CARE-GIVING DEVICE
    3.
    发明专利

    公开(公告)号:JPH11347076A

    公开(公告)日:1999-12-21

    申请号:JP15756598

    申请日:1998-06-05

    Applicant: SHIMADZU CORP

    Abstract: PROBLEM TO BE SOLVED: To aid a care-receiver hard to stand up by him-/her-self to stand up from a laying position and make the care-receiver start to walk from a standing condition easier. SOLUTION: A support part 10 is moved by a support mechanism 1 to support the support part 10 divided corresponding to body parts and a drive mechanism 2 between a horizontal position to support a care-receiver in a laying position in the vicinity of a floor face and a standing up condition for enabling to walk and a push-out mechanism 19 is rotatably fit in a sheet part 12 constituting the support part. An operation switch 30 is turned on at the standing-up condition of the care-giving device to gradually push up the seat face to enable the care-receiver to naturally start to walk.

    CARE-GIVING DEVICE
    4.
    发明专利

    公开(公告)号:JPH11347075A

    公开(公告)日:1999-12-21

    申请号:JP15756298

    申请日:1998-06-05

    Applicant: SHIMADZU CORP

    Abstract: PROBLEM TO BE SOLVED: To aid a care-receiver hard to stand up by him-/her-self to stand up from a laying position, make the care-receiver easily ride on/down a care- giving device, and prevent the care-receiver from falling down. SOLUTION: A support mechanism 1 is moved between a horizontal position to support a care-receiver in a laying position near the floor face and a standing position to enable the care-receiver to walk and side frames 15, 16, 17 formed on both sides of a support part 10 are made horizontal when the support part 10 is near the floor face and vertical when the support part 10 elevated afar from the floor face to make the care-receiver easily ride on/down and prevented from falling down.

    NURSING DEVICE
    5.
    发明专利

    公开(公告)号:JPH11309181A

    公开(公告)日:1999-11-09

    申请号:JP12033198

    申请日:1998-04-30

    Applicant: SHIMADZU CORP

    Abstract: PROBLEM TO BE SOLVED: To remove the effect of compression or tensile force on the body of a nursed person by the movement of a support mechanism by providing a mechanism moving the support face of a support section for supporting the nursed person in the prostrated, seated and erected states. SOLUTION: Bearings 11b pivotally supporting joints, bearings 11c of a slider 22, bearings 11d of rollers 18 and an electromagnet 11e are fixed on the periphery of a support frame 11a, a moving plate 11h made of a resin and fixed with a steel plate 1g on the lower side is mounted on the support frame 11a as a back section 11 supporting the back of a nursed person, and ball bearings 11f are arranged so that the moving plate 11h can be slid against the support frame 11a. When the nursed person is moved from the prostrated state to the seated or erected state, compressive force is generated at the back of the nursed person on the back section 11 as the slider 22 of a drive device is lifted, however the moving plate 11h is slid on the support frame 11a by frictional force according to the movement of the body, and the compressive force is removed. The nursed person receives tensile force in the opposite case, however the effect on the body is likewise removed.

    INTEGRAL SPECTROSCOPE AND ON-LINE SPECTRAL MEASURING INSTRUMENT

    公开(公告)号:JPH02276927A

    公开(公告)日:1990-11-13

    申请号:JP17021789

    申请日:1989-06-30

    Applicant: SHIMADZU CORP

    Abstract: PURPOSE:To use the integral spectroscope and spectral measuring instrument even under severe environmental conditions like the actual site of a manufacture line without difficult maintenance by uniting a light guide-in part and a spectral part whose plane shape is a Rowland circle by using a material which is high in optical spatial homogeneity. CONSTITUTION:A sample of the manufacture line flows in a measurement cell 20. The luminous flux emitted by a light source lamp 18 is transmitted through a condenser lens 8 to reach a filter 14 and an entrance slit 12. Then the luminous flux which is made incident on the spectral part 6 from the slit 12 is dispersed by a concave diffraction grating 10 to form an entrance slit image at a position corresponding to an exit slit. The incidence end surface of an optical fiber 16 is arranged at the position, so monochromatic luminous flux guided by the optical fiber 16 is transmitted through the sample flowing in the measurement cell part 20, guided by an optical fiber 26 to a detector 30, and detected.

