35results about How to "Specific detection method" patented technology

The invention relates to a detecting method and medium of bacillus coagulans. The medium includes 5.0-10.0 parts by weight of tryptone, 2.0-3.0 parts by weight of yeast extract powder / extract, 1.0-5.0parts by weight of glucose, 1.0-2.0 parts by weight of polysorbate-80, 0.1-0.5 part by weight of L-cysteine, 0.04-0.06 part by weight of bromocresol purple, and 15.0-20.0 parts by weight of agar. Themedium allows colonies to grow well, and is low in cost and simple and convenient to prepare. A counting result is accurate and reliable when the medium is utilized for detection of the bacillus coagulans.

The invention provides an enropin label idioldast viral infection early stage quotation which is formed by a box 1, a uterus plate 2, a pad 3, an enropin label antibody 4, a negative nature control object 6, a dilution buffer liquid 7, a reacting buffer liquid 8, a washing buffer liquid 9, a reinforcing liquid 10, and an operating instruction 11.

The present invention belongs to the technical field of biology and discloses a LAMP primer combination, detection method and kit capable of distinguishing porcine circovirus type 2 and type 3 typingdetection. The primer combination can respectively detect the porcine circovirus type 2 and the porcine circovirus type 3, and also has no cross reactions with other porcine viruses (such as circovirus type 1, porcine parvovirus, pseudorabies virus, porcine cholera virus, swine influenza virus, highly pathogenic porcine reproductive and respiratory syndrome virus, etc.). Fluorescent dye is added into a LAMP reaction system, so that detection of the porcine circovirus type 2 and / or type 3 can be realized by a one-step method, whole-process real-time monitoring is realized by combining fluorescence quantification, results can be obtained within 1 hour, and detection sensitivity can reach 100 copies / [mu]L. The detection method has advantages of simplicity, convenience, rapidness, sensitivityand specificity, and also avoids errors caused by artificial judgment and environmental pollution caused by uncovering.

The invention relates to a drug resistance detection method for vibrio parahaemolyticus fluoroquinolone medicines. The method comprises the following steps: (1) collecting 1.0-1.2g of live bacteria ofvibrio parahaemolyticus, performing resuspension by using 7-8mL of deionized water, performing repeated freezing and thawing to break cells, performing centrifugation, and collecting supernate so asto obtain a template; (2) commixing the template with fluoroquinolone medicine resistant gene detection primers GyrA-F, GyrA-R, GyrB-F, GyrB-R, ParE-F and ParE-R, and performing PCR (polymerase chainreaction) amplification; and (3) after PCR amplification is completed in the step (2), performing agarose gel electrophoresis and sequencing. The detection method provided by the invention is sensitive, specific and rapid, a very trace amount of target genes can be detected, and tedious vibrio parahaemolyticus culture is not needed.

The invention discloses a fluorescence RT-PCR primer, a probe and a kit for detecting Schmallenberg viruses. The sequences of the primer and the probe are shown as SEQ ID NO. 1-6. The kit comprises the primer, the probe, reverse transcriptase, DNA polymerase, an RNA extraction reagent, a fluorescence PCR reaction reagent, a Schmallenberg virus positive control and a Schmallenberg virus negative control. The Schmallenberg virus fluorescence RT-PCR kit and a detection method provided by the invention are specific, sensitive and quick, have good repeatability and low costs, and the detection method is a favorable method for quickly detecting Schmallenberg viruses.

