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95 results about "Respiratory pathogen" patented technology

A respiratory pathogen is a virus, bacteria, parasite or other agent that has gotten into a patient’s lung, throat, nose or other part of the respiratory system.

System and method for diagnosis of infectious diseases

A biosafe apparatus is disclosed for assay and diagnosis of respiratory pathogens comprising a nasal sampling device, a single entry, disposable microfluidic cartridge for target nucleic acid amplification, and an instrument with on-board assay control platform and target detection means.
Owner:PERKINELMER HEALTH SCIENCES INC

Respiratory tract micro-fluidic chip rapid detection technology and kit

The invention is based on a micro-fluidic chip technology and performs rapid detection on seven respiratory tract pathogenic bacteria in combination with a nucleic acid isothermal amplification technology, and belongs to the field of safe and rapid detection of respiratory tract pathogenic bacteria. According to the technology, a sample subjected to rapid treatment is mixed with a reagent in a kit. The mixed liquid is added into a micro-fluidic chip. A primer pre-loaded into the micro-fluidic chip is subjected to a nucleic acid isothermal amplification reaction with a possible microbial gene template in the mixed liquid at certain single temperature. A fluorescent dye in the reaction system is combined with an amplification product to generate a fluorescent signal. Whether the seven pathogens exist in the respiratory tract or not is determined through instrument reading. According to the method, the need for the sample quantity is reduced through the micro-fluidic chip technology, the detection throughput is increased, and seven pathogenic bacteria can be detected at the same time. By adopting the nucleic acid isothermal amplification technology, the detection specificity and sensitivity are improved; the operation is simple, and the reaction time is short. A simple and rapid respiratory tract pathogenic bacteria detection technology is provided for clinical use.
Owner:BEIJING BAIKANGXIN BIOLOGICAL SCI & TECH

Multi-fluorescent quantitative PCR reagent kit capable of synchronously detecting three bovine respiratory pathogens, and multi-fluorescent quantitative PCR detection method capable of synchronously detecting three bovine respiratory pathogens

The invention belongs to the technical field of livestock disease detection, and discloses a multi-fluorescent quantitative PCR reagent kit capable of synchronously detecting three bovine respiratorypathogens as well as a multi-fluorescent quantitative PCR detection method capable of synchronously detecting the three bovine respiratory pathogens, wherein the three bovine respiratory pathogens arerespectively mycobacterium bovis, mycoplasma bovis and Klebsiella pneumoniae. According to the multi-fluorescent quantitative PCR detection method capable of synchronously detecting the three bovinerespiratory pathogens, 3 groups of specific primers and probes are designed and synthesized on basis of a specific sequence 229bp of the mycobacterium bovis, a uvrC gene of the mycoplasma bovis and aKhe gene of the Klebsiella pneumoniae, thereby establishing the multi-fluorescent quantitative PCR detection method capable of synchronously detecting the mycobacterium bovis, the mycoplasma bovis andthe Klebsiella pneumoniae which are associated with respiratory diseases in cattle. The multi-fluorescent quantitative PCR detection method is capable of synchronously detecting the 3 bacteria; and sensitivity, repeatability and specificity tests have proven that the detection method is high in sensitivity, strong in specificity and relatively good in repeatability.
Owner:CHINA AGRI UNIV

Application of trefoil factor 2 in preparation of medicine for treating and preventing lung/bronchial acute inflammation diseases