    BASE SEQUENCE DETERMINATION DEVICE

    公开(公告)号:JPS6488339A

    公开(公告)日:1989-04-03

    申请号:JP24848487

    申请日:1987-09-30

    Applicant: SHIMADZU CORP

    Abstract: PURPOSE:To enable the photodetection of the fluorescence in a 90 deg. direction where the Rayleigh scattering of excitation light is smallest by providing a migration gel and excitation light beam as well as a detector part, etc. CONSTITUTION:The excitation light beam 32 scanned in the direction orthogonal with the migration direction by a galvanomirror 34 escapes in the normal direction of the migration gel 2 at all the boundary faces with the gel 2 and, therefore, multireflections do not take place. Fluorescence is emitted from the nucleic acid fragments migrating in the gel 2 and propagates in the gel 2. The fluorescent light appearing at the end face of the gel 2 is detected 56 through light guides 50, 52 and an optical fiber bundle 54 and is converted to an electric signal. The signal indicating the projection position of the beam 32 onto the gel 2 from the rotating angle of the mirror 34 is taken into a signal processing part 58 which takes the fluorescent light in said position therein as the detection signal of a detector part 56. The development pattern of the DNA fragment specimen developed by electrophoresis in the gel 2 is obtd. as the fluorescent detection signal of the detector part 56 by scanning the entire surface of the gel 2 by the mirror 34 in such a manner. The direction where the fluorescent light is photodetected is 90 deg. with the beam 32 and the propagation of the Rayleigh scattering light is minimized.

    OPTICAL SCANNER
    8.
    发明专利

    公开(公告)号:JPS6456411A

    公开(公告)日:1989-03-03

    申请号:JP33167387

    申请日:1987-12-26

    Applicant: SHIMADZU CORP

    Abstract: PURPOSE:To simplify the structure of a reflecting optical system by fixing and placing a single optical scanner for scanning a light beam fro a light source, while reflecting it in a plane being orthogonal to the center axis of a rotary drum, and a photodetecting part of the light beam emitted from an optical scanner, in its opposed position, respectively. CONSTITUTION:When a rotary drum 2 is rotated in one direction, an optical scanner 16 and a photodetecting part 18 are also rotated, and the optical scanner scans a light beam from a light source 6, in a shape of a sector, while reflecting it in a plane being orthogonal to the center axis of the rotary drum 2, and the light beam emitted from the optical scanner 16 is photodetected by the photodetecting part 18. Accordingly, a reflected light path against the rotary drum 2 is fixed, but the light beam is scanned in a shape of a sector at a prescribed swing angle against a body to be inspected 4 so as to cover its measured area, and a radiated position of the light beam against the body to be inspected 4 is varied successively extending over the whole periphery at a prescribed pitch interval along the peripheral direction centering around the body to be inspected 4. In such a way, the structure of a reflecting optical system becomes simpler than usual.

    BASE SEQUENCE DETERMINING DEVICE
    9.
    发明专利

    公开(公告)号:JPS6435370A

    公开(公告)日:1989-02-06

    申请号:JP19316687

    申请日:1987-07-31

    Applicant: SHIMADZU CORP

    Abstract: PURPOSE:To uniformize the size and shape of an irradiation spot by reflecting the beam of the excitation light projected from the outside of a cylindrical electrophoresis gel by a reflecting mirror placed on the central axis of the electrophoresis gel. CONSTITUTION:The electrophoresis gel 2 is held in a cylindrical cell part 13. A laser 1 is provided on the outside of the gel 2 so that the beam 10 of the excitation light penetrates through the surface of the gel 2 so as to intersect orthogonally therewith and arrives at the plane mirror 3 placed on the inside axial center. The plane mirror 3 is reciprocatively rotated alternately forward and backward around the central axis of the gel 2 to project the laser beam over the required scanning range. Fluorescence is emitted when the laser beam falls onto the DNA band on the gel 2. Since this fluorescence is transmitted through the gel 2 to the end face by total reflection, the fluorescence is received by an optical fiber bundle 7 provided on the end face of the gel 2 and is guided through a filter 8 to a photoelectron multiplier 9.

    APPARATUS FOR DETERMINING BASE SEQUENCE

    公开(公告)号:JPS63206656A

    公开(公告)日:1988-08-25

    申请号:JP3948887

    申请日:1987-02-23

    Applicant: SHIMADZU CORP

    Abstract: PURPOSE:To make the reading of a migration pattern possible, by rotationally driving a gel itself with respect to exciting beam to irradiate while performing the electrophoresis of the gel. CONSTITUTION:At first, polyacrylamide gels 3a, 3b are formed to the gap between migration discs 1a, 1b to be solidified and, next, a specimen of a DNA fragment to be measured is charged from a large number of migration specimen charge ports. Thereafter, the migration discs are arranged so that the lower parts of the outer peripheries thereof are immersed in a cathode side electrolyte 7 and a cathode is put in a cathode side electrode tank 6 while a part becoming an electrolyte tank is filled with an anode side electrolyte and a current is supplied to start gel electrophoresis. At this time, the luminous flux from a laser beam 1 for an exciting beam is allowed to irradiate in the direction crossing the discs 1a, 1b at a right angle. When the DNA fragment is migrated to the irradiation point and a band reaches, the fluorescent dye preliminarily adhered to the terminal of the base sequence of the DNA fragment as a marker generates fluorescence which is, in turn, detected through a detector 10 and the signal at the time of detection is subsequently processed by a signal processing part 12 to perform actual reading operation.

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