44results about How to "High diagnostic sensitivity" patented technology

Methods and systems are provided for diagnosing each of a plurality of engine cooling system components including various valves and grill shutters. Each valve may be individually closed and opened for a specified duration, and corresponding changes in coolant temperature may be monitored. If all the components are functional, the various valves may be adjusted to stagnate coolant at the engine and expedite engine warm-up during a cold-start.

A device and method of detection and treatment of a solid cancer tumor, for example prostate cancer. In a diagnostic method, ultrasound is used to extract a cancer tumor marker from interstitial fluid into a coupling medium. In a method for treating a solid tumor, ultrasound is used to deliver one or more drugs from the coupling medium directly to the site of the tumor.

An invention relating to therapeutic pharmacological agents and methods to chemically induce intracellular hyperthermia and / or free radicals for the diagnosis and treatment of infections, malignancy and other medical conditions. The invention relates to a process and composition for the diagnosis or killing of cancer cells and inactivation of susceptible bacterial, parasitic, fungal, and viral pathogens by chemically generating heat, and / or free radicals and / or hyperthermia-inducible immunogenic determinants by using mitochondrial uncoupling agents, especially 2,4 dinitrophenol and, their conjugates, either alone or in combination with other drugs, hormones, cytokines and radiation.

A method for diagnosing or differentially diagnosing a cancer characterized by the presence of cancer cells in the pleural fluid of a mammalian subject, the method comprising contacting a sample of pleural fluid of the subject with colloidal magnetic particles coupled to a ligand which binds to a determinant on a cancer cell, but does not bind above a baseline threshold to other cellular and non-cellular components in pleural fluid; subjecting the pleural fluid-magnetic particle mixture to a magnetic field to produce a cell fraction enriched in ligand coupled-magnetic particle-bound cancer cells, if present in the pleural fluid; and analyzing the enriched fraction for the number of cancer cells in the pleural fluid. In certain aspects, this method involves preparing the pleural fluids for the above-noted method steps by, e.g., dilution of unprocessed pleural fluid. In certain aspect, the pleural fluid is subjected to the diagnostic method within 24 hours of withdrawal from the subject. This method has advantages to present diagnostic procedures for identifying malignant pleural effusions. The tumor cells present in pleural fluid can be characterized with cellular and molecular markers to determine prognostic and predictive factors.

Disclosed herein are methods, reagents and apparatus for rapid detection of microorganisms in swab-collected samples collected from testing objects. Testing objects include food surface, and human body sites.

Methods and systems are provided for diagnosing each of a plurality of engine cooling system components including various valves and grill shutters. Each valve may be individually closed and opened for a specified duration, and corresponding changes in coolant temperature may be monitored. If all the components are functional, the various valves may be adjusted to stagnate coolant at the engine and expedite engine warm-up during a cold-start.

The invention discloses a double-fed wind generator rotor winding three-phase asymmetric load fault diagnosis method which includes the steps: 1 building a double-fed wind generator rotor winding fault simulation system on a dynamic simulation experiment platform; 2 acquiring rotor current or voltage signals on a rotor side before and after fault in different running states of a motor, correspondingly recording waves by a fault wave recording analysis device, reading data by a MATLAB (matrix laboratory), filtering direct current components and performing FFT (fast Fourier transform) processing; 3 extracting obviously changed frequency serving as fault diagnosis characteristic frequency before and after fault according to amplitude change to judge whether a double-fed wind generator rotor winding has three-phase asymmetric load faults or not. Diagnosis results are quite approximate to true values and effective, diagnosis accuracy is high, and operability is strong.

The present invention relates to: a composition for detecting a gastric cancer marker comprising a preparation for measuring the expression level or methylation level of mRNA of ADCY3 or a protein thereof; a kit for diagnosing gastric cancer, containing the composition; a method for diagnosing gastric cancer by treating a biological sample with the preparation to ascertain whether a material for complementarily binding to the preparation exists and comparing the amount thereof with a control group; a composition for treating and preventing gastric cancer, containing a preparation capable of inhibiting ADCY3 polynucleotide or ADCY3 polypeptide; and a method for treating gastric cancer by administering the composition to an individual. According to the present invention, it is possible to diagnose gastric cancer with high diagnostic sensitivity and specificity using ADCY3 as a marker for diagnosing gastric cancer, and thus can greatly contribute to reducing mortality due to gastric cancer.

