Abstract: An instrument and a method for conveniently collecting nucleic acids from a biological nucleic acid-containing sample are provided. A nucleic acid-capturing tip having silica-containing solid phases enclosed therein in such a state as being capable of coming into contact with a liquid, wherein the solid phases have a water-flowing regions and the average interval among solid phases in the water-flowing regions is regulated to 25 ?m or less.

Abstract: An instrument and a method for conveniently collecting nucleic acids from a biological nucleic acid-containing sample are provided. A nucleic acid-capturing tip having silica-containing solid phases enclosed therein in such a state as being capable of coming into contact with a liquid, wherein the solid phases have a water-flowing regions and the average interval among solid phases in the water-flowing regions is regulated to 25 ?m or less.

Abstract: A method to extract RNA with high purity from biological materials containing RNA in a safe, rapid, and simple procedure and a method to analyze it are provided. The procedure includes the steps of mixing a biological material containing RNA with a predetermined concentration of a chaotropic agent and a predetermined concentration of an organic solvent, allowing the mixed solution to contact a nucleic acid-binding solid phase, washing the nucleic-acid binding solid-phase to which RNA is bound, and eluting RNA from the nucleic-acid binding solid-phase having the bound RNA. Furthermore, the obtained RNA is analyzed by reverse transcriptase-polymerase chain reaction (RT-PCR) or the like.

Abstract: The object of the present invention is to provide a nucleic acid purification method and purification apparatus characterized by high washing efficiency where contamination does not occur and liquid does not remain in the nozzle tip. The present invention provides a tip containing the solid phase capturing a nucleic acid characterized in that washing solution is fed into said tip unidirectionally from head to end.

Abstract: The object of the present invention is to provide a nucleic acid purification method and purification apparatus characterized by high washing efficiency where contamination does not occur and liquid does not remain in the nozzle tip. The present invention provides a tip containing the solid phase capturing a nucleic acid characterized in that washing solution is fed into said tip unidirectionally from head to end.

Abstract: The object of the present invention is to provide a nucleic acid purification method and purification apparatus characterized by high washing efficiency where contamination does not occur and liquid does not remain in the nozzle tip. The present invention provides a tip containing the solid phase capturing a nucleic acid characterized in that washing solution is fed into said tip unidirectionally from head to end.

Abstract: A chemical analysis device has a motor, a holder disk to be rotated by the motor, a plurality of inspection cartridges, a penetrator for penetrating the inspection cartridges, a heater and a detector. The inspection cartridge has a substrate including containers formed as recesses and a flow path, and a cover is mounted on the substrate to cover the containers and flow path. By a centrifugal force generated by a rotation of the holder disk, a liquid is moved through the flow path from the container at a radially inner side with respect to a rotational axis to the container at a radially outer side with respect to the rotational axis.

Abstract: When a plurality of liquids are simultaneously sucked using a plurality of suction paths connected to a single pump, one suction end may hinder other acts of suction. A multiple valve for connecting each suction path and the pump in a one-by-one manner is disposed between the plurality of suction paths and the pump. Suction is conducted while the communication between the suction paths and the pump is successively switched in a time-sharing manner. At a certain period of time, the pump and a given path is independent of other suction paths. Whereby, suction can be conducted without being influenced by suction ends of other suction paths.

Abstract: A solution such as a washing liquid can be passed through a separation column such as a nozzle tip having a solid phase quickly and reliably, thereby achieving improvements in throughput. A sample processing device comprises a separation column having a carrier capable of capturing a target substance, a liquid supply passage capable of supplying a liquid from one end portion of the separation column to the other end portion thereof, and a communication passage disposed independently of the liquid supply passage and capable of providing communication between the inside of the separation column and the outside. The communication between the inside of the separation column and the outside by the communication passage is controlled.

