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37 results about "Swine virus" patented technology

Chinese herbal medicinal feed additive for preventing and controlling swine infectious disease

InactiveCN101695342APrevention and treatment of asthmaPrevention and treatment of contagious pleuropneumoniaFood processingAnimal feeding stuffMedicinal herbsBaical Skullcap Root
The invention provides a Chinese herbal medicinal feed additive for preventing and controlling swine infectious disease. The swine feed additive consists of 37 Chinese medicinal herbs, namely, gypsum, rehmannia root, rhinoceros horn, golden thread, cape jasmine fruit, tree peony bark, baical skullcap root, red paeony root, figwort root, common anemarrhena rhizome, forsythia suspensa , platycodon root, liquorice root, common lophatherum herb, amur corktree bark, honeysuckle flower, Chinese pulsatilla root, indigowoad root, heartleaf houttuynia herb, astragalus, szechwon tangshan root, hawkthorn fruit, medicated leaven, barley sprout, radish seed, chicken's gizzard -membrane, Chinese thorowax root, common andrographis herb, philippine violet herb, tuber fleeceflower root, massa medicata fermentata fujianensis, cyrtomium rhizome, tung leaf, tangerine peel, white paeony root, pine needle and indigowoad leaf through scientific compatibility. The feed additive is added into swine feed in the proportion; under the condition of not using any vaccine, the feed additive can effectively prevent and cure severe mixed flu symptoms, infection and other syndromes caused by swine respiratory disease, asthma, contagious pleuropneumonia, swine virus mixed flu, high swine fever, porcine circovirus, swine fever, flu, pseudorabies, salmonellosis, bacillosis, streptococcus, erysipelas, paratyphoid, eperythrozoon, toxoplasm and other multi-pathogeny and provides genuine green food for the market.
Owner:孟祥合

RPA (recombinase polymerase amplification) primer and detection kit for rapidly detecting African swine fever viruses

The invention discloses an RPA (recombinase polymerase amplification) primer and a detection kit for rapidly detecting African swine fever viruses. Target genes can be effectively amplified, specificity is 100%, detection sensitivity is 102 copy / reaction, and sensitivity is equivalent to that of fluorescent quantitative PCR (polymerase chain reaction). Cross reaction between the RPA amplificationprimer and one of classical swine fever viruses, vesicular exanthema swine viruses I, porcine reproductive and respiratory syndrome viruses, porcine circoviruses and the like is omitted. A RPA isothermal amplification system is rapidness in reaction and wide in temperature range, effective amplification of the target genes can be achieved at the temperature of 38-46 DEG C, and the detection kit can rapidly, efficiently and sensitively detect the African swine fever viruses and has the advantages that the kit is simple to operate, high in specificity, safe and free from pollution, reaction results are easily observed and the like. Effective technical means are provided for on-site rapidness detecting and screening of infection nucleic acid of the African swine fever viruses, and the RPA amplification primer has great significance for control of infection spreading of the African swine fever viruses in China and inspection and quarantine in infected areas and entry and exit ports.
Owner:ACAD OF MILITARY SCI PLA CHINA ACAD OF MILITARY MEDICAL SCI INST OF MILITARY VETERINARY MEDICINE

Porcine circovirus type 2 antigen capture ELISA kit

The invention discloses a porcine circovirus type 2 antigen capture ELISA kit. The kit internally comprises an enzyme labeled monoclonal antibody which is secreted by a hybridoma cell strain with the preservation number of CGMCC NO.10205. The invention also discloses a capture ELISA method for rapidly detecting the porcine circovirus type 2 and established by utilizing the monoclonal antibody. A porcine circovirus type 2 polyclonal antibody and a porcine circovirus type 2 cap protein monoclonal antibody respectively act as a capture antibody and a detecting antibody. The method can be used for detecting multiple gene type PCV2 viruses; the detection sensibility is 400 TICD50 / ml; the porcine circovirus type 2 has no crossed reaction with other swine viruses, and the toxic value determination method coincidence rate is 88%. The result shows that the method has the advantages of operation simplicity, good specificity, high sensitiveness, short time consumption and the like, can be used for estimating the toxic value of viruses, and can conveniently and rapidly control the quality of PCV2 inactivated vaccine semi-finished products.
Owner:HARBIN VETERINARY RES INST CHINESE ACADEMY OF AGRI SCI +1

Monoclonal antibody specially bound to TGEV (transmissible gastroenteritis of swine virus), pharmaceutical composition, kit and applications of monoclonal antibody, pharmaceutical composition and kit