The invention discloses a real-time fluorescence RT-HDA (Reverse Transcriptase-Helicase-Dependent Isothermal Amplification) kit and a primer for detecting avian influenza virus. A group of primers for detecting the avian influenza virus have an oligonucleotides sequence shown by a sequence table SEQ ID No:1 and a sequence table SEQ ID No:2. The kit and the primer have the following advantages that the novel HDA technology is applied to the detection of the avian influenza virus, and compared with the existing AIV (Avian Influenza Virus) detecting method, the HDA detecting method has the advantages of fastness, more convenience, safety and reliability; for the conventional virus separation and serology method, long time is consumed, the bio-safety risk exists; for the HDA method, a natural reproduction mechanism in a body is simulated, the safety is high, the reaction speed is quick, and the detection can be completed by only 2h at most; and compared with fluorescence PCR (Polymerase Chain Reaction), the HDA detecting method has the advantages that the program setting is easier, the reaction conditions such as annealing temperature and the like do not need to be explored, and the HDA detecting method is easier to master and operate in the aspect of technical level. Due to the optimization of reaction conditions, according to the real-time fluorescence RT-HDA method, at least 10copies / reaction of viral nucleic acid can be detected. The technology has a great application prospect in the monitoring and diagnosis of the avian influenza virus, and the kit and the primer are diagnosis tools with good promotion and application values.

The invention belongs to the technical field of biology and discloses a typing detection LAMP primer combination with an effect of differentiating porcine parvovirus type 1-7, a detection method and akit. Multiple sets of LAMP primers are designed respectively by utilizing conserved segments of the NS1 gene and NP2 gene of a porcine parvovirus and are screened to obtain the typing detection primer combination which has good specificity and high sensitivity and can be used for differentiating the porcine parvovirus type 1-7. The primer combination can be used for respectively detecting porcineparvovirus type 1-7 and does not have a cross reaction with other porcine viruses. A fluorescent dye is added into a LAMP reaction system, the porcine parvovirus type 1-7 can be detected by a one-step method, whole-process real-time monitoring can be implemented by combining fluorescent quantitation, a result can be obtained within 1 hour, and the detection sensitivity can be 100 copies / [mu]L. The detection method has the advantages of convenience, quickness, sensitiveness and specificity and can avoid an error caused by human determination and environmental pollution caused by cap opening.

The invention discloses an RT-HDA kit for detecting avian influenza virus and a primer. The primer for detecting the avian influenza virus is oligonucleotides sequences shown in a sequence table SEQ ID (Sequence ID) NO: 1 and a sequence table SEQ ID NO:2. According to the RT-HDA kit, a novel constant-temperature amplifying technology HDA is used for detecting the avian influenza virus for the first time; compared with a conventional detection method of AIV (Avian Influenza Virus), the RT-HAD kit has the advantages that: (1) an HDA detection method is faster, more convenient, safer and more reliable. A conventional method of separating virus and a conventional serology method need more time, and bring a risk to safety of an organism; the HDA method simulates a natural replication mechanism in vivo, so that the safety is high, a reaction is fast to carry out, and detection can be accomplished by only two hours; and (2) compared with a PCR (Polymerase Chain Reaction), the HDA detection method has the advantages that PCR instruments are saved, a requirement on equipment is simple, only one water bath kettle is needed, so that the technology is convenient to master and operate, the detection method can be convenient to popularize and use in regions with insufficient conditions, and benefits are provided for diagnosing and monitoring the avian influenza virus.

The invention discloses a real-time fluorescence PCR (polymerase chain reaction) kit and an oligonucleotide sequence for detecting swine dysentery. The oligonucleotide sequence for detecting swine dysentery is an oligonucleotide sequence shown from SEQ ID No.1 to SEQ ID No.3 in a sequence table. The invention also provides a detection kit containing the oligonucleotide sequence. The kit and the oligonucleotide sequence have the advantages that: when the real-time PCR technology is applied to swine dysentery detection, the detection specificity and sensitivity are further improved, the workload is reduced, the working efficiency is improved, and a target fragment can be quantitatively detected. By virtue of optimization of reaction conditions, the real-time PCR can detect pathogen amount of 10<2> copy / reaction minimally. 318 clinical samples from 7 pig farms are detected by using the method, and experiment results prove that: the method is a specific, sensitive and efficient detection method. The technology has great application prospect in import and export sample quarantine, as well as monitor and diagnosis of clinical plague.

