Abstract: A pipette tip includes a body and projections. In the body, a flow passage in which liquid from the syringe flows and an ejection opening that ejects the liquid, which has flowed through the flow passage, to the outside are formed. The ejection opening is formed in a distal end portion. The projections are provided on the distal end portion and protrude from a region around the ejection opening in the ejection direction of liquid. The projections are partially disposed around the central axis of the body. Even in a case where a residual droplet adheres to the ejection opening, the residual droplet does not adhere to an injection opening of a sample container, because the projections guard a region around the residual droplet.

Abstract: A storage portion forming a storage space 10, includes an inclined inner wall portion 20 that is connected to a base portion so that the diameter of the inclined inner wall portion gradually decreases; a concave portion 22 is formed at a part of the inclined inner wall portion; and the concave portion 22 includes a concave portion side surface 22b that is connected to a concave portion bottom surface 22a. The concave portion 22 is formed at a position, where the concave portion crosses an interface S between the specimen centrifuged during rotation and air, in a radial direction with respect to the central axis; and the maximum width of the concave portion 22 in a circumferential direction around the central axis is included in a range of 2 mm to a length of 20% of the whole circumference.

Abstract: A centrifugal separation unit that performs centrifugal separation on a sample that has been injected into a container by rotating the container about a center axis of the container, as a rotation axis, a measurement unit that measures a sample component in the container that has been centrifugally separated by the centrifugal separation unit, and a correction unit that performs, on a result of the measurement, correction operation processing based on a change in concentration caused by evaporation of the sample during the centrifugal separation are provided.

Abstract: In a container for centrifugal separation that includes a container main body including a retention part in which a sample is retained, and in which a component of the sample in the retention part is centrifugally separated by rotating the container main body about its center axis, as a rotation axis, material having thixotropic properties has been applied to an entire bottom surface of the retention part.

Abstract: A pipette tip includes a body and projections. In the body, a flow passage in which liquid from the syringe flows and an ejection opening that ejects the liquid, which has flowed through the flow passage, to the outside are formed. The ejection opening is formed in a distal end portion. The projections are provided on the distal end portion and protrude from a region around the ejection opening in the ejection direction of liquid. The projections are partially disposed around the central axis of the body. Even in a case where a residual droplet adheres to the ejection opening, the residual droplet does not adhere to an injection opening of a sample container, because the projections guard a region around the residual droplet.

Abstract: A storage portion forming a storage space 10, includes an inclined inner wall portion 20 that is connected to a base portion so that the diameter of the inclined inner wall portion gradually decreases; a concave portion 22 is formed at a part of the inclined inner wall portion; and the concave portion 22 includes a concave portion side surface 22b that is connected to a concave portion bottom surface 22a. The concave portion 22 is formed at a position, where the concave portion crosses an interface S between the specimen centrifuged during rotation and air, in a radial direction with respect to the central axis; and the maximum width of the concave portion 22 in a circumferential direction around the central axis is included in a range of 2 mm to a length of 20% of the whole circumference.

Abstract: A centrifugal separation unit that performs centrifugal separation on a sample that has been injected into a container by rotating the container about a center axis of the container, as a rotation axis, a measurement unit that measures a sample component in the container that has been centrifugally separated by the centrifugal separation unit, and a correction unit that performs, on a result of the measurement, correction operation processing based on a change in concentration caused by evaporation of the sample during the centrifugal separation are provided.

Abstract: In a container for centrifugal separation that includes a container main body including a retention part in which a sample is retained, and in which a component of the sample in the retention part is centrifugally separated by rotating the container main body about its center axis, as a rotation axis, material having thixotropic properties has been applied to an entire bottom surface of the retention part.

Abstract: Judgment as to whether an analyte is present is performed before a washing step in which a washing liquid for washing a test area and the vicinity of the test area is supplied to a test strip. If the analyte is detected, the judgment ends, but if the analyte is not detected, judgment is performed again after the test area and the vicinity of the test area are washed.

Abstract: There is provided an adapter for blood sample dispensing which enables change of the presence and absence of a medicine to be mixed in a blood sample or the type of the medicine thereof while suppressing contact of blood with the air, during preparation of an examination sample, and a dispensing kit and a needle kit provided therewith. Dispensing is performed using an adapter 1 for blood sample dispensing which is mounted on a distal portion of a syringe and has a piping structure, in which the adapter has a fitting portion 3 fitted to the distal portion at one end, a nozzle portion 2 at the other end, and a flange portion 4 on an outer circumference surface, and in which the adapter 1 has a medicine 5, to be mixed in the blood sample S, on the inside of the nozzle portion 2.

