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24 results about "Hybridization probe" patented technology

In molecular biology, a hybridization probe is a fragment of DNA or RNA of variable length (usually 100–10000 bases long) which can be radioactively or fluorescently labeled. It can then be used in DNA or RNA samples to detect the presence of nucleotide substances (the RNA target) that are complementary to the sequence in the probe. The probe thereby hybridizes to single-stranded nucleic acid (DNA or RNA) whose base sequence allows probe–target base pairing due to complementarity between the probe and target. The labeled probe is first denatured (by heating or under alkaline conditions such as exposure to sodium hydroxide) into single stranded DNA (ssDNA) and then hybridized to the target ssDNA (Southern blotting) or RNA (northern blotting) immobilized on a membrane or in situ. To detect hybridization of the probe to its target sequence, the probe is tagged (or "labeled") with a molecular marker of either radioactive or (more recently) fluorescent molecules; commonly used markers are ³²P (a radioactive isotope of phosphorus incorporated into the phosphodiester bond in the probe DNA) or digoxigenin, which is a non-radioactive, antibody-based marker. DNA sequences or RNA transcripts that have moderate to high sequence similarity to the probe are then detected by visualizing the hybridized probe via autoradiography or other imaging techniques. Normally, either X-ray pictures are taken of the filter, or the filter is placed under UV light. Detection of sequences with moderate or high similarity depends on how stringent the hybridization conditions were applied—high stringency, such as high hybridization temperature and low salt in hybridization buffers, permits only hybridization between nucleic acid sequences that are highly similar, whereas low stringency, such as lower temperature and high salt, allows hybridization when the sequences are less similar. Hybridization probes used in DNA microarrays refer to DNA covalently attached to an inert surface, such as coated glass slides or gene chips, to which a mobile cDNA target is hybridized.

Liquid phase hybridization probe pool, kit and joint detection method for joint detection of multiple pathogens and drug-resistant genes

The invention discloses a liquid-phase hybridization probe pool for joint detection of multiple pathogens and drug-resistant genes. The liquid-phase hybridization probe pool is designed according to target areas of target pathogens and drug-resistant genes; the probe is a probe with unequal length of 30 to 100 nt; comprising a target specific sequence complementarily paired with a target region and a conjugate sequence complementarily paired between adjacent probes; the 5'terminal and the 3 'terminal of the probe are respectively modified with a conjugate sequence A and a conjugate sequence B, so that the adjacent probes can be specifically combined through terminal pairing; the conjugate sequence A is as shown in SEQ ID No. 601, and the conjugate sequence B is as shown in SEQ ID No. 602. According to the method, the constructed library and the specific probe pool are hybridized, so that the capture time is shortened to 30 minutes, and the method is obviously superior to a traditional method. Through optimization, the operation time and complexity are reduced, personal errors are reduced, meanwhile, high sensitivity and specificity are kept, target nucleic acid in a complex sample can be efficiently captured, a high-quality template is provided for subsequent sequencing, and combined detection of multiple respiratory pathogens and drug-resistant genes is supported.
Owner:BEIJING YOUAN HOSPITAL CAPITAL MEDICAL UNIV

Methods, compositions and systems for protein detection

The present disclosure relates to proteomics, including the detection of immune cell target proteins as examples that the disclosed methods can be used for protein detection. Methods, compositions, and systems are described for identifying the presence of proteins, including detecting immune cell proteins from a sample using a combination of multiplex immuno-PCR with antibodies conjugated to oligonucleotides comprising an antibody-specific barcode flanked by PCR priming sites; detection of barcoded amplicons obtained from immuno-PCR with encoded padlock probes comprising codes specific for the barcodes / target protein; rolling circle amplification (RCA) of the circularized padlock probes; and determination of the sequence of the codes amplified by RCA by next generation sequencing or using fluorescently labeled hybridization probes.
Owner:PLENO INC