The invention discloses a real-time fluorescence PCR (polymerase chain reaction) kit and an oligonucleotide sequence for detecting swine dysentery. The oligonucleotide sequence for detecting swine dysentery is an oligonucleotide sequence shown from SEQ ID No.1 to SEQ ID No.3 in a sequence table. The invention also provides a detection kit containing the oligonucleotide sequence. The kit and the oligonucleotide sequence have the advantages that: when the real-time PCR technology is applied to swine dysentery detection, the detection specificity and sensitivity are further improved, the workload is reduced, the working efficiency is improved, and a target fragment can be quantitatively detected. By virtue of optimization of reaction conditions, the real-time PCR can detect pathogen amount of 10<2> copy / reaction minimally. 318 clinical samples from 7 pig farms are detected by using the method, and experiment results prove that: the method is a specific, sensitive and efficient detection method. The technology has great application prospect in import and export sample quarantine, as well as monitor and diagnosis of clinical plague.

The invention discloses a fluorescent PCR detection reagent for identifying cattle gene source in heparin, a preparation method and application, provides a detection method for detecting cattle composition source in a heparin crude finished product, a real-time fluorescence quantification PCR primer and a probe by performing sequencing and comparison on cattle gene, and the length of an amplification target fragment for cattle composition detection is 92 bp. The invention also provides a kit for performing quantitative determination on cattle gene. The detection method and the detection kit have the advantages of accurate detection, high sensitivity, strong specificity and the like, and have good specimen detection capability.

The invention belongs to the field of biotechnology, specifically relates to a monoclonal antibody against riemerella anatipestifer (RA). The preservation number of the monoclonal antibody 5G7 is CGMCC No. 5165. With adopting the monoclonal antibody to prepare the immune colloidal gold strip for detecting the RA, the pathogen of the RA can be directly detected, and the RA strains such as serotypes of 1, 2, 3 and 11 can be synchronously detected, such that the monoclonal antibody against the RA has a wide application value.

The invention discloses a primer pair for preparing a kit for detecting type-4 avian adenovirus and an application thereof. The primer pair comprises an upstream primer and a downstream primer, wherein the nucleotide sequence of the upstream primer is shown by SEQ ID No.1; and the nucleotide sequence of the downstream primer is shown by SEQ ID No.2. The invention also discloses a kit comprising the primer pair and a method for detecting the type-4 avian adenovirus. The primer pair can specifically amplify the Hexon gene segment of the type-4 avian adenovirus in a sample, the detection sensitivity is high, the lowest detection limit reaches 7.2*10<4>ng / mu L, the result is accurate, and the primer pair can be applied to the detection and identification of the type-4 avian adenovirus; the primer pair is universal in detecting different strains of the type-4 avian adenovirus; and the rapid, specific and accurate detection method of the type-4 avian adenovirus provides a detection tool for detecting and controlling the prevalence of the disease.

The invention discloses an RT-HDA (Reverse Transcription-Helicase-Dependent Isothermal Amplification) kit and primers for detecting a foot-and-mouth disease virus. The s for detecting a foot-and-mouth disease virus are oligonucleotide sequences shown in the sequence list SEQ ID No:1 and the sequence table SEQ ID No:2. In the invention, the novel isothermal amplification technology HDA is applied to the detection of the foot-and-mouth disease virus for the first time. Compared with the traditional FDMV detection method, the HDA detection method is quicker, more convenient, safer and more reliable. The traditional virus isolation and serological method has long time consumption and biosafety risk. The HDA method imitates the natural replication mechanism in the body and has high safety and quick response, and only 2 h are needed at most to complete detection. Compared with PCR (Polymerase Chain Reaction), the HDA method does not need any PCR instrument, the equipment requirement is simple, only one water bath kettle is needed, and the HDA method is easier to master and operate speaking from the technology level, is easier to be popularized and applied to regions with insufficient conditions and is more conducive to the diagnosis and monitoring of the foot-and-mouth disease virus.