The invention belongs to the technical field of biomedicine and relates to an application of TFF2 protein in preparation of a medicine for treating and preventing lung / bronchial acute inflammation diseases. In the invention, the significantly different gene expression of the lung tissues of mice infected by severe flu and mild flu are analyzed and screened by a transcriptome chip, and the screened TFF2 is a protective factor; and according to in-vitro synthesis of TFF2 protein, the survival rate of the flu-infected mice can be remarkably increased by dropwise adding the TFF2 protein while the weight loss of mice is reduced. Further study shows that the TFF2 does not influence the flu virus replication but can reduce the secretion of inflammatory factors, promote the repair of the pulmonary mucosa and reduce the damage of lung tissues. Since the mechanism of other respiratory pathogens or physical and chemical factors causing respiratory tissue damage is similar to that of flu virus infection and the protection of TFF2 on flu virus infection is not specific protection but broad-spectrum protection, the TFF2 plays an important protection role in an acute inflammation damage model induced by respiratory pathogens or other factors.
Owner:SHANDONG RUIYING PIONEER PHARMA

Composition and kit for detecting 23 respiratory pathogens and detection method of kit

The invention relates to a composition for detecting 23 respiratory pathogens. The composition comprises a primer composition consisting of the sequences shown by SEQ ID NO. 1-SEQ ID NO. 48 and a probe composition consisting of the sequences shown by SEQ ID NO. 49-SEQ ID NO. 72. The invention also relates to a kit for detecting 23 respiratory pathogens and a detection method of the kit. The kit comprises a first reaction solution, a second reaction solution, a first hybridization solution and a second hybridization solution containing the primers and probes respectively; the kit also comprises a mixed enzyme, a streptavidin-phycoerythrin solution, a negative reference, a positive reference and an interior label. The kit and the detection method provided by the invention integrate the functions of RT-PCR, full-automatic liquid-phase chip hybridization detection, data analysis and the like, and also have the advantages of high throughput, multiple detection target spots, high degree of automation, easiness in operation, short time consumption among the inventions of the same kind of liquid-phase chip technologies, etc.; moreover, the kit and the detection method provide important information for addressing the respiratory tract infection epidemic in time, and are of great significance to the prevention and control of respiratory pathogens.
Owner:SUZHOU SYM BIO LIFESCI CO LTD

Equine rhinovirus 1 proteins

Equine rhinovirus 1 (ERhV1) is a respiratory pathogen of horses which has an uncertain taxonomic status. The nucleotide sequence of the ERhV1 genome and amino acid sequence have been substantially determined (FIG. 2). The predicted polyprotein was encoded by 6,741 nucleotides and possessed a typical picornavirus proteolytic cleavage pattern, including a leader polypeptide. The genomic structure and predicted amino acid sequence of ERhV1 were more similar to those of foot-and-mouth disease viruses (FMDV), the only members of the aphthovirus genus, than other picornaviruses. Nucleotide sequences coding for the complete polyprotein, the polymerase, and VP1 were analyzed separately. The phylogenetic trees confirmed that ERhV1 was more closely related to aphthoviruses than to other picornaviruses. Virion proteins and virus-like particles are described and probes, primers, antigens, vectors, diagnostics and tests developed.
Owner:UNIVERSITY OF MELBOURNE

Multi-linkage probe amplification identification kit capable of detecting a plurality of avian respiratory pathogens

The invention relates to the field of inspection and quarantine, and aims to provide a multi-linkage probe amplification identification kit capable of detecting a plurality of avian respiratory pathogens. The kit comprises: a pre-amplification primer mixed liquid containing pre-amplification primers with a sequence as shown in SEQ ID NO: 1-14; a probe mixed liquid containing a left probe and a right probe with sequences as shown in SEQ ID NO: 15-28; MLPA buffer solution; ligation buffer solution A; ligation buffer solution B; Ligase-65; PCR reaction mixed liquid containing a universal primer with a sequence as shown in SEQ ID NO: 29 and 30; SALSA polymerase; negative control; and positive control. The kit of the invention has the characteristics of high flux, can simultaneously detect 7 pathogens, and can automatically detect 96 samples at a time by using a fully automatic nucleic acid analyzer, and provides a high-flux detection technology for differential diagnosis and emergency diagnosis of pathogens. In addition, the kit has the advantages of good specificity and high sensitivity, and can detect at least 1 copy of target genes by increasing a RT-PCR step to enrich target genes.
Owner:ZHEJIANG FORESTRY UNIVERSITY

