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Method and Application of Improving Detection Specificity of Immunological Reagent

A technology of immune detection and reagents, applied in the field of in vitro diagnostic reagents, can solve problems such as unfavorable cost control, immature technology, and expensive dosage of blocking substances

Active Publication Date: 2019-06-25
SHANGHAI KEHUA BIO ENG
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

At present, in addition to mouse monoclonal antibodies, there are also rabbit monoclonal antibodies, but the preparation process of rabbit monoclonal antibodies is not mature, and only a few companies have the production capacity of this antibody, and the price is very expensive
[0008] 3. Adding a higher concentration of irrelevant free mouse monoclonal antibody to the reagent reduces the detection value through the method of competitive inhibition
First of all, the composition of commercial blocking substances is not fully disclosed, and it is not known whether the confidential components in the reagent will affect the test results of other types of special samples
Second, commercial blocking substances are only effective for some special samples
Furthermore, such blocking substances are often expensive and used in large quantities, which is not conducive to the cost control of reagent manufacturers in large-scale production.
[0010] To sum up, in the immunoassay reagents with double monoclonal antibody sandwich method to detect antigen as the reaction system, if the sample contains HAMA or RF, it is very easy to produce false positive results, which brings certain risks to clinical diagnosis and doctor's prescription. troubled
At present, the commonly used solutions in the industry either have poor performance, which affects the performance of diagnostic reagents; or the process is immature and cannot be stably and repeatedly produced; or the cost is relatively high, which is a heavy burden on the enterprise.

Method used

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  • Method and Application of Improving Detection Specificity of Immunological Reagent
  • Method and Application of Improving Detection Specificity of Immunological Reagent
  • Method and Application of Improving Detection Specificity of Immunological Reagent

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0094] Murine monoclonal antibodies, pepsin-treated murine monoclonal antibodies, and treated murine monoclonal antibodies purified by gel filtration chromatography were prepared as described in Materials and Methods above. These samples were subjected to SDS-PAGE electrophoresis and the electrophoresis results are shown in figure 1 . In the figure, lane M is the polymer marker, and the molecular weights from top to bottom are 97.2KD, 66.4KD, 44.3KD, 29.0KD, 20.1KD; lanes 1-6 are the antibodies collected at different times during gel filtration chromatography; Lane 7 is the intact mouse monoclonal antibody; lane 8 is the antibody retention sample that has been verified to have better detection results; lane 9 is the antibody that has been treated with pepsin and has not been purified by gel filtration.

[0095] Specifically, in the electrophoresis map, the band near 66.4KD is the complete long chain of mouse monoclonal antibody, the band near 44.3KD is the long chain of mouse...

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Abstract

The invention provides a method for immuno-detection. According to the method, pepsin is utilized first to treat a murine monoclonal antibody, and then the treated murine monoclonal antibody is utilized to perform immuno-detection. The immuno-detection method provided by the invention significantly reduces false positive results of the immuno-detection. Moreover, by using a diluent provided by the invention, the detection value of a false positive sample can be further reduced, and the biological stability of a maker of the treated murine monoclonal antibody, preserved at a working concentration, can be improved. The diluent is a 4-(2-hydroxyerhyl)piperazine-1-ethanesulfonic acid buffer solution, and contains casein, magnesium sulfate and a compound enzyme stabilizer DPD, and the pH value is adjusted to 7.0-8.0 by using a sodium hydroxide solution.

Description

technical field [0001] The present invention relates to the field of in vitro diagnostic reagents. Specifically, the present invention relates to a method for improving the detection specificity of an immunoreagent and its application. Background technique [0002] In vitro diagnostic reagents refer to reagents, kits, calibrators (substances), quality control substances (substances), etc. used for in vitro detection of human samples (various body fluids, cells, tissue samples, etc.). A doctor's prescription for medication is a very important reminder. [0003] Among in vitro diagnostic reagents, the immunological method based on double antibody sandwich technology is a very commonly used method for detecting antigens, and is widely used in enzyme-linked immunosorbent assay, colloidal gold method, and chemiluminescence reagents. Among the raw materials of various double-antibody sandwich detection reagents, murine monoclonal antibodies (hereinafter referred to as murine mon...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): G01N33/577G01N33/535G01N33/533G01N33/532
CPCG01N33/532G01N33/533G01N33/535G01N33/577
Inventor 夏泽张巍佳沈丹李基
Owner SHANGHAI KEHUA BIO ENG
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