Detection kit, primer and probe capable of simultaneously detecting and identifying foot-and-mouth disease and vesicular stomatitis
A technology for vesicular stomatitis and a kit, which is applied in the field of inspection and quarantine, can solve the problems of limited application, difficult determination of results, low sensitivity, etc., to ensure specificity and exclusivity, saving detection time and cost, coverage and universality Good results
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Embodiment 1
[0038] Composition and use of embodiment 1 test kit
[0039] 1. The composition of the kit
[0040] Table 2 Composition of the kit
[0041]
[0042]
[0043] Among them, 2×Multiplex RT-PCR buffer and Multiplex enzymes were purchased from Path-ID TMMultiplex one-step RT-PCR kit from AB Company.
[0044] The primer mix includes 2 forward primers, 3 reverse primers for FMDV, 2 forward primers, 1 reverse primer for VSV-NJ, 1 forward primer and 1 reverse primer for VSV-IND, primers The sequence is shown in Table 1. The working concentration of the mixed primers is 400nM, and the primers are synthesized by Dalian Bao Biology Co., Ltd.
[0045]The FMDV probe mixture includes 2 probes for FMDV, 1 probe for VSV-NJ and 1 probe for VSV-IND. The probe sequences are shown in Table 1, and the concentrations are 200nM. The probes were synthesized by Dalian Bao Biology Co., Ltd.
[0046] The negative control is sterile water without nucleic acid.
[0047] FMDV positive control is in...
Embodiment 2
[0092] Embodiment 2, the sensitivity test of kit
[0093] 1. Materials
[0094] Foot-and-mouth disease virus and vesicular stomatitis virus are kept in our laboratory.
[0095] 2. Method
[0096] 1) Preparation of positive standard
[0097] Method as described in Example 1.
[0098] 2) Quantitative determination of standard
[0099] Take the prepared in vitro transcribed cRNA and make 200-fold dilutions with RNase-free sterilized water, and measure its absorbance values at 260 nm and 280 nm (OD 260 and OD 280 ), calculate the concentration and purity of the sample to be tested. Pure RNA: 1.7260 / OD280 2.0 indicates that there may be residual isothiocyanate). Concentration of RNA sample (μg / μL): OD 260 ×Dilution factor×40 / 1000, and calculate the copy number (Copies / μL) according to the following formula:
[0100]
[0101] Standard curve drawing:
[0102] Perform 10-fold gradient dilution of the FMDV in vitro standard and then perform fluorescent RT-PCR. Use the r...
Embodiment 3
[0115] Embodiment 3, the specificity test of kit
[0116] 1 material
[0117] The viruses used in this experiment are listed in Table 6.
[0118] Table 6 Viruses and nucleic acids used in the specificity test research process
[0119] Virus source Foot-and-mouth disease virus (FMDV) The lab saves Vesicular stomatitis virus Indiana type (VSV-IND) The lab saves New Jersey-type vesicular stomatitis virus (VSV-NJ) The lab saves Bovine Enzootic Leukemia Virus (BVDV) The lab saves Pseudorabies virus The lab saves Bluetongue Virus (BTV) The lab saves transmissible gastroenteritis virus (TGEV) The lab saves
[0120] 2. Method
[0121] 2.1 Use the primers and probes of foot-and-mouth disease virus, New Jersey-type vesicular stomatitis virus and Indiana-type foot-and-mouth disease virus to perform fluorescent RT-PCR detection on the other 6 viral nucleic acids in the table to verify the specificity of the primers and pro...
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