The invention provides a monoclonal antibody specially bound to TGEV (transmissible gastroenteritis of swine virus) and a kit prepared from the monoclonal antibody. The TGEV can be determined rapidlyand accurately, and strains can be widely determined. Pharmaceutical composition prepared from the antibody can be used for broad-spectrum prevention and treatment of different TGEVs.
Owner:LUOYANG PULIKE WANTAI BIOTECH

Pig viral infectious disease gene recombined live vaccine using canine II type adenovirus as carrier and preparation process thereof

This invention supplies a series of production techniques of gene recombination live vaccine of swine virus contagion with canine ó� adenovirus as carrier and finished goods. The viral live vectors vaccine takes swine important virus zymad protective antigens gene as object gene, which are chosen from HCV-E1, E2 gene, FMDV-VP1íóVP2íóVP3íóVP4 gene, TGEV-SíóNíóM gene, PEDV-SíóNíóM geneú¼SIV-HAíóNA geneú¼RV-GíóN gene, etc. The produced vaccines contain recombined swine influenza virus HA gene adenovirus carrier live vaccine, swine plague virus E2 gene adenovirus carrier live vaccine and recombination swine AsiaI foot-and-mouth disease virus VPI gene adenovirus carrier live vaccine. Recombination virus has good inheritance stability, and vaccine immunization can induct pig develop differential antiviral neutralization antibody. It has good immune protection effect and has no toxic side effect. The goods are facilitating for preserve and transportú”it has long storage life and simple technics, and it fits for commercial manufacture.
Owner:MILITARY VETERINARY RES INST PLA MILITARY MEDICAL ACAD OF SCI

Anti-African swine fever virus p54 protein monoclonal antibody and preparation method and application thereof

The invention relates to an anti-African swine fever virus p54 protein monoclonal antibody and a preparation method and application thereof. According to the invention, polypeptide capable of simulating conservative p54 protein NTD is designed and synthesized, and the polypeptide is coupled with BSA to serve as immunogen, an anti-ASFVp54 protein monoclonal antibody is prepared by immunizing a BALB / c mouse through an immunological method, the obtained antibody can specifically identify and bind to an N-terminal region of p54 protein, and the recognition region (aa 1-29) is different from the existing commercial monoclonal antibody. The invention provides gene sequences of a heavy chain variable region and a light chain variable region of the antibody. On this basis, the monoclonal antibodyof the invention can be obtained by adopting a conventional genetic engineering method or a protein engineering method. The monoclonal antibody is high in specificity and high in sensitivity, capableof specifically reacting with the ASFV HLJ / 18 virus strain, without reaction with CSFV, PCV2, PRRSV, PEDV, PRV and other swine viruses, thus laying a foundation for the research of ASFV etiology and pathogenesis and the clinical detection research of ASFV pathogens.
Owner:河南中泽生物工程有限公司

Preventive and therapeutic use of polypeptides from African Swine virus as vaccines

InactiveUS7396531B2Effective in prevention and treatment and diagnosisPeptide/protein ingredientsViral antigen ingredientsMedicineImmunodeficiency
The present invention relates to the use of selected polypeptides from African Swine virus for the prevention and therapy of African Swine infections as well as other infections, including immune deficiencies in mammals and humans.
Owner:RATH MATTHIAS +1

Porcine interferon alpha and application thereof

The invention provides a porcine interferon alpha and an application thereof. The porcine interferon alpha is synthesized through selecting high-expression codon design according to the codon bias of the of a Escherichia coli prokaryotic expression system, the amino acid sequence of the porcine interferon alpha is represented by SEQ ID NO. 1, and the nucleotide sequence for encoding the porcine interferon alpha is represented by SEQ ID NO. 2. A method for preparing the porcine interferon alpha has the advantages of simplicity, low cost, easiness in industrial production, high expression level of the porcine interferon alpha, thorough denaturation in the inclusion body treatment process, and high protein renaturation rate porcine. The porcine interferon alpha prepared in the invention has high titer, can inhibit 100TCID50 vesicular stomatitis virus, has a specific activity reaching up to 10<8>, has good bioactive functions, can be used to prepare medicines for preventing and treating the swine virus infection and enhancing the immune function, and has a broad market application prospect.
Owner:SOUTH CHINA AGRI UNIV +1

Dual fluorescent microsphere immunological detection method for pseudorabies virus gE and gB IgG antibodies

