Disclosed are a composition and system for separating and detecting an alpha-fetoprotein variant, comprising a separation reagent and a detection reagent; a system for separating and detecting an alpha-fetoprotein variant and a use thereof; and a kit for separating and detecting the alpha-fetoprotein variant. By means of the composition and system for separating and detecting the alpha-fetoprotein variant, and the use thereof, primary liver cancer can be indicated early on, the sensitivity is high, and the method is rapid, simple and automated.

The present invention relates to a gas-liquid separator for a chromatography system, comprising: a) a separating region having an inlet nozzle, a baffle unit and a gas distribution unit; (b) a dividing region having a liquid outlet; and (c) a gas discharge region having a gas outlet; wherein the separating region is connected to the dividing region by a separating opening and the distance of the inlet nozzle from the baffle unit is greater than the smallest longitudinal extension of the separating opening and the inlet nozzle is configured such that a gas-liquid stream directed through the inlet nozzle can act on the baffle unit. The present invention further relates to a chromatography system comprising a separator according to the invention and to a chromatography method wherein the separator is used.

An ion chromatography system includes a separation column configured to separate components of a solution; a non-destructive detector; and a concentrator configured to capture components of a check standard after they leave the conductivity non-destructive detector; and release the components of the check standard to the separation column.

The present invention relates to a gas-liquid separator for a chromatography system, comprising: (a) a separating region having an inlet nozzle, a baffle unit and a gas distribution unit; (b) a dividing region having a liquid outlet; and (c) a gas discharge region having a gas outlet; wherein the separating region is connected to the dividing region by a separating opening and the distance of the inlet nozzle from the baffle unit is greater than the smallest longitudinal extension of the separating opening and the inlet nozzle is configured such that a gas-liquid stream directed through the inlet nozzle can act on the baffle unit.

The present invention further relates to a chromatography system comprising a separator according to the invention and to a chromatography method wherein the separator is used.

A system and method for determining an efficiency of gas extraction. A chamber allows inflow and outflow of the drilling fluid. An amount of gas extracted from a drilling fluid flowing through the chamber at a constant rate during a dynamic process is measured. A dissolution curve is obtained indicative of a gas remaining in the chamber after the dynamic process. An amount drawn from the chamber during a static process subsequent to the dynamic process is measured. An amount of gas from the drilling fluid during the static process is determined from a difference between the amount of gas drawn from the chamber during the static process and an amount of gas indicated by the dissolution curve. The gas extraction efficiency is determined from a ratio of the amount of gas extracted during the static process and the amount of gas extracted during the dynamic process.

A method of sampling ingredients of an oil-bearing inclusion includes a) providing a first container and a second container, an external diameter of the first container being smaller than an internal diameter of the second container, and the first and second containers both being transparent; b) adding a solvent into the first container and sealing said first container; c) adding an oil-bearing inclusion sample into the second container, and putting the first container that contains the solvent and is sealed in step b) into the second container; and d) using a laser to ablate the oil-bearing inclusion sample contained in the second container that is sealed in step c), and using the laser to break an end portion of the first container close to the sample on condition that the second container is maintained complete, so as to allow the solvent in the first container to enter the second container.

Systems and methods are provided for determining a content of a hydrocarbon or other compound, such as a C.sub.3 to C.sub.7 hydrocarbon, in a condensed steam sample. Cooled steam condensate can be flowed through a sample chamber including an inner overflow tube. When the flow stops, water can be drained from the sample chamber, and then the sample chamber can be opened to allow fluid communication with a vapor chamber above the sample chamber. This can allow hydrocarbons in the condensed steam (and/or other gas) to be transferred from the sample chamber into the vapor chamber. The vapor chamber can then be isolated from the sample chamber. At least a portion of the content of the vapor chamber can then be passed to a detection volume, such as the characterization cell for a gas chromatography system.

The disclosure discloses a method for quickly and accurately analyzing polyphenol content in rapeseed oil, and belongs to the field of analysis of natural compounds. The separation method of the disclosure uses acetonitrile-water as an extractant to extract polyphenols from the rapeseed oil, and cooperates with a C.sub.18 adsorbent for purification, and then performs separation and purification. Compared with the traditional liquid-liquid extraction and solid-phase extraction, the method has an average recovery rate of polyphenols in the rapeseed oil of 81.31% to 102.95%, and RSDs of 0.86% to 8.03%, and has higher accuracy and precision. The method of the disclosure not only uses less organic reagents and causes less environmental pollution, but also reduces matrix interference and improves purification efficiency through optimization of the adsorbent. The method of the disclosure not only is simple to operate and low in cost, but also has less matrix interference and accurate results, and is suitable for the qualitative and quantitative determination of polyphenols in the rapeseed oil.

The invention relates to a method for the chromatographic purification of at least one cannabinoid compound, wherein the method comprises a main purification stage comprising the steps of: injecting an initial mixture comprising the at least one cannabinoid compound and one or more additional compounds onto a main stationary phase comprising silica particles, the silica particles comprising amino and/or diol groups; performing an elution with an elution solution, and collecting one or more elution fractions; and optionally, washing the main stationary phase with a washing solution and collecting one or more washing fractions; at least one of the elution fractions or washing fractions containing the at least one cannabinoid compound purified from the one or more additional compounds.

A method for extracting pharmacogenetic DNA from dried blood that is retained in a solid resin collection device includes one or more of the steps of combining the dried blood and at least a portion of the solid resin collection device in a first vessel, sonicating the first vessel containing the dried blood and at least a portion of the solid resin collection device, moving at least some of the contents of the first vessel including the portion of the solid resin collection device to a solid resin spin column, adding an elution buffer to the solid resin spin column, centrifuging the solid resin spin column so that at least some of the contents of the solid resin spin column are transferred to a second vessel, and processing the contents of the second vessel by conducting one of capillary electrophoresis, Next-Generation Sequencing, DNA sequencing or genotyping, and mass spectrometry-based sequencing on the contents of the second vessel.