GeXP quick detection multi-primers and detection method for detecting akabane viruses, bovine viral diarrhea viruses and blue tongue viruses
A technology for bovine viral diarrhea and Akabane disease, applied in the field of biotechnology applications, can solve the problems of inability to meet detection requirements, cumbersome operation, and long measurement cycle.
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[0025] Example 1 Primer Verification
[0026] The singleplex RT-PCR products were analyzed by capillary electrophoresis with GeXP system. The size of the amplified fragments of each target gene was BTV: 306-308bp, AKAV: 267-269bp, BVDV: 349-353bp, and the size of the amplified fragments was consistent with the design.
Embodiment 2
[0027] Example 2 Establishment of Multiplex Detection System and Verification Results of Single Template Specificity
[0028]In the multi-primer detection system, only a specific fragment of a single virus template was amplified in each reaction without cross-reaction, suggesting that this method has strong specificity and can distinguish and distinguish each virus according to the size of the amplified fragment. The results are shown in Figure 1-Figure 4 .
Embodiment 3
[0029] Embodiment 3 multiple detection system single template sensitivity test result
[0030] Using cloned plasmids to transcribe RNA in vitro as a template, the detection limit of each virus was 100 copies / μL.
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