A system separates and in-situ analyzes a discrete sample of multiphase fluid. The system includes a separation vessel having a first inner chamber for separating a discrete sample of multiphase fluid into liquid phases including an aqueous liquid phase and a nonporous liquid phase, and a built-in water analysis unit. The built-in water analysis unit includes an analytical cell disposed inside the first inner chamber of the separation vessel, the analytical cell having a second inner chamber, and at least one probe having a sensing area disposed in the second inner chamber for in-situ analysis of a sample of the aqueous liquid phase that is separated from the discrete sample of multiphase fluid in the first inner chamber and that is channeled to the second inner chamber from the first inner chamber for the in-situ analysis. The second inner chamber is defined inside the first inner chamber.

There is provided a piston of a cartridge for extracting nucleic acids comprising: a cylindrical upper body having a hollow; a lower body having two ports; a control rod module combined to the other end of the upper body to seal the other end and move up and down along the hollow; and a rotation control module that is combined to the shaft of the lower body to transmit a driving force to the lower body.

The present disclosure discloses a method for evaluating the nutritional status in plants, using visible-to-shortwave (VIS-SWIR) infrared reflectance spectroscopy of carbohydrates, particularly in almond trees. The method comprises obtaining a dry plant sample (i.e. leaves, branches and roots), digesting and grinding it to a powder, capturing predetermined spectral data of the ground plant sample, correlating said spectral data to predetermined materials and evaluating said nitrogen status of said plants according to predetermined multivariate statistical models. The data obtained from this method facilitates crop management and fertilization by providing the nitrogen status of the plants based on non-structural carbohydrates.

The present disclosure relates to a method/system for preparing encapsulated exosomes from a biological sample containing exosomes, said method comprising: a) dispersing inorganic oxide particles into a buffer solution comprising a polymer and a biological sample comprising exosomes, b) allowing the polymer to react with the inorganic oxide particles to form capsules, wherein the exosomes are inside the capsules. The present disclosure also relates to a method/system for isolating and purifying encapsulated exosomes, said method comprising: a) preparing an aqueous micellar system comprising at least one surfactant, and at least one salt; b) mixing a biological sample containing encapsulated exosomes with the aqueous micellar system from step a); c) allowing the aqueous micellar system to phase separate, wherein the surfactant partitions substantially into one phase, and the other phase has a lower concentration of surfactant; and d) obtaining the encapsulated exosomes from the capsule-rich phase.

An analytical pretreatment method of microplastics includes: placing the microplastics separated by a gravity separation treatment in a sieve; immersing the sieve containing the microplastics in pure water having a depth smaller than a height of the sieve; and lifting the sieve up from the pure water and drying the microplastics contained in the sieve with a constant temperature dryer. Thus, the analytical pretreatment method of microplastics is capable of reducing the influence of a gravity separation solution on the analysis result of the microplastics.

The present disclosure relates to the development of novel immunoassays for the detection of SARS-CoV-2 or secreted spike protein (or fragments thereof) in saliva, nasal mucosal sample, throat samples, or nasopharyngeal samples.

Disclosed is a leaching solution composition for extracting available phosphate in soil, the composition including 100 parts by weight of a leaching solution containing acetic acid, lactic acid, ammonium fluoride, ammonium sulfate, and sodium hydroxide, of which the weights are 110% of the weights of constituent ingredients of a leaching solution for extracting available phosphate in soil, used in the Lancaster method and 0.001 parts by weight of a bromocresol green indicator.

A process for rendering excavation material inert for the purpose of their analysis, of their storage and/or of their valorisation. The process for inerting the excavation material includes adding an organic acid, of a complexing agent or of a diaminotetracarboxylic acid to the excavation material, the complexing agent being chosen from a sugar alcohol, a cationic surface-active agent and their mixtures. Also, a method of determining the concentration by weight of a polluting inorganic element included in an excavated material, a method of storage of the inert excavation material, and a method of valorising the inerted material.

A method for differentially lysing a liquid sample or target material using an augmented oxidizing agent (AOA), which includes a quantity of electronically modified oxygen derivatives (EMODs). The method reduces or eliminates total dissolved solids (TDS), total suspended solids (TSS), Biologic Oxygen Demand (BOD), microbial concentration, biofilms and other content in the liquid target material known or suspected to contain animal fluids, blood and blood cells and suspected or known to contain eukaryotic cells, microbial cells, bacteria, viruses, spores, fungi, prions, organic matter, minerals, proteins or associated structures. The BOD, TDS and TSS can be lowered or eliminated as desired. This action is directly proportional to the quantity of EMODs in the AOS applied to the liquid target material.

The present disclosure relates to a dissociation reagent for tumor tissues. The dissociation reagent does not contain collagenase or trypsin but further contains hyaluronidase or a mixture of hyaluronidase and DNase I. The present disclosure also relates to use of the dissociation reagent in dispersing tumor tissues and detecting expression level of molecular markers on cell surface by flow cytometry. The dissociation reagent of the present disclosure does not cause degradation of molecular markers on cell surface such as CD8, PD-1, Tim-3, Lag-3 and the like, thus does not affect downstream assays.