Fine-adjusted super-specific nucleic acid hybridization probe

The present disclosure relates to finely modulated ultra-specific nucleic acid hybridization probes. The present invention provides compositions and methods for highly specific nucleic acid probes and primers. The probe system includes a complementary strand and a protective strand to partially form a double-stranded probe. The reaction standard free energy ([delta] G DEG rxn = [delta] G DEG t-TC-[delta] G DEG nh-PC + ([delta] G DEG v-TC-[delta] G DEG h-PC)) of hybridization between the probe and the target nucleic acid determined by formula 1 is about-4 kcal / mol to + 4 kcal / mol. Alternatively, the reaction standard free energy of hybridization between the probe and the target nucleic acid determined by Formula 1 is within 5 kcal / mol of the standard free energy determined by Formula 2 (-R [tau] ln (([P] 0-[C] 0) / [C] 0)), the term [P] 0 of Formula 2 being equal to the concentration of the protective strand, and the term [C] 0 of Formula 2 being equal to the concentration of the complementary strand. In addition, the present invention provides a method for the immediate fine modulation of a reaction using the probe of the present invention.
Owner:WILLIAM MARCH RICE UNIVERSITY

Phosphorylation probe capture amplification method

The invention provides a phosphorylated probe capture amplification method. The method comprises the following steps: hybridizing a phosphorylated probe to genome DNA to form a hybridization probe, extending and connecting the hybridization probe to form a closed loop by using a bridging primer to form a closed loop PCR product, and carrying out PCR amplification on the obtained PCR product to obtain an amplified product which is an enriched target area. According to the application, phosphorylation is carried out by taking the probe as a skeleton, a sequence on an Illumina Tru Seq joint and a bridged complementary sequence are added, by adopting a mode of increasing primer bridging, products after probe amplification are connected end to end to form cyclization, and by adopting a mode of increasing EXO1 / EXO3 enzyme digestion, the formation of a dimer is reduced, so that the detection sensitivity is improved, and the detection sensitivity is improved. According to the invention, small-volume hybridization and small-volume amplification modes are adopted, so that the molecular collision probability is increased. The method has ultrahigh specificity and accuracy, each target site is independently amplified, the PCR preference is avoided, the coverage uniformity is superior to that of multiple PCR and hybrid capture, the operation is simple and convenient, the period is short, and the experimental process only needs several hours.
Owner:SHANGHAI HEYIN BIOTECHNOLOGY CO LTD

Fluorescence in-situ hybridization probe group for rapidly distinguishing hexaploid oat chromosomes and application of fluorescence in-situ hybridization probe group

The invention discloses a fluorescence in-situ hybridization probe group for rapidly distinguishing hexaploid oat chromosomes and application thereof, and belongs to the technical field of molecular biology. The fluorescent in-situ hybridization probe group provided by the invention comprises a probe oligo-356 and a probe oligo-898, wherein the nucleotide sequence of the probe oligo-356 is as shown in SEQ ID NO. 1; the nucleotide sequence of the probe oligo-356 is as shown in SEQ ID NO. 2; the provided fluorescence in-situ hybridization probe group can quickly and accurately identify different chromosomes of hexaploid oat through a fluorescence in-situ hybridization method, and has important scientific and practical values for hexaploid oat chromosome structure variation identification, oat genetic relationship identification, oat genetic map construction and oat variety improvement.
Owner:SICHUAN AGRI UNIV

A bone marrow smear FISH test kit and its application

PendingCN122357694AHybridization probeSignal interpretation
This application relates to the field of molecular pathology diagnostic technology, specifically disclosing a bone marrow smear FISH detection kit and its application. The kit includes a rapid hybridization buffer, a stabilization pretreatment solution, room temperature hybridization probes, probe dilution buffer, low-salt washing buffer, high-salt washing buffer, counterstaining solution, positive control samples, and negative control samples. The room temperature hybridization probes include broken probe pairs targeting the BCR-ABL, PML-RARA fusion genes, and IgH gene rearrangements. The detection method of this kit includes sample pretreatment, probe denaturation, room temperature hybridization, washing and counterstaining, and signal interpretation. Through the synergistic effect of the rapid hybridization buffer and the short-chain low-Tm value probes, rapid hybridization at room temperature is achieved, eliminating the need for a dedicated isothermal hybridization instrument. The stabilization pretreatment solution can complete cell permeation and RNA removal in one step, resulting in a high degree of operational standardization.
Owner:SUZHOU YUANDE YOUQIN MEDICAL LAB CO LTD