The invention discloses a dual fluorescent microsphere immunological detection method for pseudorabies virus gE and gB IgG antibodies. The detection method is based on a liquid protein chip technology-based carboxylated fluorescent microsphere group for detecting pseudorabies virus antibodies; the group comprises carboxylated fluorescent microspheres coupled with gE truncated proteins and gB truncated proteins, respectively; and the amino acid sequences of gE and gB truncated proteins are shown in SEQ ID NOs: 2 and 4, respectively. The dual fluorescent microsphere immunological detection method for simultaneously detecting PRV gE and gB IgG antibodies is good in reproducibility, high in sensitivity and good in specificity, and has no cross-reaction with other common porcine virus-positiveserums. The method can be used for the rapid differential diagnosis of pseudorabies virus wild-type infected pigs and vaccine-vaccinated pigs and the detection of protective antibodies, thereby providing an important method for the monitoring of swine virus diseases, having a great application value and being worthy of large-scale promotion.
Owner:SOUTH CHINA AGRI UNIV

PR-PCR (Reverse Transcription-Polymerase Chain Reaction) detection kit and detection method of swine transmissible gastroenteritis virus

The invention discloses a PR-PCR (Reverse Transcription-Polymerase Chain Reaction) detection kit of swine transmissible gastroenteritis virus, which comprises an RT reaction solution, a positive control, a negative control, DEPC (diethylpyrocarbonate) water, 2*Taq PCR Master Mix and a primer mixed solution. Compared with an existing detection technology, the PR-PCR detection kit of the swine transmissible gastroenteritis virus has the advantages of high sensitivity, good specificity, simple and practical and the like, and can be used for rapidly detecting transmissible gastroenteritis of swine virus in various clinical samples on a large scale.
Owner:BEIJING DAWEIJIA BIOTECH SHARE CO LTD +1

Recombinant bacillus subtilis for expressing S protein of transmissible gastroenteritis of swine virus

The invention relates to recombinant bacillus subtilis for expressing S protein of transmissible gastroenteritis of swine virus (TGEV), and belongs to the fields of biotechnology and genetic engineering. According to the recombinant bacillus subtilis disclosed by the invention, a TGEV S protein recombinant bacillus subtilis integrated expression plasmid pIncotGSR is successfully constructed, and the expression plasmid is successfully transformed into bacillus subtilis WB800 through electric shock. Based upon Western-blot verification, the TGEV S protein can be successfully expressed in the recombinant bacillus subtilis. An effective TGEV specific immune response level can effectively generate in the body of a one-month-old piglet through stimulation of oral immunization. The recombinant bacillus subtilis is expected to be developed as a genetic engineering oral vaccine for preventing transmissible gastroenteritis of swine.
Owner:NANJING AGRICULTURAL UNIVERSITY

Medicine composition capable of preventing Africa swine fever, extractive thereof, injection and application

The invention provides a medicine composition capable of preventing Africa swine fever, an extractive thereof, an injection and application. The medicine composition is prepared from, by weight, 10-30parts of lucid ganoderma, 4-12 parts of Drosera burmanii, 4-12 parts of Harrisonia perforata, 30-50 parts of areca nuts, 4-12 parts of Callicarpa nudiflora, 4-12 parts of epigeal srephaia roots and 4-12 parts of common nepenthes. The medicine composition has the efficient prevention effect on Africa swine fever, can be widely applied to preventing Africa swine virus, and solves the major problemof the pork industry.
Owner:HAINAN JINZHU AGRI DEV CO LTD

A kind of kit and method for detecting porcine boca virus

The invention belongs to the field of virus diagnosis and detection, solves the technical problems of complicated and long time for detecting porcine boca virus in the prior art, and provides a kit for detecting porcine boca virus, which contains a fluorescent PCR reaction solution, The fluorescent PCR reaction solution contains specific primers, and the sequence of the upstream primer is shown in SEQ ID NO: 1, and the sequence of the downstream primer is shown in SEQ ID NO: 2; it also contains a TaqMan specific probe for porcine boca virus, The sequence of the probe is shown in SEQ ID NO: 3, and it also contains the DNA positive control of the Boca virus plasmid. The present invention also provides a method for detecting porcine Boca virus by using the above-mentioned kit. The kit of the invention can quickly and accurately detect porcine boca virus, has simple operation, short time consumption, high sensitivity and strong specificity, and can qualitatively or quantitatively detect porcine boca virus in various types of specimens.
Owner:SHANGHAI ANIMAL EPIDEMIC PREVENTION & CONTROL CENT

