Patent classifications
C12Q2525/205
METHODS OF IDENTIFYING MULTIPLE EPITOPES IN CELLS
The invention provides methods, compositions, kits and devices for the detection of target molecules. In some embodiments, the invention allows for multiplexed target molecule detection.
DNA APTAMER-CYANINE COMPLEXES AS GENERIC COLORIMETRIC SENSORS
The subject invention provides materials and methods for single-step detection of target molecules in a sample. The methods and assays of the subject invention employ a dye-displacement strategy, in which aptamers complexed with a cyanine dye for sensitive and rapid detection of targets of interest. In the presence of a target, aptamer-target binding liberates the non-covalently bound aptamer-binding dye, resulting in optical changes that can be observed spectrophotometrically or with the naked eye. The methods and assays of the subject invention enable the colorimetric detection of targets of interest regardless of their structure, sequence, target-binding affinity, and physicochemical properties of their targets.
DNA APTAMER-CYANINE COMPLEXES AS GENERIC COLORIMETRIC SENSORS
The subject invention provides materials and methods for single-step detection of target molecules in a sample. The methods and assays of the subject invention employ a dye-displacement strategy, in which aptamers complexed with a cyanine dye for sensitive and rapid detection of targets of interest. In the presence of a target, aptamer-target binding liberates the non-covalently bound aptamer-binding dye, resulting in optical changes that can be observed spectrophotometrically or with the naked eye. The methods and assays of the subject invention enable the colorimetric detection of targets of interest regardless of their structure, sequence, target-binding affinity, and physicochemical properties of their targets.
Materials and methods for the delivery of therapeutic nucleic acids to tissues
The present disclosure provides materials and methods for the delivery of therapeutic nucleic cells (and imaging agents) to tissues.
Materials and methods for the delivery of therapeutic nucleic acids to tissues
The present disclosure provides materials and methods for the delivery of therapeutic nucleic cells (and imaging agents) to tissues.
METHODS OF IDENTIFYING MULTIPLE EPITOPES IN CELLS
The invention provides methods, compositions, kits and devices for the detection of target molecules. In some embodiments, the invention allows for multiplexed target molecule detection.
METHODS OF IDENTIFYING MULTIPLE EPITOPES IN CELLS
The invention provides methods, compositions, kits and devices for the detection of target molecules. In some embodiments, the invention allows for multiplexed target molecule detection.
SYSTEMS AND METHODS FOR DETECTING MULTIPLE ANALYTES
A method for detecting different analytes includes mixing different analytes with sensing probes, wherein at least some of the sensing probes are specific to respective ones of the analytes. The analytes respectively are captured by the sensing probes that are specific to those analytes. Fluorophores respectively are coupled to sensing probes that captured respective analytes. The sensing probes are mixed with beads, wherein the beads are specific to respective ones of the sensing probes, and wherein the beads include different codes identifying the analytes to which those sensing probes are specific. The sensing probes respectively are coupled to beads that are specific to those sensing probes. The beads are identified that are coupled to the sensing probes that captured analytes using at least fluorescence from the fluorophores coupled to those sensing probes. The analytes that are captured are identified.
SYSTEMS AND METHODS FOR DETECTING MULTIPLE ANALYTES
A method for detecting different analytes includes mixing different analytes with sensing probes, wherein at least some of the sensing probes are specific to respective ones of the analytes. The analytes respectively are captured by the sensing probes that are specific to those analytes. Fluorophores respectively are coupled to sensing probes that captured respective analytes. The sensing probes are mixed with beads, wherein the beads are specific to respective ones of the sensing probes, and wherein the beads include different codes identifying the analytes to which those sensing probes are specific. The sensing probes respectively are coupled to beads that are specific to those sensing probes. The beads are identified that are coupled to the sensing probes that captured analytes using at least fluorescence from the fluorophores coupled to those sensing probes. The analytes that are captured are identified.
FORCED INTERCALATION (FIT)-APTAMERS: PROBES BASED ON FORCED INTERCALATION
The present disclosure is directed to aptamers comprising a detectable marker situated at an internal location within the aptamer, use of the aptamers to, e.g., detect target analytes, and methods of making the aptamers. In exemplary embodiments, methods of the disclosure comprise contacting the target analyte with an aptamer comprising a detectable marker situated at an internal location within the aptamer, wherein the contacting results in binding of the target analyte to the aptamer, wherein target analyte binding to the aptamer results in restriction of internal rotation of the marker, resulting in a detectable change in the marker.