摘要:
A chemical reaction cartridge enabling chemical reaction to be stably and safely carried out therein, and a method of using the same are provided. A chemical reaction cartridge is provided with a substrate (1), and an elastic member 2 overlaid on the substrate (1). A recess of a predetermined shape, depressed toward the top surface of the elastic member (2) is formed in the back surface of the elastic member (2). The recess creates space between the substrate (1), and the elastic member (2), thereby making up a well (21), for holding the main ingredient of the epoxy adhesive, a flow path (22) communicating with the well (21), a well (23) for holding a curing agent for the epoxy adhesive, a flow path (24) communicating with the well (23), a mixing part (25) for mixing the main ingredient with the curing agent, and a discharge path (26) for discharging a mixture. While the chemical reaction cartridge is not in use as yet, the flow paths (22, 24), and the discharge path (26) are closed, so that the wells (21, 23) are, in effect, in a hermetically sealed condition. The mixing part (25) is made up of a plurality of flow paths (25a) intersecting each other. The respective starting ends of the flow paths (25a) are each linked with the flow path (22), or the flow path (24), and the respective terminals of the flow paths (25a) are linked with the discharge path (26). The terminal of the discharge path (26) communicates with the outside via an end face of the cartridge.
摘要:
An amount of fluorescent light (5) generated from the specimen (4) is quantitatively measured as "a light-amount value per unit area traceable to the national standard" instead of in terms of a ratio (a ratio value) as in the past. A method for measuring a fluorescent light amount, whereby a specimen (4) is irradiated with excitation light (2), and fluorescent light (5) generated from the specimen (4) is measured by a light-receiving element via a receiving optical system (6), said method comprising the steps of irradiating the specimen (4) with excitation light (2) having a light-amount value per specified unit area traceable to the national standard, and designated on the surface of the specimen (4) beforehand, causing the light-receiving element to measure the fluorescent light (5) generated from the specimen (4) via the receiving optical system (6), and computing a fluorescent light-amount as measured by the light-receiving element via the receiving optical system (6) on the basis of an excitation light-amount per the specified unit area, optical coefficients of the receiving optical system (6), and the acceptance coefficient of the light-receiving element, thereby working out a light amount value per the unit area traceable to the national standard.
摘要:
A cartridge capable of making effective use of a sample is provided. A blood sample is injected into a well (21) via an injection path (41) by use of a syringe, and so forth. A roller (6), in a state as kept pressed into contact with the cartridge, is rotated rightward, whereupon an elastic member (2) undergoes elastic deformation to cause the blood sample held in the well (21), and a liquid solvent held in a well (22) to reach a well (23), and the blood sample is thereby mixed with the liquid solvent. Since the liquid solvent contains surfactant, blood cells are destroyed in the well (23). The liquid solvent reaches a well (26) via a flow path (45). At this point in time, magnetic particles held in the well (25), and a cleaning liquid held in the well (24) are merged with the mixed liquid in the well (26). A magnet (7) is shifted from a position corresponding to the well (26) to a position corresponding to the well (31) along the flow path (46), thereby separating and transferring DNA caught by the magnetic particles to the well (31). Residue inside the well (26) after removal of DNA is transferred to a well (54) by the roller. The separated biopolymers are analyzed in the cartridge.
摘要:
An amount of fluorescent light (5) generated from the specimen (4) is quantitatively measured as "a light-amount value per unit area traceable to the national standard" instead of in terms of a ratio (a ratio value) as in the past. A method for measuring a fluorescent light amount, whereby a specimen (4) is irradiated with excitation light (2), and fluorescent light (5) generated from the specimen (4) is measured by a light-receiving element via a receiving optical system (6), said method comprising the steps of irradiating the specimen (4) with excitation light (2) having a light-amount value per specified unit area traceable to the national standard, and designated on the surface of the specimen (4) beforehand, causing the light-receiving element to measure the fluorescent light (5) generated from the specimen (4) via the receiving optical system (6), and computing a fluorescent light-amount as measured by the light-receiving element via the receiving optical system (6) on the basis of an excitation light-amount per the specified unit area, optical coefficients of the receiving optical system (6), and the acceptance coefficient of the light-receiving element, thereby working out a light amount value per the unit area traceable to the national standard.
摘要翻译:(5)从所述样品(4)的定量测量为“每单位面积的光量值可溯源至国家标准”,而不是在一个比计(比例值)作为在过去产生的荧光的光量 , 一种用于测量荧光的光量,由此,试样(4)照射从试样产生的激发光(2),和荧光灯(5)方法(4)是由一个受光元件经由受光光学系统测量 (6)所述的方法包括用(2),其具有指定的每单位面积的可溯源至国家标准的光量值的激励光照射在试样(4)的步骤,和(4)预先指定的试样的表面上 ,使光接收元件来测量荧光的(5)经由所述受光光学系统(6),并计算荧光光量从样品(4)产生经由受光光学由光接收元件所测量 系统(6)每指定单位面积的激励光量的基础上,所述受光光学系统(6),以及光接收元件的受系数的光学系数,从而制定出每一个光量值 UNI T区可溯源至国家标准。
摘要:
The invention relates to a chemical reaction cartridge enabling chemical reaction to be stably and safely carried out therein upon transferring substances contained therein to thereby apply a chemical reaction, and a method of using the same. Said cartridge comprises a plurality of holding parts (60,61) for holding the substances therein, respectively, and a discharge part for discharging a mixture of the substances to the outside of the cartridge, in accordance with the deformation of the cartridge, wherein the substances each are a fluid and fine particles (62), and the mixture of the fluid and the fine particles is discharged from the discharge part.
摘要:
A cartridge capable of making effective use of a sample is provided. A blood sample is injected into a well (21) via an injection path (41) by use of a syringe, and so forth. A roller (6), in a state as kept pressed into contact with the cartridge, is rotated rightward, whereupon an elastic member (2) undergoes elastic deformation to cause the blood sample held in the well (21), and a liquid solvent held in a well (22) to reach a well (23), and the blood sample is thereby mixed with the liquid solvent. Since the liquid solvent contains surfactant, blood cells are destroyed in the well (23). The liquid solvent reaches a well (26) via a flow path (45). At this point in time, magnetic particles held in the well (25), and a cleaning liquid held in the well (24) are merged with the mixed liquid in the well (26). A magnet (7) is shifted from a position corresponding to the well (26) to a position corresponding to the well (31) along the flow path (46), thereby separating and transferring DNA caught by the magnetic particles to the well (31). Residue inside the well (26) after removal of DNA is transferred to a well (54) by the roller. The separated biopolymers are analyzed in the cartridge.