The invention provides isolated, purified, recombinant receptor binding proteins Gp-6, Gp-10 and Gp-31 from mycobacterium phage L5, and methods for producing these recombinant receptor binding proteins. The invention also provides the use of recombinant receptor binding proteins, including Gp-6, Gp-10 and Gp-31, as probes for the identification and diagnosis of mycobacterium infections and conditions caused by mycobacterium. Further provided by the invention are methods of targeting mycobacteria using recombinant receptor binding proteins, including Gp-6, Gp-10 and Gp-31. Other methods provided by the invention include the use of recombinant receptor binding proteins, such as Gp-10, in diagnostic assays for diseases, such as Johne's disease, in animals, including ruminants.

The invention discloses a turbo-generator excitation winding turn-to-turn short circuit fault diagnosis method. The method comprises the following steps: 1) a generator finite element model is established, and a rotor fundamental frequency vibration and a phase angle caused by different excitation winding turn-to-turn short circuit faults are calculated to serve as a sample set of fault diagnosis;and 2) rotor vibration data during operation of the generator is collected online and in real time, the correlation degree between the vibration data and the fault sample set is obtained, and the fault degree and the fault position of the excitation winding turn-to-turn short circuit are obtained. According to the turbo-generator excitation winding turn-to-turn short circuit fault diagnosis method provided by the invention, according to the influence of electromagnetic and heat imbalance caused by the excitation winding turn-to-turn short circuit faults on the vibration of the rotor, the vibration characteristic is extracted, good diagnosis sensitivity is achieved, a new detection device does not need to be installed, thereby improving the fault diagnosis efficiency, and the method has the advantages of being simple and easy to implement and high in reliability.

The invention provides a qPCR method and a reagent for quickly detecting MRSA (Methicillin Resistant Staphylococcus Aureus). The qPCR method comprises the following steps: (1) preliminary preparationprocedure; (2) nucleic acid extraction and purification; (3) primer / probe design, synthesis and labeling; (4) qPCR amplification and result judgment; (5) detection lower limit and amplification linearrange test; (6) gene fragment sensitivity and specificity calculation; (7) diagnostic sensitivity and specificity calculation; (8) a statistical method. The qPCR method and the reagent provided by the invention have the benefits that the detection lower limit is as low as 4cfu / reaction, and the amplification linear range reaches 2.0*10<2-8> Copies / ml; the sensitivity and the specificity of MRSA identification are 100 percent (352 / 352) and are 100 percent (77 / 77) respectively, and the sensitivity and the specificity of MRSA detection are 100 percent (94 / 94) and 95.4 percent (94 / 98) respectively; the qPCR method is simple and convenient, quick, high in sensitivity and good in specificity and not only can improve the diagnostic ability of MRSA infection, but also can realize the quick detection, thereby gaining time for early and accurate treatment.

The invention provides an EB virus BFRF3-BZLF1 fusion protein, a gene, a vector containing the BZLF1 fusion protein, a host cell, a test strip, a production method and application thereof. The EB virus BFRF3-BZLF1 fusion protein is obtained by connecting the EB virus BFRF3 protein or an EB virus BFRF3 protein fragment with an EB virus BZLF1 protein or EB virus BZLF1 protein fragment through a connecting peptide, and preferably, the EB virus BFRF3-BZLF1 fusion protein has an amino acid sequence shown in SEQ ID NO:1. The EB virus BFRF3-BZLF1 fusion protein can be used as a target antigen for detecting an EB virus, provides a basis for screening and early diagnosing nasopharyngeal carcinoma, infectious mononucleosis and Burkitt lymphoma, and has the advantages of simplicity, rapidness, sensitivity and specificity.

The present invention relates to bio-secure means for the detection of pathogens and provides a bio-secure reaction vessel and methods of preparing a sample for PCR-based pathogen detection. The reaction vessel comprises a reaction chamber portion (1); a cap holder portion (2); and a cap (3). Two points of security, such as two O-ring seals (9, 10), are provided between the cap (3) and the reaction chamber portion (1). A first seal (9) may be located at a top of the cap holder portion (2) and a second seal (10) may be located at a base of the cap (10).

The invention discloses a reagent kit for detecting cancer-related DNA methylation and application of the reagent kit for detecting cancer-related DNA methylation. The invention provides the application of the substances for detecting CCGG site methylation levels of RASSF1A gene, OPCML gene and HOXA9 gene in the promoter region of the genome of the sample to be detected in the preparation of products for identifying or assisting identification whether the sample to be detected is a cancer sample. Experiments prove that the method and the promoter of the reagent kit for detecting cancer-related DNA methylation are capable of identifying whether the sample to be tested is a cancer sample or whether the subject to be tested is a cancer patient, so that a single sample can be timely and accurately identified; compared with the detection of methylation status of a single gene, the reagent kit for detecting cancer-related DNA methylation has higher diagnostic sensitivity and better specificity; moreover, the statistic analysis and the cumulative analyses are replaced by threshold values, so that instant diagnosis of cancer can be more likely realized.