Kit for detecting nucleic acid of respiratory tract pathogen, detection method and application

The invention provides a kit for detecting nucleic acid of respiratory tract pathogens. The kit comprises a CRISPR-Cas detection system: crRNA, Cas protein and a nucleic acid probe as shown in the invention. The invention also provides a detection method of the nucleic acid of the respiratory tract pathogen, a separated nucleic acid, crRNA, a primer pair and application thereof. The kit and the detection method disclosed by the invention do not depend on large instruments, enable the results to be directly observed by naked eyes, can realize detection under mild conditions, and are more convenient in detection; the kit and the detection method provided by the invention can be used for efficiently and quickly detecting / diagnosing respiratory pathogens (such as influenza A, influenza B and novel coronavirus); the kit is high in specificity and sensitivity, and can be used for detecting and screening respiratory pathogens, such as rapidly distinguishing various respiratory pathogens including influenza A, influenza B and novel coronavirus.
Owner:SHANGHAI TECH UNIV

Primer combination capable of identifying enterovirus type 71 and application of primer combination

The invention discloses a primer combination capable of identifying enterovirus type 71 and application of the primer combination. The primer combination disclosed by the invention is composed of 6 types of DNA (Deoxyribonucleic Acid) molecules shown as a sequence 1, a sequence 2, a sequence 3, a sequence 4, a sequence 5 and a sequence 6. The primer combination can be used for identifying or assisting to identify whether a virus to be detected is the enterovirus type 71 or not, can also be used for detecting whether a sample to be detected is infected with the enterovirus type 71 or not. A detection method provided by the invention can be used for successfully detecting the enterovirus type 71 without a non-specific reaction with other common respiratory pathogen microorganisms; the detection method is high in accuracy, high in sensitivity and high in specificity.
Owner:CAPITALBIO CORP

Primer combination for nanopore sequencing library building of respiratory pathogens and application of primer combination

The invention discloses a primer combination for nanopore sequencing library building of respiratory pathogens and an application of the primer combination. The primer combination for library buildingis utilized to carry out the nanopore sequencing library building of the respiratory pathogens. According to the method, the library building purpose can be achieved only through the two steps of PCRamplification and joint connection, and during the PCR amplification in the second step, it is only required to supplement with primers without adding enzymes, so that the operation steps are simple;the characteristic of rapid library building is achieved so that real-time sequencing and analysis can be realized; and meanwhile, a bacterial metagenome and a fungal metagenome in a sample are detected.
Owner:GUANGZHOU DARUI BIOTECH

Fully-premixed freeze-drying multi-fluorescent PCR detection kit for novel coronavirus, influenza A virus and influenza B virus and detection method thereof

The invention discloses a multi-fluorescent PCR rapid detection kit for novel coronavirus, influenza A virus and influenza B virus. The kit comprises freeze-dried solid RT-PCR Mix, liquid redissolution Buffer, freeze-dried solid positive control and freeze-dried solid negative control, wherein the freeze-dried solid RT-PCR Mix contains a primer group corresponding to primer sequences of a SARS-CoV-2 specific gene ORF1ab, an influenza A M gene, an influenza B M gene and a human reference gene RNAse P. The kit combines a multi-fluorescent quantitative PCR technology and a freeze-drying process, utilizes three pairs of special primers and human reference genes to amplify specific sequences of three pathogens in vitro, and performs real-time detection in combination with a fluorescent probe. The detection method is simple and convenient to operate, has low requirements for the operation level of detection personnel, and can detect three common respiratory pathogens at a time, the detection time and the detection cost are greatly saved, rapid screening of large-batch samples is realized, the whole detection process only takes 40 minutes to 1 hours, and results are accurate and reliable.
Owner:青岛巴特菲科技发展有限公司
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