Primer and probe for detecting porcine circovirus type 2 (PCV2), fluorescence quantitative PCR kit, method and application

The invention discloses a primer and a probe for detecting porcine circovirus type 2 (PCV2), a fluorescent quantitative PCR kit, a method and application, wherein the primer has the following nucleotide sequences: the upstream primer is 5'CTACTGCTGTGAGTACCTTGTTGGA 3', the downstream primer is 5'CAGGGTGCTGCTCTGCAA 3'; the sequence of the probe is as follows: 5'FAM-AGCGGGAGTCTGGT-MGB 3'. The invention have the beneficial effects that by adopting the kit disclosed by the invention, PCV2 can be quickly and accurately detected, and the kit has a good linear relationship in the template range of 5.0*10<1> to 5.0*10<9>copies*muL<-1>, has the sensitivity which is 100 times that of conventional PCR, no cross reaction with other swine viruses, and a repeatability test variation coefficient which isless than 1.5%; compared with the conventional PCR method, the method is higher in positive detection rate. In summary, the method has strong specificity, high sensitivity and good repeatability and provides a rapid and accurate detection means for laboratory diagnosis and epidemiological investigation of PCV2.
Owner:SHANDONG NEW HOPE LIUHE GROUP

Application of SVA 3C protein in promotion of porcine virus replication

The invention belongs to the technical field of biology, and experimental research finds for the first time that a protein encoded by an SVA 3C gene can be used as a virus replication enhancer to significantly promote replication of swine viruses including attenuated vaccine strains and inactivated vaccine strains. Therefore, the problems of low virus yield and low vaccine immunogenicity in production and practice at present are well solved. The invention not only provides a new direction for revealing a virus mixed infection mechanism, but also can apply the SVA 3C protein to improve the yield of viruses in production practice, and is more beneficial to optimizing the construction strategies of related genetic engineering live vaccines and live virus vaccine vectors and improving the immune activity of the vector vaccines.
Owner:SOUTH CHINA AGRI UNIV

Primer and kit for simultaneously detecting PEDV, PRRSV, TGEV and PoRV and use method thereof

The invention relates to the technical field of virus detection, and particularly discloses a primer and kit for simultaneously detecting PEDV, PRRSV, TGEV and PoRV and a use method thereof. The PCR detection primer provided by the invention can be used for simultaneously detecting four kinds of viruses including the PEDV, the PRRSV, the TGEV and the PoRV, has no cross amplification reaction withswine fever virus, swine Japanese encephalitis virus, swine Bocavirus, porcine circovirus 2, swine delta circovirus, porcine pseudorabies virus and other swine viruses, and has relatively strong specificity; and the primer is high in sensitivity, the lowest detection concentrations of the primer to the PEDV, the PRRSV, the TGEV and the PoRV are 9.12x10<5> pg / [mu]L, 2.48x10<3> pg / [mu]L, 7.55x10<5>pg / [mu]L and 8.23x10<5> pg / [mu]L respectively, and the detection accuracy is 100%.
Owner:河北三狮生物科技有限公司

Method for screening CTL epitopes from autonomously constructed SLA-2-HB01-pCDH/sT2 cell line

PendingCN114181895AImproved delivery efficiencyConsistent delivery efficiencySkeletal/connective tissue cellsBiological testingCtl epitopeT lymphocyte
The invention belongs to the field of biological medicines, and particularly relates to a method for screening CTL (cytotoxic T lymphocyte) epitopes by an independently constructed SLA-2-HB01-pCDH / sT2 cell line. According to the invention, an exogenous SLA-2-HB01 gene is transfected to an sT2 cell, and a stable SLA-2 gene expression model is established. The method comprises the following steps: loading EB155 and other positive epitope peptides on the surfaces of cells, detecting an SLA-2-peptide-beta2m complex expressed on the surfaces of the cells through FACs, and judging that the SLA-2-HB01-pCDH / sT2 has the function of presenting exogenous polypeptide epitopes. In order to promote the formation of cell surface complexes, the addition of the beta2m is beneficial to the improvement of the presentation efficiency of the antigen polypeptide. In the result of the invention, As63, EB155 and Hu62 peptides can be presented by an SLA-2-HB01-pCDH / sT2 cell line, As63 is presented in the SLA-2-HB01-pCDH / sT2, SLA-2-HB01-Flag-pCDH / sT2 and SLA-2-HB01-3 * Flag-pCDH / in the sT2 cell line, and the presentation efficiency is basically consistent, which indicates that a series of sT2 for expressing the SLA-2-HB01 gene constructed by the invention has the function of presenting the antigen, and the SLA-2-HB01-3 * Flag-pCDH / sT2 can be used for expressing the SLA-2-HB01 gene. Therefore, the SLA-2 heavy chain molecule can be used for screening polypeptide epitopes of the swine viruses on the cellular level, and it is further proved that the antigen presentation function of a cell line is not affected when a Flag tag is added to the C-terminal of the SLA-2 heavy chain molecule.
Owner:DALIAN UNIV