The invention discloses a pythium splendens braun fluorescence quantitative PCR detection reagent, a detection kit and an application; the detection reagent comprises a pair of specific primers with sequences as shown in SEQ ID NO: 1 and SEQ ID NO: 2, and a specific fluorescence probe with a sequence as shown in SEQ ID NO: 3; an amplification target fragment has a length of 94 bp, and the nucleotide sequence of the amplification target fragment is shown in SEQ ID NO: 4; the detection kit comprises components of a CTAB extract, a PCR buffer containing the primers and the probe, TaqDNA polymerase, positive control liquid, and quantitative standard liquid; the detection method comprises the extraction of total RNA and the fluorescence PCR reaction; detection performed by using the pythium splendens braun fluorescence quantitative PCR detection reagent overcomes disadvantages of time consumption, easy pollution, and electrophoresis detection necessity after amplification of routine PCR, can realize rapid and accurate qualitative and quantitative detection of pythium splendens braun in a sample, and has the advantages of simplicity, easy operations, intuitive results, high sensitivity, good repeatability, and the like.

The invention discloses a primer for discriminating schistosoma japonicas, a corresponding kit and a detection method thereof. The sequence of an upstream primer for discriminating the schistosoma japonicas is shown as SEQIDNO:1, and the sequence of a downstream primer is shown as SEQIDNO:2. In the invention, a method for fast detecting the schistosoma japonica is also established, and the schistosoma japonicas with different types can be discriminated accurately. The primer disclosed by the invention is prepared into the kit, has the advantages that the operating procedure is simplified, the detecting specificity is strong, the sensitivity is high and the result judgment is objective and the like and is suitable for being promoted and applied.

The invention discloses a PCR (Polymerase Chain Reaction) kit and primers for detecting swine dysentery. A group of primers for detecting the swine dysentery have the nucleotide sequences disclosed in a sequence table SEQIDNo: 1 and a sequence table SEQIDNo: 2. The invention has the advantages that compared with etiology separation culture, the PCR technology applied in the detection of the swinedysentery is faster and more convenient, the bacterium separation culture method at least needs 10 days and hard culture conditions, strict anaerobic culture is needed, and the PCR can be completed only in 5 hours; and compared with etiology separation, the PCR needs relatively simple equipment, is more convenient to master and operate from a technical perspective, is more convenient to apply andpopularize in areas with insufficient conditions and is more conductive to the diagnosis and monitoring of the swine dysentery.

The invention discloses a real-time fluorescence RT-HDA (Reverse Transcriptase-Helicase-Dependent Isothermal Amplification) kit and primer for detecting foot-and-mouth disease virus. A group of primers for detecting the foot-and-mouth disease virus have an oligonucleotides sequence shown by a sequence table SEQ ID No:1 and a sequence table SEQ ID No:2. The kit and the primer have the following advantages that the novel HAD technology is applied to the detection of the foot-and-mouth disease virus, and compared with the existing FMDV (Foot-And-Mouth Disease Virus) detecting method, the HDA detecting method has the advantages of fastness, more convenience, safety and reliability; for the conventional virus separation and serology method, long time is consumed, the bio-safety risk exists; for the HDA method, a natural reproduction mechanism in a body is simulated, the safety is high, the reaction speed is quick, and the detection can be completed by only 2 hours at most; and compared with fluorescence PCR (Polymerase Chain Reaction), the HDA detecting method has the advantages that the program setting is easier, the reaction conditions such as annealing temperature and the like do not need to be explored, and the HDA detecting method is easier to master and operate in the aspect of technical level. Due to the optimization of reaction conditions, according to the real-time fluorescence RT-HDA method, at least 10copies / reaction of viral nucleic acid can be detected. The technology has a great application prospect in the monitoring and diagnosis of the foot-and-mouth disease virus, and the kit and the primer are diagnosis tools with good promotion and application values.

The invention relates to a detection method and culture medium for bacillus coagulans. The medium includes: 5.0-10.0 parts by weight of tryptone, 2.0-3.0 parts by weight of yeast extract powder / paste, 1.0-5.0 parts by weight of glucose, 1.0-2.0 parts by weight of polysorbate-80, and 0.1-3.0 parts by weight of L-cysteine 0.5 parts by weight, 0.04-0.06 parts by weight of bromocresol violet, and 15.0-20.0 parts by weight of agar. The culture medium can make the colony grow well, the cost is low, the preparation is simple and convenient, and the counting result is accurate and credible when the culture medium is used to detect the bacillus coagulans.