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Swine fever virus detection method based on G-quadruplex fluorescence characteristic and kit

A technology of swine fever virus and fluorescence characteristics, which is applied in the field of genetic engineering, can solve the problems of high requirements for operators, expensive reagents, and obstacles to application, and achieve the effects of improving detection efficiency, easy operation, and accuracy

Inactive Publication Date: 2015-05-13
GUIZHOU DAXING AGRI SCI & TECH DEV CO LTD +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, this diagnostic method has problems such as expensive reagents, easy contamination, high requirements for operators, and the need for expensive fluorescent quantitative PCR amplification instruments, etc., which seriously hinder its application at the grassroots level.

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0028] The test kit for swine fever virus detection based on G-quadruplex fluorescent properties, which consists of:

[0029] (1) NASBA reaction buffer includes: 40mM Tris-HCl (PH8.0); 70mM KCl; 20mM MgCl2; 1mM deoxyribonucleoside triphosphates (dNTPs); 1mM ribonucleoside triphosphates (NTPs); Sugar Alcohol; 10% Dimethyl Sulfoxide (DMSO).

[0030](2) NASBA forward primer and reverse primer include, 0.5 μM forward primer (E2P7f): ACTATGAGCCCAGGGACAGCTACTT; 0.5 μM reverse primer (E2P7T7r): GTCGACTAATACGACTCACTATAGGGTTCCCTATCAACACTACCTCACCC T.

[0031] (3) NASBA enzyme reaction solution includes: T7 RNA polymerase 60U; AMV reverse transcriptase 5U; RNase (RNAseH) 0.1U, 2μg of BSA.

[0032] (4) The composition of G-quadruplex reaction buffer includes: 10 mM 4-hydroxyethylpiperazineethanesulfonic acid, 200 mM sodium chloride and 20 mM potassium chloride; 1 μM upstream probe and 1 μM downstream probe. Add sterile double distilled water to make up to 97 μl.

[0033] (5) The upstre...

Embodiment 2

[0040] The test kit for swine fever virus detection based on G-quadruplex fluorescent properties, which consists of:

[0041] (1) NASBA reaction buffer includes: 30mM Tris-HCl (PH8.0); 80mM KCl; 10mM MgCl2; 2mM deoxyribonucleoside triphosphates (dNTPs); 0.5mM ribonucleoside triphosphates (NTPs); 5mM disulfide Threitol; 20% Dimethyl Sulfoxide (DMSO).

[0042] (2) NASBA forward primer and reverse primer include, 0.5 μM forward primer (E2P7f): ACTATGAGCCCAGGGACAGCTACTT; 0.5 μM reverse primer (E2P7T7r): GTCGACTAATACGACTCACTATAGGGTTCCCTATCAACACTACCTCACCC T.

[0043] (3) NASBA enzyme reaction solution includes: T7 RNA polymerase 40U; AMV reverse transcriptase 2U; RNase (RNAseH) 0.15U, 5μg of BSA.

[0044] (4) The composition of G-quadruplex reaction buffer includes: 10mM 4-hydroxyethylpiperazineethanesulfonic acid, 200mM sodium chloride and 20mM potassium chloride; upstream probe 2μM and downstream probe 2μM, Add sterile double distilled water to make up to 97μl;

[0045] (5) The...

Embodiment 3

[0052] The test kit for swine fever virus detection based on G-quadruplex fluorescent properties, which consists of:

[0053] (1) NASBA reaction buffer includes: 60mM Tris-HCl (PH8.0); 60mM KCl; 30mM MgCl2; 0.5mM deoxyribonucleoside triphosphates (dNTPs); 2mM ribonucleoside triphosphates (NTPs); 20mM disulfide Threitol; 5% Dimethyl Sulfoxide (DMSO).

[0054] (2) NASBA forward primer and reverse primer include, 1 μM forward primer (E2P7f): ACTATGAGCCCAGGGACAGCTACTT; 1 μM reverse primer (E2P7T7r): GTCGACTAATACGACTCACTATAGGGTTCCCTATCAACACTACCTCACCC T.

[0055] (3) NASBA enzyme reaction solution includes: T7 RNA polymerase 60U; AMV reverse transcriptase 5U; RNase (RNAseH) 0.05U, 0.5μg of BSA.

[0056] (4) The composition of G-quadruplex reaction buffer includes: 10mM 4-hydroxyethylpiperazineethanesulfonic acid, 200mM sodium chloride and 20mM potassium chloride; upstream probe 0.5μM and downstream probe 0.2 μM. Add sterile double distilled water to make up to 97 μl.

[0057] (5...

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PUM

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Abstract

The invention discloses a swine fever virus detection method based on G-quadruplex fluorescence characteristic and a kit, and belongs to the technical field of gene engineering. The method comprises: utilizing a nucleic acid sequence-based amplification (NASBA) technology to amplify target RNA to obtain a single-chain RNA product; adding an upstream probe, a downstream probe and the RNA amplification product into a G- quadruplex fluorescence detection buffer, performing denaturation and annealing, then adding protoporphyrin, and utilizing a microplate reader or fluorophotometer to detect the fluorescence intensity in the reaction system, so as to determine whether the sample possesses a swine fever virus. The method is fast, precise and stable in swine fever virus detection speed, good in reappearance, simple in detection steps and low in cost.

Description

technical field [0001] The invention relates to the technical field of genetic engineering, in particular to a detection method for swine fever virus based on the fluorescence characteristics of G-quadruplex, and a kit used for the detection method for swine fever virus. Background technique [0002] Classical swine fever, also known as classical swine fever, is an acute or chronic, febrile and highly contagious infectious disease of pigs caused by swine fever virus (an RNA virus). Swine fever is distributed worldwide, seriously endangering the development of pig industry. Due to its high hazard, it is an international key quarantine object. In my country, the direct economic loss caused by swine fever reaches several billion yuan every year. At present, the detection methods for CSFV nucleic acid mainly include fluorescent quantitative RT-PCR method. However, this diagnostic method has problems such as expensive reagents, easy contamination, high requirements for opera...

Claims

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Application Information

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IPC IPC(8): C12Q1/70C12Q1/68C12R1/93
CPCC12Q1/6865C12Q1/70C12Q2563/116C12Q2565/514
Inventor 王毅邓明刚鲁小璐
Owner GUIZHOU DAXING AGRI SCI & TECH DEV CO LTD
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