A marker composition, product and use thereof for lung cancer detection or diagnosis

This invention discloses a biomarker composition, product, and application for lung cancer detection or diagnosis, relating to the field of lung cancer diagnostic technology. The biomarker composition provided by this invention has the advantages of high specificity and high sensitivity; 100% specificity means a zero false positive rate, avoiding unnecessary anxiety, unnecessary radiation exposure, and further invasive examinations. Based on the lung cancer detection or diagnostic biomarker composition provided by this invention, lung cancer diagnostic products, such as reagents, kits, chips, hybridization probes, or sequencing libraries, can be further developed. This will help achieve rapid, highly sensitive, and highly specific detection or diagnosis of lung cancer.
Owner:JIAXING YUNYING MEDICAL INSPECTION CO LTD

Peripheral blood neutrophil molecular typing kit and its application in early diagnosis of lung cancer

This invention relates to a molecular typing kit for peripheral blood neutrophils and its application in the early diagnosis of lung cancer, belonging to the field of oncology technology. The kit comprises a target sequence hybridization probe and a fluorescent reporter probe; the nucleotide sequence of the target sequence hybridization probe is shown in SEQ ID NO: 11-25; the nucleotide sequence of the fluorescent reporter probe is shown in SEQ ID NO: 26. This invention designs the target sequence hybridization probe so that one part hybridizes with the target gene and the other part hybridizes with the fluorescent reporter probe. The fluorescence value of the fluorescent reporter probe can identify or differentiate target cells. Using this kit, neutrophils can be identified or classified into neutrophil subsets that are positive for CXCL8, LYZ, IL1R2, S100A12, and IFI16 genes. These gene-positive neutrophil subsets can be used to diagnose early-stage cancer.
Owner:SUN YAT SEN UNIV

Hybrid probe mixed solution for radiation biological dose detection and preparation method and product thereof

The invention relates to a hybridization probe mixed solution for radiation biological dose detection as well as a preparation method and a product thereof, and belongs to the field of molecular cell genetics. The technical problem to be solved is to provide a hybridization probe mixed solution with significantly improved chromosome distortion recognition accuracy and sensitivity, higher detection efficiency and better repeatability. According to the key point of the technical scheme, the hybridization probe mixed solution is composed of a probe and a hybridization buffer solution, the volume ratio of the probe to the hybridization buffer solution is 1: (50-1000); the hybridization buffer solution is a 40%-70% formamide solution containing 10 to 20 mM of Tris-HCl or PBS (Phosphate Buffer Solution). When the hybridization probe mixed solution is used for radiation biological dose detection, the distortion identification accuracy and sensitivity are high, the radiation dose estimation precision is high, and the operation is convenient.
Owner:NAT INST FOR RADIOLOGICAL PROTECTION & NUCLEAR SAFETY CHINESE CENT FOR DISEASE CONTROL & PREVENTION

Systems, methods, and compositions for digital drop-off assays

PendingUS20260110017A1Microbiological testing/measurementHybridization probeAssay
The present disclosure provides methods, systems, and compositions for the multiplexed detection and quantification of multiple analytes from a sample. Analytes may be nucleic acid analytes. Detection of analytes may comprise contacting one or more samples with primers and / or hybridization probes to generate cumulative signal measurements. The methods may comprise digital PCR or may comprise partitioning a sample into multiple partitions.
Owner:CHROMACODE INC

Methods, systems and compositions for detection of multiple analytes

PendingUS20250263781A1Microbiological testing/measurementHybridization probeAnalyte
The present disclosure provides methods, systems, and compositions for the multiplexed detection and quantification of multiple analytes from a sample. Analytes may be nucleic acid analytes. Detection of analytes may comprise contacting one or more samples with primers and / or hybridization probes to generate cumulative signal measurements. The methods may comprise digital PCR or may comprise partitioning a sample into multiple partitions.
Owner:CHROMACODE INC

Preparation method of fluorescence in situ hybridization kit based on hybridization chain reaction (HCR)

