一种基于CPA-双CISPR / Cas12b检测PVC2病毒的组合物及其检测方法与应用

By optimizing the CPA-dual CISPR/Cas12b system and a specific crRNA concentration ratio, combined with time-resolved immunofluorescence microspheres and lateral flow chromatography strips, the problems of low sensitivity, complex operation, and strong equipment dependence in existing PCV2 virus detection have been solved, achieving rapid, simple, and accurate virus detection.

CN120310964BActive Publication Date: 2026-07-17GUANGDONG MEDICAL UNIV

Patent Information

Authority / Receiving Office
CN · China
Patent Type
Patents(China)
Current Assignee / Owner
GUANGDONG MEDICAL UNIV
Filing Date
2025-05-28
Publication Date
2026-07-17

AI Technical Summary

Technical Problem

Existing PCV2 virus detection methods suffer from low sensitivity, complex operation, strong equipment dependence, high false positive rate, high cost, and difficulty in meeting the needs of rapid diagnosis, making them unsuitable for widespread application in resource-limited grassroots farms or in the field.

Method used

By employing the CPA-dual CISPR/Cas12b system, combining crRNA-2 and crRNA-4 at specific concentration ratios, optimizing the CPA reaction reagents and CRISPR/Cas12b system, and using time-resolved immunofluorescent microspheres and optimized lateral flow chromatography test strips, rapid and convenient PCV2 virus detection can be achieved.

Benefits of technology

It improves detection sensitivity and signal-to-noise ratio, simplifies operation procedures, reduces equipment dependence, is suitable for field use, reduces costs, and achieves rapid and accurate PCV2 virus detection.

✦ Generated by Eureka AI based on patent content.

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Abstract

本发明公开提供了一种基于CPA‑双CISPR / Cas12b检测PVC2病毒的组合物及其检测方法与应用,属于分子生物学检测技术领域。组合物包括核苷酸序列如SEQ ID NO.8所示的crRNA‑2和核苷酸序列如SEQ ID NO.10所示的crRNA‑4,crRNA‑2与crRNA‑4的浓度比为1:1;本发明通过将CPA与CRISPR / Cas12b系统整合于一个体系中,采用双CRISPR / Cas12b系统识别CPA不同扩增产物中的PAM位点,显著增强了AapCas12b的反式活性,进一步提高了检测灵敏度。
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