Primer combination and GeXP detection method for simultaneously identifying 5 bovine viral dermatitis viruses
A primer combination, a technology for bovine viral diarrhea, applied in the directions of microorganism-based methods, biochemical equipment and methods, and the determination/inspection of microorganisms, which can solve problems such as indistinguishability
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Embodiment 1
[0115] Embodiment 1, design and preparation of primer combination
[0116] A large number of sequence analyzes and comparisons were carried out to obtain several primers for the identification of five bovine viral dermatitis viruses: FMDV, BTV, VSV, BVDV and IBRV. Preliminary experiments were carried out on each primer to compare performances such as sensitivity and specificity, and finally 5 pairs of specific primers for identifying 5 kinds of bovine viral dermatitis viruses were obtained. Each specific primer pair, forward primer and reverse primer, consists of a targeting segment and a universal primer segment, with the universal primer segment located 5' to the targeting segment.
[0117] The primer pair used to identify FMDV consists of the following two primers (5'→3'):
[0118] FMDV-F (Sequence 1 of the Sequence Listing): AGGTGACACTATAGAATA GCCGTGGGACCATACAGG;
[0119] FMDV-R (Sequence 2 of the Sequence Listing): GTACGACTCACTATAGGGA AAGTGATCTGTAGCTTGGAATCTC.
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Embodiment 2
[0143] Embodiment 2, specificity
[0144] 1. Single template experiment
[0145] 1. Extract the total RNA of the sample to be tested and reverse transcribe it into cDNA. The samples to be tested are: FMDV type O inactivated virus, BTV type 4 inactivated virus, VSV NJ type inactivated virus, BVDV reference strain Oregon CV24 strain (BVDV-1 type), IBRV virus.
[0146] 2. Using the cDNA obtained in step 1 as a template, GeXP multiplex PCR was carried out using the primer combination in Example 1.
[0147] Multiplex PCR reaction system (20 μL): template 1 μL (about 100 ng), Genome Lab GeXP StarterKit 5×buffer 4 μL (the buffer contains universal primers, and the universal primers are primer A shown in sequence 16 of the sequence listing and sequence 17 of the sequence listing The composition of primer B shown, wherein the 5' end of primer A is labeled with CY5 fluorescent group, the working concentration of primer A and primer B are both 0.25μM), MgCl 2 (25 μM) 4 μL, primer mix ...
Embodiment 3
[0162] Example 3, universality
[0163]1. Extract the total RNA of the sample to be tested and reverse transcribe it into cDNA. The samples to be tested are: FMDV type O inactivated virus, FMDV type A inactivated virus, FMDV Asia type I inactivated virus, BTV type 4 inactivated virus, BTV type 8 inactivated virus, BTV type 9 inactivated virus, BTV 15 inactivated virus, BTV 17 inactivated virus, BTV 18 inactivated virus, VSV NJ inactivated virus, VSV IND inactivated virus, BVDV reference strain Oregon CV24 strain (BVDV-1 type), BVDV Reference strain NADL strain (BVDV-1 type), BVDV reference strain Yak strain (BVDV-1 type), BVDV strain GX-BVDV1, BVDV strain GX-BVDV2, BVDV strain GX-BVDV3, BVDV strain GX -BVDV4, BVDV strain GX-BVDV5, BVDV strain GX-BVDV6, BVDV strain GX-BVDV7, BVDV strain GX-BVDV8, BVDV strain GX-BVDV9, BVDV strain GX-BVDV10, BVDV strain GX- BVDV11, BVDV strain GX-BVDV12, BVDV strain GX-BVDV13, BVDV strain GX-041, IBRV virus.
[0164] 2. Using the cDNA obtaine...
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