The invention belongs to the technical field of molecular biology, and discloses a preparation method of a fluorescence in situ hybridization kit based on a hybridization chain reaction (HCR), the core components of the kit comprise a hybridization probe, an amplification probe, a washing liquid, a confining liquid, protease K, HRP-mouse anti-digoxin, and a TSA developing liquid 520 nm. According to the FISH detection system combined with the HCR signal amplification technology, when a hybridization probe and an amplification probe are simultaneously combined to a position adjacent to a target sequence, a small section of sequence at the top end can trigger a branched HCR reaction to form a macromolecular nucleic acid aggregate. Signal amplification of HCR is achieved through cascade hybridization reaction, detection sensitivity and specificity can be remarkably improved, and meanwhile the problem of background noise caused by a traditional enzymatic method is avoided. The kit disclosed by the invention is wide in sample application range, and can be used for positioning analysis of target RNA of samples such as paraformaldehyde or formalin-fixed animal and plant tissues, paraffin or frozen sections, cells and the like, and high-sensitivity detection of the single cell level of non-coding RNA.
Owner:HANGZHOU BORRICK BIOTECHNOLOGY CO LTD

Composition and methods for hybridization

ActiveUS12662698B2Microbiological testing/measurementHybridization probeCarboxylic acid
The present invention relates to a composition for use in hybridization, the composition comprising: (a) at least one hybridization probe (“component (a)”); (b) at least one polar protic or polar aprotic solvent (“component (b)”) having a cyclic molecule structure; and (c) at least one carboxylic acid amide and / or salts thereof (“component (c)”), in an amount of more than 10 vol %, based on the composition. The invention furthermore relates to a use of this composition, and to methods for detecting nucleic acids and / or chromosomal aberrations in a biological sample by way of hybridization, using the composition.
Owner:42 LIFE SCI GMBH & CO KG

Nucleic acid assays using click chemistry bioconjugation

PendingUS20250270622A1Microbiological testing/measurementHybridization probeNucleic acid detection
Provided herein are methods of sequencing comprising click chemistry bioconjugation. In some embodiments, target polynucleotide sequences on the same or different molecules are contacted with and hybridize to probes comprising click functional groups. Probes (e.g., reading probes) hybridizing to adaptor sequences adjacent to different sequences of interest (e.g., barcodes to be sequenced) can be hybridized simultaneously in large pools. In some embodiments, the provided methods achieve multiplexing without requiring separate hybridization of probes (e.g., reading probes) for each sequencing-by-ligation cycle, thereby reducing total hybridization time which is typically a most time-consuming step in in situ technologies. In some aspects, the hybridized probes (e.g., reading probes) are clicked onto detectable probes to analyze a sequence of a target polynucleotide in a sequencing-by-ligation fashion.
Owner:10X GENOMICS INC

Methods and compositions for genomic target enrichment and selective DNA sequencing

It has been established that one or more large double stranded DNA fragments (each 2,000 to 40,000 base pairs in size) can be captured and isolated from genomic DNA fragments using sequence specific PNA hybridization probes. Compositions and methods for enrichment of a multiplicity of long DNA sequences selected from the genome of any eukaryote are provided. Capture is performed using multiple PNA molecules with gamma-modified chiral backbones, comprising a mixture of neutral and positive chemical groups. Two or more PNA probes with covalently bound haptens, preferably biotin, target each DNA domain of interest for capture, isolation, and subsequent sequencing analysis of the multiplicity of enriched targets, including DNA methylation sequencing. The methods include enhancement of probe-DNA binding specificity through single strand binding proteins (SSB).
Owner:PETAOMICS INC

Method for rapidly identifying chromosome ploidy of cucumber horticultural variety

The invention discloses a method for rapidly identifying chromosome ploidy of a cucumber horticultural variety. The method mainly comprises the following steps: preparing cucumber somatic cell interphase nuclear flakes; preparing a 5S rDNA (ribosomal deoxyribonucleic acid) probe / centromere sequence (Type-III) probe; and carrying out FISH hybridization. FISH hybridization signals of the 5S rDNA probe / centromere sequence (Type-III) probe are very stable in the whole cell cycle of the cucumber and are convenient to count, so that the chromosome ploidy of the cucumber variety can be accurately identified no matter whether the cell is in an interphase or a division phase. The invention provides a rapid and accurate identification method for chromosome ploidy identification of cucumber haploids or some growing point materials difficult to obtain root tips and the like.
Owner:NANJING AGRICULTURAL UNIVERSITY

