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HCV (hepatitis C virus) cracking agent, preparation method thereof and HCV detection kit

A lysing agent and virus technology, applied in the field of biology, can solve the problems of lack of hepatitis C core antigen-antibody complex, high detection sensitivity, low detection sensitivity, etc., and achieve the effects of easy popularization, improved sensitivity, and simple operation.

Pending Publication Date: 2021-10-26
AUTOBIO DIAGNOSTICS CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

At present, there are two main forms of detection markers for HCV core antigen detection kits reported, one is HCV free core antigen detection, this detection method does not need to lyse the sample, but the detection sensitivity is low; the other is HCV total core antigen detection, this method requires pretreatment of the sample, and the detection sensitivity is high, currently adopted by most manufacturers
However, HCV total core antigen often exists in the form of a complex with antibodies, which needs to be lysed for detection to ensure high detection sensitivity. However, there is still a lack of effective cleavage of HCV core antigen-antibody complexes. sample diluent

Method used

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  • HCV (hepatitis C virus) cracking agent, preparation method thereof and HCV detection kit
  • HCV (hepatitis C virus) cracking agent, preparation method thereof and HCV detection kit
  • HCV (hepatitis C virus) cracking agent, preparation method thereof and HCV detection kit

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Effect test

Embodiment 1

[0032] The preparation of embodiment 1 HCV virus lysing agent of the present invention

[0033] Using purified water as solvent, the concentration of each component is as follows: Tris 2.428wt‰, NaCl 9.25wt‰, NaN 3 2wt‰, Tween 20 0.5wt‰, bromocresol violet 25wt‰, N,N-dimethyl-N-(3-sulfopropyl)-1-octadecyl ammonium inner salt 11wt‰, urea 2M, cleaning antibody 200μg / ml, Casein 3wt‰, BSA 3wt‰, SDS 15wt‰.

[0034] Preparation method: take anionic surfactant (SDS), nonionic surfactant (N,N-dimethyl-N-(3-sulfopropyl)-1-octadecyl ammonium inner salt), protein sedimentation agent (urea), protective protein (BSA / Casein), cleaning antibody, Tris, NaCl, NaN 3 , Tween20 and bromocresol violet are mixed with purified water to obtain the HCV virus lysing agent.

Embodiment 2

[0035] The preparation of embodiment 2 HCV virus lysing agents of the present invention

[0036] Using purified water as solvent, the concentration of each component is as follows: Tris 2.428wt‰, NaCl 9.25wt‰, NaN 32wt‰, Tween 20 0.5wt‰, bromocresol violet 25wt‰, N,N-dimethyl-N-(3-sulfopropyl)-1-octadecyl ammonium inner salt 5wt‰, urea 4M, cleaning antibody 200μg / ml, Casein 3wt‰, BSA 3wt‰, SDS 7wt‰.

[0037] Preparation method: take anionic surfactant (SDS), nonionic surfactant (N,N-dimethyl-N-(3-sulfopropyl)-1-octadecyl ammonium inner salt), protein sedimentation agent (urea), protective protein (BSA / Casein), cleaning antibody, Tris, NaCl, NaN 3 , Tween20 and bromocresol violet are mixed with purified water to obtain the HCV virus lysing agent.

Embodiment 3

[0038] Embodiment 3 Preparation of HCV virus lysing agent of the present invention

[0039] Using purified water as solvent, the concentration of each component is as follows: Tris 2.428wt‰, NaCl 9.25wt‰, NaN 3 2wt‰, Tween 20 0.5wt‰, bromocresol violet 25wt‰, N,N-dimethyl-N-(3-sulfopropyl)-1-octadecyl ammonium inner salt 5wt‰, urea 4M, cleaning antibody 200μg / ml, Casein 3wt‰, BSA 3wt‰, SDS 20wt‰.

[0040] Preparation method: take anionic surfactant (SDS), nonionic surfactant (N,N-dimethyl-N-(3-sulfopropyl)-1-octadecyl ammonium inner salt), protein sedimentation agent (urea), protective protein (BSA / Casein), cleaning antibody, Tris, NaCl, NaN 3 , Tween20 and bromocresol violet are mixed with purified water to obtain the HCV virus lysing agent.

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Abstract

The invention relates to the technical field of biological detection and particularly relates to an HCV (hepatitis C virus) cracking agent, a preparation method thereof and an HCV detection kit. The HCV virus cracking agent comprises an anionic surfactant, a nonionic surfactant, a protein settling agent, protective protein and a cleaning antibody, wherein the nonionic surfactant is N, N-dimethyl-N-(3-sulfopropyl)-1-octadecane ammonium inner salt. The HCV virus splitting agent can effectively split the virus and dissociate an antigen-antibody complex, so sensitivity of detecting the core antigen of the HCV virus is obviously improved, and the probability of illness state delay caused by leak detection in a window period is greatly reduced; the method has advantages of simplicity and rapidness in operation, low cost, high applicability and easiness in popularization and application.

Description

technical field [0001] The invention relates to the field of biological technology, in particular to an HCV virus lysing agent, a preparation method thereof, and a HCV virus detection kit. Background technique [0002] Hepatitis C virus, referred to as hepatitis C, is caused by hepatitis C virus (HCV) infection. Most of the infected people will turn to chronic infection, and nearly half of them will develop into chronic hepatitis. Some of them will eventually develop into liver cirrhosis or even Hepatocellular carcinoma (HCC) has a high incidence and mortality. The detection of HCV is of great significance for the early diagnosis of hepatitis C virus infection and the guidance of clinical treatment. However, as a hepatotropic chronic virus, the onset and clinical symptoms of patients with HCV infection are extremely atypical, and subclinical infection is more common. It is easy to cause missed detection. [0003] The methods currently used for HCV detection mainly include:...

Claims

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Application Information

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IPC IPC(8): G01N33/576G01N33/53
CPCG01N33/5767G01N33/5306G01N2333/186
Inventor 晋高伟刘旭王新明吴文娟孙冯博张春莉
Owner AUTOBIO DIAGNOSTICS CO LTD
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