a linear relationship

[0028] Prepare the original solution of horseradish peroxidase of different concentrations, and add the same volume of water-soluble InP / ZnSQDs, namely water-soluble indium phosphide / zinc sulfide quantum dots, and then dilute to 3mL with phosphate buffer solution to prepare A series of equal-volume standard solutions of horseradish peroxidase with different concentrations. The concentration of horseradish peroxidase in several standard solutions is different, and the concentration of water-soluble InP / ZnSQDs is the same. Among them, the concentration of horseradish peroxidase in the standard solution The concentration is 0, 7×10 -9 mol / L, 1.5×10 -8 mol / L, 2.5×10 -8 mol / L、3×10 -8 mol / L、6×10 -8 mol / L, 1×10 -7 mol / L, 2×10 -7 mol / L and 4×10 -7 mol / L, its numbers are a, b, c, d, e, f, g, h, and i respectively, and the concentration of water-soluble InP / ZnSQDs in the standard solution is 23.04nM;

[0029] After the water-solub...

Example Embodiment

[0033] Example 2

[0034] A method for detecting the concentration of horseradish peroxidase using water-soluble InP / ZnSQDs probe, including:

[0035] Step 1. Prepare different concentrations of water-soluble InP / ZnSQDs-containing horseradish peroxidase standard solutions, detect the fluorescence intensity of the standard solution, obtain the fluorescence spectrum of the standard solution, and establish that the horseradish peroxidase concentration is zero The linear relationship between the difference between the fluorescence intensity of the standard solution and the fluorescence intensity of all standard solutions and the concentration of horseradish peroxidase, such as figure 2 Shown

[0036] Step 2: Prepare a sample solution of horseradish peroxidase containing water-soluble InP / ZnSQDs, detect the fluorescence intensity of the sample solution, and determine the concentration of horseradish peroxidase in the sample solution through the linear relationship.

[0037] In the method...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

No PUM Login to view more

Abstract

The invention discloses a method for detecting concentration of horseradish peroxidase by utilizing a water-soluble InP/ZnS QDs probe. The method comprises the following steps: step 1, preparing horseradish peroxidase standard solutions which have different concentration and contain water-soluble InP/ZnS QDs; detecting the fluorescence intensity of the standard solutions to obtain fluorescence spectrograms of the standard solutions; establishing a linear relation of a difference value between the fluorescence intensity of the standard solution with the concentration of the horseradish peroxidase of zero and the fluorescence intensity of all the standard solutions and the concentration of the horseradish peroxidase; step 2, preparing a horseradish peroxidase sample solution containing the water-soluble InP/ZnS QDs and detecting the fluorescence intensity of the standard solution; and determining the concentration of the horseradish peroxidase in the sample solution through the linear solution. By taking the InP/ZnS QDs as the probe and utilizing the property of quenching the fluorescence of the water-soluble InP/ZnS QDs of the horseradish peroxidase, the concentration of the horseradish peroxidase is detected; and a detection process is simple and convenient, high in sensitivity and low in detection limit, and online and in-situ rapid and sensitive detection of the concentration of the horseradish peroxidase can be realized.

Description

technical field [0001] The invention relates to a method for detecting the concentration of horseradish peroxidase, in particular to a method for detecting the concentration of horseradish peroxidase by using a water-soluble InP / ZnSQDs probe. Background technique [0002] Horseradish peroxidase is a glycoprotein, the origin of its name is because of the high content of the enzyme in horseradish, it is currently the most widely used labeling enzyme, used to label antibodies or other proteins, both It can be used for positioning detection and also for quantitative determination. Horseradish peroxidase is widely used in the fields of industry, agriculture, medicine, and environmental protection. It can be used to prepare biochemical diagnostic kits for blood sugar, triglycerides, and cholesterol, as well as enzyme-labeled antibody performance in ELISA assays. [0003] In recent years, with the continuous advancement of quantum dot synthesis technology and the deepening of the ...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
IPC IPC(8): G01N21/64
CPCG01N21/6402G01N21/6486
Inventor 黄珊肖琦王鲁敏黄初升苏炜崔建国
Owner 铜陵华兴精细化工有限公司
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products