Albumin mRNA detection kit for auxiliary diagnosis of liver cancer

The invention discloses an albumin mRNA (messenger Ribonucleic Acid) detection kit for auxiliary diagnosis of liver cancer, which comprises nucleic acid probes with sequences as shown in SEQ ID NO: 1-20 and can be combined with albumin mRNA. The 5'or 3 'tail end of the nucleic acid probe comprises a linker 1 combination region base sequence, the linker 1 combination region base sequences of two adjacent nucleic acid probes are combined to form a linker 1, the linker 1 does not participate in complementary pairing with albumin mRNA, and the nucleic acid probe group is obtained through a cascade amplification process. The albumin mRNA detection kit provides 10 groups of in-situ hybridization probes targeting different areas of albumin mRNA, false negative results caused by RNA degradation can be avoided, mRNA signals can be amplified by hundreds of times through a cascade amplification process, and the sensitivity of an in-situ hybridization detection technology is greatly improved.
Owner:SHANDONG RES INST OF TUMOUR PREVENTION TREATMENT

Marker composition for detecting or diagnosing lung cancer, product and application of marker composition

The invention discloses a marker composition for lung cancer detection or diagnosis, a product and application thereof, and relates to the technical field of lung cancer diagnosis. The marker composition provided by the invention has the advantages of high specificity and high sensitivity, the false positive rate of the marker composition provided by the invention is zero due to 100% specificity, and unnecessary anxiety, unnecessary radiation exposure and further invasive examination can be avoided. Based on the marker composition for lung cancer detection or diagnosis provided by the invention, lung cancer diagnosis products, such as reagents, kits, chips, hybridization probes or sequencing libraries, can be further developed. And rapid, high-sensitivity and high-specificity detection or diagnosis of the lung cancer can be realized.
Owner:JIAXING YUNYING MEDICAL INSPECTION CO LTD

Liquid hybridization probe pool, kit, and combined detection method for multiple pathogens and drug resistance genes

This invention discloses a liquid-phase hybridization probe pool for the joint detection of multiple pathogens and drug resistance genes, designed according to the target regions of the target pathogens and drug resistance genes. The probes are of varying lengths from 30 to 100 nt, including target-specific sequences complementary to the target region and conjugate sequences complementary to adjacent probes. The 5' and 3' ends of the probes are modified with conjugate sequences A and B, respectively, enabling specific binding between adjacent probes through end-pairing. Conjugate sequence A is shown in SEQ ID No. 601, and conjugate sequence B is shown in SEQ ID No. 602. This invention utilizes library construction and specific probe pool hybridization to shorten the capture time to 30 min, significantly outperforming traditional methods. This optimization not only reduces operation time and complexity and minimizes human error but also maintains high sensitivity and specificity, enabling efficient capture of target nucleic acids in complex samples, providing high-quality templates for subsequent sequencing, and supporting the joint detection of multiple respiratory pathogens and drug resistance genes.
Owner:BEIJING YOUAN HOSPITAL CAPITAL MEDICAL UNIV

Method for capturing in-situ interaction protein of ready-to-use RNA (Ribonucleic Acid)

The invention belongs to the technical field of biology, and discloses a capturing method of ready-to-use RNA (Ribonucleic Acid) in-situ interaction protein. The method comprises the following steps: S1, adding a biotin-labeled FISH probe into a cell suspension; s2, then adding streptavidin to be labeled with horse radish peroxidase (Streptavidin-HRP), and carrying out enzyme deactivation on the horse radish peroxidase; s3, washing off non-specific binding; and S4, adding biotin phenol and a hydrogen peroxide substrate to trigger a biotinylation labeling reaction. According to the method, a ready-to-use RNA in-situ proximity biotinylation labeling technology without genetic manipulation is established through fusion RNA-FISH in-situ hybridization and proximity labeling technologies, proximity labeling enzyme can be directly guided to interested RNA through an RNA hybridization probe in a fixed cell through the technology, then a proximity biotinylation labeling reaction is carried out, and the RNA in-situ proximity biotinylation labeling technology is established. The method comprises the following steps of: adding a biotin label to interacting protein adjacent to RNA (Ribonucleic Acid), so that the protein can be enriched by streptavidin-beads for mass spectrum identification.
Owner:FUDAN UNIV SHANGHAI CANCER CENT