Preparation method for lyophilized agent of swine interferon

The invention discloses a preparation method for a lyophilized agent of swine interferon, belonging to the field of animal vaccines. The preparation method for the lyophilized agent of swine interferon comprises the following six steps: acquiring fresh blood of a healthy pig under aseptic conditions, centrifuging the blood at 4 DEG C for 20 min, sucking up leucocytes at a middle layer, washing the leucocytes with NH4Cl with a mass fraction of 0.85% twice, then carrying out centrifugation, collecting precipitated leucocytes, removing NH4Cl, adding the leucocytes into an Eagle's MEM mixed nutrient solution containing 5% of swine serum according to a volume ratio of the leucocytes to the nutrient solution of 1: 15, carrying out suspension and diluting the swine leucocytes until the number of the swine leucocytes is in a range of 10 * 10<7> / ml to 25 * 10<7> / ml so as to prepare a swine leucocyte suspension liquid; etc. The preparation method is capable of preparing the long-acting swine virus interferon preparation which is injected once every 10 days and has good effect on swine viral diseases.
Owner:宋宏婷

ST IRF3/IRF7 KO cell line and construction method and application thereof

ActiveCN113717943AReduce poison priceInhibition of growth replicationCompound screeningApoptosis detectionWestern blotViral Vaccine
The invention belongs to the field of molecular biology, and relates to an ST IRF3 / IRF7KO cell line and a construction method and application thereof. Specific sgRNA is designed for exons of porcine IRF3 and IRF7 gene sequences and inserted into a vector lentiCRISPR v2, and lentiviral vectors lentiCRISPR v2-IRF3 and lentiCRISPR v2-IRF7 are obtained. After HEK293T cells are transfected by the recombinant plasmids, lentivirus infected ST cells are collected. Successfully infected cells are screened out through antibiotics, sequencing is carried out, and Western Blot verification is carried out. The ST IRF3 / IRF7KO cell line disclosed by the invention can be applied to basic and application research of swine viruses, and a valuable new material is provided for selection of cell lines in production of viral vaccines.
Owner:YANGZHOU UNIV

Composition and preparation method thereof, and traditional Chinese medicine preparation and application thereof

The invention relates to a traditional Chinese medicine composition. The traditional Chinese medicine composition comprises 200 to 2000 parts of euphorbiae humifusae herb, 10 to 200 parts of catechu,10 to 100 parts of dark plum, 10 to 200 parts of scorched hawthorn fruit, 20 to 400 parts of Poria cocos, 10 to 200 parts of white peony roots and 10 to 100 parts of licorice roots. The invention alsorelates to a preparation method for the traditional Chinese medicine composition. The invention further relates to a traditional Chinese medicine preparation and application of the same as a drug fortreating pathogenic diarrhea, nonpathogenic diarrhea, damp-heat type diarrhea or spleen-deficiency type diarrhea caused by swine viruses and bacteria.
Owner:LUOYANG HUIZHONG ANIMAL MEDICINE

A grinding processing device for porcine virus samples

The invention belongs to the technical field of sample treatment equipment. The grinding effect of a traditional porcine virus sample grinding treatment device is poor. Aiming at the problems in the prior art, the invention discloses a grinding treatment device of a porcine virus sample; the grinding treatment device comprises a containing groove, a plurality of arc-shaped rods, a round block, a rotary shaft, a spindle block, a tooth ring, a plurality of grinding wheel gears and an arc-shaped friction block; an annular sliding rail is arranged at the top of the containing groove and filteringholes are formed in the bottom of the containing groove; the upper end of each arc-shaped rod is connected to the round block and the lower end of each arc-shaped rod is connected to a sliding block on the annular sliding rail; the upper end of the rotary shaft is connected to the round block and the lower end of the rotary shaft is connected to a motor; the tooth ring is connected to the rotary shaft; each grinding wheel gear is engaged with the tooth ring; the spindle block comprises a large cone frustum; an arc-shaped surface of the large cone frustum is hinged with a plurality of grindingwheels which are uniformly distributed along the peripheral direction of the arc-shaped surface; each grinding wheel is driven through the corresponding grinding wheel gear to rotate; surfaces of theadjacent grinding wheels are fitted mutually; and the arc-shaped friction block is driven through the arc-shaped rods to rotate and an inner side face of the arc-shaped friction block is fitted to thegrinding wheels. The grinding treatment device of the porcine virus sample disclosed by the invention has a good grinding effect.
Owner:SHANGHAI JIAOTONG UNIV

