Methods and kits for the detection of toxic cyanobacteria in a sample by analyzing the sample for the presence antibodies raised in a host, where the presence of antibodies is indicative of toxic cyanobacteria, are described.

Methods for detecting and quantifying one or more microcystin compounds in a sample are described. The methods may include a preconcentration step, and generally utilize an LC-MS or LC-MS/MS analysis with an Orbitrap Fusion mass spectrometer. The methods provide excellent recoveries and limits of quantification of microcystins.

A method for extracting an analyte in a sample is described. A sample and a solution in a microwave-extraction vial are microwave-heated and agitated. A vapor produced in the vial can be extracted into a liquid-phase medium contained in a porous membrane bag situated in the vial. The liquid-phase medium containing the vapor extract may then be analyzed for an analyte with gas chromatography-mass spectrometry.

A method for extracting an analyte in a sample is described. A sample and a solution in a microwave-extraction vial are microwave-heated and agitated. A vapor produced in the vial can be extracted into a liquid-phase medium contained in a porous membrane bag situated in the vial. The liquid-phase medium containing the vapor extract may then be analyzed for an analyte with gas chromatography-mass spectrometry.

An excellent photosensitivity is exhibited by a protein including, at a position or positions corresponding to one or two or more positions selected from the group made of the following (1) to (3) in a first amino acid sequence represented by SEQ ID NO: 1: (1) positions 39, 94, 98, 102, 110, 113, 114, 162, 224, 225, 230, 231, and 235, (2) positions 53, 61, 68, 74, 76, 80, 130, 137, 194, 195, 198, 200, 204, 205, 209, 210, 253, and 254, and (3) positions 46, 83, 84, 87, 90, 91, 116, 117, 120, 124, 139, 142, 143, 146, 173, 214, 216, 217, 238, 242, and 245, an amino acid residue different from that in the first amino acid sequence, and that has channel activity.

A method for extracting an analyte in a sample is described. A sample and a solution in a microwave-extraction vial are microwave-heated and agitated. A vapor produced in the vial can be extracted into a liquid-phase medium contained in a porous membrane bag situated in the vial. The liquid-phase medium containing the vapor extract may then be analyzed for an analyte with gas chromatography-mass spectrometry.

The present invention relates to a method for rapid detection of toxicity comprising preparing a plant gel agar and a sample; mixing the agar gel with the sample to form a mixture; and measuring a coagulation time of the mixture to determine the cytotoxicity of the sample.

An excellent photosensitivity is exhibited by a protein including, at a position or positions corresponding to one or two or more positions selected from the group made of the following (1) to (3) in a first amino acid sequence represented by SEQ ID NO: 1: (1) positions 39, 94, 98, 102, 110, 113, 114, 162, 224, 225, 230, 231, and 235, (2) positions 53, 61, 68, 74, 76, 80, 130, 137, 194, 195, 198, 200, 204, 205, 209, 210, 253, and 254, and (3) positions 46, 83, 84, 87, 90, 91, 116, 117, 120, 124, 139, 142, 143, 146, 173, 214, 216, 217, 238, 242, and 245, an amino acid residue different from that in the first amino acid sequence, and that has channel activity.

A method of sorting cells on a FACS includes providing a culture of cells stained with a dye. The dye is excited using photons at a first wavelength. A fluorescence and emission of the dye is collected at a second wavelength. Droplets of the cells are produced by pumping the cell culture at a first pressure through a nozzle having a nozzle diameter. The droplets are produced at a first frequency. The cells are sorted by a desired property. The desired property can include sorting the cells by size using at least one of a forward scatter area (FSC-A), a forward scatter height (FSC-H), a forwards scatter width (FSC-W), side scatter area (SSC-A), a side scatter height (SSC-H) and a side scatter width (SSC-W) of the fluorescence of the dye to determine a size of the cells.

A method and system for direct quantification of the concentration of biomolecules in algal biomass. The biomolecules include lipids, proteins, and carbohydrates. An algae slurry is cultivated within a cultivation vessel, and algal biomass is harvested therefrom. A portion of biomass is analyzed using solvent-lipid analysis to extract lipids and nuclear magnetic resonance spectroscopy is used to quantify the biomolecular concentration of the biomass.