Method for measuring positive rate of cells for expressing exogenous therapeutic genes by RNA (Ribonucleic Acid) hybridization and flow cytometry

The invention provides a method for measuring the positive rate of cells expressing exogenous therapeutic genes by combining RNA (Ribonucleic Acid) hybridization and flow cytometry. The detection method comprises the following steps: designing a specific in-situ hybridization probe aiming at mRNA (Messenger Ribonucleic Acid) expressed by a target gene, carrying out RNA probe in-situ hybridization staining in the cells, and distinguishing specific cell subgroups by combining the single cell resolution of flow cytometry. A feasible detection method is provided for highly personalized and multivalent TCR and other cell treatment samples which do not have specific antibodies or cannot detect the positive rate by using a unique antibody, and the design space for designing the specific target RNA probe is larger and the difficulty is lower than that for designing the specific antibody. Comprising the following steps: fixing cell morphology and RNA, permeabilizing / breaking a cell membrane, fixing / perforating a cell nucleus, digesting intracellular and intracellular free single-stranded DNA, carrying out RNA probe hybridization and signal amplification, and carrying out flow detection.
Owner:HANGZHOU CHENGYUAN BIOTECHNOLOGY CO LTD

A method for constructing sequencing library for removing human-derived nucleic acid and application thereof

The application discloses a sequencing library for removing human-derived nucleic acid and a construction method and application thereof, and the construction method comprises the following steps: fragmentizing nucleic acid and adding sequencing adapters, constructing a DNA or RNA library, or constructing a RNA and DNA co-library, then taking the library with the added sequencing adapters as a template, performing denaturation annealing on the library and specific human-derived hybridization probes, and performing digestion on the library by using DSN enzyme, and in the renaturation process, human-derived nucleic acid with a higher content is preferentially annealed with the human-derived hybridization probes to form double strands, which are degraded by the DSN enzyme, pathogenic microorganism with a low content is slowly renatured and remains in a single-stranded state, and cannot be digested by the DSN enzyme, and the human-derived nucleic acid is effectively removed, and the nucleic acid of the pathogenic microorganism is further enriched through subsequent PCR. The method can effectively reduce the proportion of human-derived nucleic acid in the library, and maximize the retention of nucleic acid information of the pathogenic microorganism.
Owner:JIANGSU BIOPERFECTUS TECH CO LTD

Application of hybridization probe to target binding in sample containing single-stranded DNA binding protein

The invention discloses an application of a hybridization probe in binding with a target in a sample containing a single-stranded DNA binding protein, the hybridization probe at least comprises a segment of nucleic acid sequence, and the nucleic acid sequence comprises at least one of the following items: modification of a basic group, modification of ribose and modification of phosphate. In the application of the invention, the hybridization probe can efficiently hybridize with the target in the presence of the single-stranded DNA binding protein.
Owner:CHANGZHOU FLUOSCIENCE MEDICAL TECHNOLOGY CO LTD

SV molecular marker for specific series insertion of papaya Y linkage region and application of SV molecular marker

The invention provides a papaya Y linkage region specific serial insertion SV molecular marker and application thereof, and belongs to the technical field of molecular biology, the SV molecular marker is HSY3-TR-13bp, and is used for identifying the gender of papaya; the primer pair is used for detecting the SV molecular marker; the hybridization probe is used for detecting the SV molecular marker; preparing a kit and a hybridization chip by using the primer pair or the hybridization probe; the primer pair, the hybridization probe, the kit or the hybridization chip are used for identifying the gender of the papaya. According to the specific haplotype SV marker, rapid sex identification of the amphoteric plants in the seedling stage can be achieved, the identification accuracy of the HSY3 type (belonging to dominant haplotype in market cultivated species) amphoteric plants is 100%, the screening efficiency of the seedlings of the amphoteric plants in the papaya seedling breeding process is improved, the orchard planting density is increased, and the labor management cost, the fertilizer cost and the like are reduced.
Owner:SANYA RES INST OF CHINESE ACAD OF TROPICAL AGRI +1