Chinese herbal medicinal feed additive for preventing and controlling swine infectious disease

InactiveCN101695342BPrevention and treatment of asthmaPrevention and treatment of contagious pleuropneumoniaFood processingAnimal feeding stuffMedicinal herbsHouttuynia
The invention provides a Chinese herbal medicinal feed additive for preventing and controlling swine infectious disease. The swine feed additive consists of 37 Chinese medicinal herbs, namely, gypsum, rehmannia root, rhinoceros horn, golden thread, cape jasmine fruit, tree peony bark, baical skullcap root, red paeony root, figwort root, common anemarrhena rhizome, forsythia suspensa , platycodon root, liquorice root, common lophatherum herb, amur corktree bark, honeysuckle flower, Chinese pulsatilla root, indigowoad root, heartleaf houttuynia herb, astragalus, szechwon tangshan root, hawkthorn fruit, medicated leaven, barley sprout, radish seed, chicken's gizzard -membrane, Chinese thorowax root, common andrographis herb, philippine violet herb, tuber fleeceflower root, massa medicata fermentata fujianensis, cyrtomium rhizome, tung leaf, tangerine peel, white paeony root, pine needle and indigowoad leaf through scientific compatibility. The feed additive is added into swine feed in the proportion; under the condition of not using any vaccine, the feed additive can effectively prevent and cure severe mixed flu symptoms, infection and other syndromes caused by swine respiratory disease, asthma, contagious pleuropneumonia, swine virus mixed flu, high swine fever, porcine circovirus, swine fever, flu, pseudorabies, salmonellosis, bacillosis, streptococcus, erysipelas, paratyphoid,eperythrozoon, toxoplasm and other multi-pathogeny and provides genuine green food for the market.
Owner:孟祥合

A kind of primer combination, probe combination and its application in detecting porcine virus, detection reagent, kit and detection method

The invention discloses a combination of primers, a combination of probes and their application in detecting porcine viruses, a detection reagent, a kit and a detection method; the invention provides a combination of primers, a combination of probes and their application in detecting porcine viruses Application, detection reagents, kits and detection methods, establish a joint detection method for five kinds of porcine viruses, which can quickly detect five major swine diseases of ASFV, FMDV, CSFV, HP‑PRRSV and PRV wild virus, and can achieve high detection of five kinds of viruses Throughput screening improves detection efficiency and reduces reagent consumption, thereby saving costs, shortening detection time, and reducing workload; providing detection reagents that can realize joint detection of five porcine viruses, using optimized primer combinations and probe combinations, so that reagents and The kit using this reagent can specifically and sensitively detect five porcine viruses of ASFV, FMDV, CSFV, HP-PRRSV and PRV wild virus; it can simply and quickly detect five porcine virus infections with different types of nucleic acids in parallel in a single reaction tube, Realized single tube PCR to detect DNA virus and RNA virus at the same time.
Owner:北京市动物疫病预防控制中心

RT-CPA detection primer and kit for swine transmissible gastroenteritis virus

The invention provides an RT-CPA detection primer and kit for swine transmissible gastroenteritis virus, and belongs to the technical field of swine virus disease virus detection, the RT-CPA detection primer comprises SD-CPF, SD-CPR, SD-F, SD-R, SD-DF and SD-DR; and the nucleotide sequences are shown as SEQ ID No.1-6 in sequence. The primer provided by the invention is good in specificity and can effectively detect the swine transmissible gastroenteritis virus; the method is rapid and efficient, the detection time is about 90 min, and the method is very suitable for on-site rapid detection of TGEV; the method does not depend on expensive instruments and equipment and professional detection personnel, and the detection cost is low; the detection result is simple, objective and visual to judge; the sensitivity is high, and 10 copies / mu L of TGEV can be detected.
Owner:GANSU ANIMAL HUSBANDRY & VETERINARY MEDICINE INST
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