The technical problem underlying the present invention is to provide peptides corresponding to immunologically important epitopes on bacterial and viral proteins, as well as the use of said peptides in diagnostic or immunogenic compositions. The invention relates to a process for the in vitro determination of antibodies, wherein the peptides used are biotinylated, particularly in the form of complexes of streptavidin-biotinylated peptides or of avidin-biotinylated peptides.

The invention relates to a hydrothorax fluid metabolite combination, a kit and a method for diagnosing tuberculous pleurisy. The hydrothorax fluid metabolite combination for diagnosing tuberculous pleurisy comprises dimethylglycine, tyrosine, kynurenine, nicotinamide, betaine, acylcarnitine with the ratio of 12: 0, acylcarnitine with the ratio of 14: 2 and phosphatidylcholine with the ratio of 42:8. The kit for diagnosing tuberculous pleurisy comprises an internal standard substance required for detecting the concentrations of dimethylglycine, tyrosine, kynurenine, nicotinamide, betaine, acylcarnitine with the ratio of 12: 0, acylcarnitine with the ratio of 14: 2 and phosphatidylcholine with the ratio of 42: 8 in a pleural effusion sample extraction solution. A combined marker provided bythe invention has the characteristics of high sensitivity and high specificity for the diagnosis of tuberculous pleurisy, meanwhile, can be complementary with the traditional marker adenosine deaminase, and can be used for the auxiliary diagnosis of the tuberculous pleurisy by being combined with the traditional marker adenosine deaminase.

The invention relates to a novel application of small molecule metabolites glucose-6-phosphoric acid, erythritol 4-phosphoric acid, xanthine and phosphatidylcholine PC (33:1) in a tissue sample as a combined metabolic marker in preparation of a kit for diagnosing patients with lung cancer and lung benign nodules in subjects. The invention further relates to a kit for detecting the lung cancer and lung benign nodule patients in subjects. By detecting the relative concentrations of the combined markers in tissue samples of the subjects, the variable P value of the combined markers is calculated on the basis of a binary logistic regression equation, and then based on a determined cut-off value, the patients with lung cancer and lung benign nodules are diagnosed. In addition, the combined marker also has better diagnostic ability for patients with early lung cancer and lung benign nodules. The kit can realize high-sensitivity and high-efficiency detection of several small molecule metabolites involved in the invention, and has the characteristics of low detection cost and good repeatability.

The present invention discloses the use of Mycobacterium tuberculosis antigens for use in in vivodetermination of the presence of Mtbinfection in immunocompromised persons or persons co-infected with HIVand the for preparing a diagnostic reagent for skin testing (a skin test reagent) for robust assessment of the presence of Mtbinfection in an individual wherein the individual is an immunocompromised person or a person co-infected with HIV.

The invention provides a series of polypeptides obtained through screening with a phage display peptide library technology and having a prostate cancer targeting characteristic. The binding polypeptides have high specificity and can be applied to general survey of high risk groups of the prostate cancer, early clinical diagnosis of the prostate cancer and evaluation of a treatment effect.

The invention relates to short-chain polypeptides PCP4 capable of being specifically bound to prostate cancer cells and an application of the short-chain polypeptides PCP4 and provides a series of polypeptides obtained through screening with a phage display peptide library technology and having a prostate cancer targeting characteristic. The binding polypeptides have high specificity and can be applied to general survey of high risk groups of the prostate cancer, early clinical diagnosis of the prostate cancer and evaluation of a treatment effect.

The invention discloses a kit for detecting or assisting in detecting ethambutol resistance of multiple drugs resistant bacillus tuberculosis. The kit comprises a product for detecting an embB354 mutation site in an embB gene, wherein the nucleotide sequence of the embB gene is the sequence 1 shown in a sequence table; and the embB354 mutation site is that nucleotide GAC from the 1060th site to the 1062nd site at the 1-5' ends of the sequences in the sequence table is mutated into GCC. Tests show that the new mutation site embB354 of the embB gene can be used for detecting the ethambutol resistance of the multiple drugs resistant bacillus tuberculosis, and the mutation site embB354 is combined with another three mutation sites, namely, embB306, embB406 and embB497, to detect the ethambutol resistance of the multiple drugs resistant bacillus tuberculosis together so as to ensure higher diagnosis sensitivity.

The present invention relates to methods of screening biological samples for the presence of Strongyloides spp. More particularly, the present invention relates to a sensitive and specific screening test for the presence of anti-Strongyloides spp antibodies, protein or nucleic acid in subjects using particular Strongyloides spp L3 stage antigens and nucleic acids encoding same which have diagnostic efficacy.