Abstract: In a chemical analyzer, an accommodation part accommodates a structure that stores a reagent being caused to react with a sample and has a reaction region, in which the sample and the reagent react with each other. Further, a detection mechanism detects the sample after reaction. The structure is formed with a reagent cartridge that stores a reagent, and an analysis cartridge comprising a connection part, to which the reagent cartridge is connected, a reagent flow path, through which the reagent flows, a sample flow path, through which the sample flows, and a reaction region communicated to the reagent flow path and the sample flow path. A side surface of the reagent cartridge and a side surface of the analysis cartridge are arranged in opposite to each other and connected to each other through the connection part.

Abstract: A chemical analyzing apparatus accommodates therein a structure for retaining a sample and reagents. A detecting mechanism detects the sample after reaction with a reagent. After or during extraction of a biological substance from the sample in the structure, a temperature of a fluid in a space around the structure is controlled to a value which is suitable for enzyme.

Abstract: A method to extract RNA with high purity from biological materials containing RNA in a safe, rapid, and simple procedure and a method to analyze it are provided. The procedure includes the steps of mixing a biological material containing RNA with a predetermined concentration of a chaotropic agent and a predetermined concentration of an organic solvent, allowing the mixed solution to contact a nucleic acid-binding solid phase, washing the nucleic-acid binding solid-phase to which RNA is bound, and eluting RNA from the nucleic-acid binding solid-phase having the bound RNA. Furthermore, the obtained RNA is analyzed by reverse transcriptase-polymerase chain reaction (RT-PCR) or the like.

Abstract: The present invention absorbs and captures nucleic components from various specimens by a single stationary phase and finally recovers the nucleic components by eluting the captured nucleic components from the stationary phase. This invention enables recovery of nucleic components without reducing the concentrations of nucleic acids and detection of specific nucleic components such as specific viruses.

Abstract: The object of the present invention is to provide a nucleic acid purification method and purification apparatus characterized by high washing efficiency where contamination does not occur and liquid does not remain in the nozzle tip. The present invention provides a tip containing the solid phase capturing a nucleic acid characterized in that washing solution is fed into said tip unidirectionally from head to end.

Abstract: Provided herein are an apparatus and a method for efficiently recovering nucleic acids from a nucleic acid-containing solution by causing the nucleic acid-containing solution to come into stable contact with a solid phase in a nucleic acid-capturing tip.

Abstract: The present invention absorbs and captures nucleic components from various specimens by a single stationary phase and finally recovers the nucleic components by eluting the captured nucleic components from the stationary phase. This invention enables recovery of nucleic components without reducing the concentrations of nucleic acids and detection of specific nucleic components such as specific viruses.

Abstract: A nucleic-acid amplifying apparatus comprising: a flow passage, through which a reaction fluid containing a sample containing a nucleic acid and a reagent flows, said flow passage including, a flow passage branch portion, at which the flow passage branches into a plurality of branch flow passages, a junction portion, at which the plurality of branch flow passages join, and a joined flow passage, through which the reaction fluid as joined is conducted; and a heating mechanism having a plurality of set temperature zones provided on the branch flow passages.

Abstract: An analyzer and a structure for analysis with high performance are provided which can reduce contamination between the reagents when the valve components or a plurality of reagents are included.

Abstract: A solution such as a washing liquid can be passed through a separation column such as a nozzle tip having a solid phase quickly and reliably, thereby achieving improvements in throughput. A sample processing device comprises a separation column having a carrier capable of capturing a target substance, a liquid supply passage capable of supplying a liquid from one end portion of the separation column to the other end portion thereof, and a communication passage disposed independently of the liquid supply passage and capable of providing communication between the inside of the separation column and the outside. The communication between the inside of the separation column and the outside by the communication passage is controlled.

Abstract: A process for recovery of nucleic acids comprises a first step of bringing a sample containing ribonucleic acid and deoxyribonucleic acid into contact with a nucleic acid-binding solid phase; and a second step of bringing a first eluate at not lower than 4° C. and not higher than 20° C. into contact with said nucleic acid-binding solid phase, which has captured ribonucleic acid and deoxyribonucleic acid contained in said sample, thereby causing at least deoxyribonucleic acid to be eluted into the first eluate.