Abstract: A storage portion forming a storage space 10, includes an inclined inner wall portion 20 that is connected to a base portion so that the diameter of the inclined inner wall portion gradually decreases; a concave portion 22 is formed at a part of the inclined inner wall portion; and the concave portion 22 includes a concave portion side surface 22b that is connected to a concave portion bottom surface 22a. The concave portion 22 is formed at a position, where the concave portion crosses an interface S between the specimen centrifuged during rotation and air, in a radial direction with respect to the central axis; and the maximum width of the concave portion 22 in a circumferential direction around the central axis is included in a range of 2 mm to a length of 20% of the whole circumference.

Abstract: Judgment as to whether an analyte is present is performed before a washing step in which a washing liquid for washing a test area and the vicinity of the test area is supplied to a test strip. If the analyte is detected, the judgment ends, but if the analyte is not detected, judgment is performed again after the test area and the vicinity of the test area are washed.

Abstract: In a method for testing a patient with a test apparatus for a plurality of diseases using a specimen collected from the subject, if the subject is determined to be positive for one of the plurality of diseases, a test result indicating the positive is outputted from the test apparatus without waiting for completion of the testing of the other diseases.

Abstract: A chromatographic measurement apparatus for measuring a color development state of an insoluble carrier with a sample solution and a label solution developed thereon to test a test article, the insoluble carrier including a test detection area where a material that binds specifically to a test article is immobilized and a control detection area used for determining an end of measurement. The chromatographic measurement apparatus includes: a determining unit for carrying out determination of validity and determination of necessity of amplification of a test result of the test article; and an amplifying unit for amplifying the color development state according to the result of the determination of necessity of amplification by the determining unit. The amplification is carried out only when it is determined that amplification is necessary.

Abstract: A method is provided which is capable of efficiently taking most of a precious sample into an extraction vessel without wasting when the sample is extracted from a collection section of a sampling rod. The method includes the steps of collecting a sample using a sampling rod formed of a rod body and a collection section attached to the rod body, inserting the sampling rod into the extraction vessel, placing the rod body in a gap formed in a grappling hook section which is disposed in an insertion path of the sampling rod, the gap having a width smaller than a diameter of the collection section and being capable of receiving the rod body, withdrawing the rod body with the rod body being placed in the gap and detaching the collection section from the rod body by hooking the collection section to the grappling hook section.

Abstract: A method is provided which is capable of efficiently taking most of a precious sample into an extraction vessel without wasting when the sample is extracted from a collection section of a sampling rod. The method includes the steps of collecting a sample using a sampling rod formed of a rod body and a collection section attached to the rod body, inserting the sampling rod into the extraction vessel, placing the rod body in a gap formed in a grappling hook section which is disposed in an insertion path of the sampling rod, the gap having a width smaller than a diameter of the collection section and being capable of receiving the rod body, withdrawing the rod body with the rod body being placed in the gap and detaching the collection section from the rod body by hooking the collection section to the grappling hook section.

Abstract: A coloration state of a test region is read out as image density values by a readout device. A calculation is made to find a similarity degree between template information for the test region, which template information represents a state of coloration of the test region, and which has been stored previously in a pattern storing device, and the coloration state of the test region, which coloration state has been read out by the readout device. An analysis of an analyte is performed by a judgment device in accordance with the similarity degree, which has been calculated.

Abstract: Testing of a test article based on a color development state of a test area is achieved in an easy manner. A sample is deposited on a spreading layer of a test piece, and the test piece is loaded in a loading port of a chromatographic analysis apparatus. After a preset time has elapsed, color development states of the test area and a control area in an observation window are read as an image. A preprocessing unit applies preprocessing to the image, and then, spatial frequency components of the image are calculated. Then, pattern information is generated based on the spatial frequency components, and the pattern information is displayed on an information output unit.

Abstract: A chromatographic measurement apparatus for measuring a color development state of an insoluble carrier with a sample solution and a label solution developed thereon to test a test article, the insoluble carrier including a test detection area where a material that binds specifically to a test article is immobilized and a control detection area used for determining an end of measurement. The chromatographic measurement apparatus includes: a determining unit for carrying out determination of validity and determination of necessity of amplification of a test result of the test article; and an amplifying unit for amplifying the color development state according to the result of the determination of necessity of amplification by the determining unit. The amplification is carried out only when it is determined that amplification is necessary.

Abstract: The image processing apparatus includes an image processing section for executing at least one image processing operation with respect to digital image data and a set value chancing device for selecting a plurality of image processing conditions as to said at least one image processing operation from among plural levels or plural combinations which are typically preset of image processing conditions, and changing set values of the plurality of image processing conditions from previously set values into the selected plurality of image processing conditions. The customized printing system includes the image processing apparatus, an image input apparatus and an image output apparatus. The image processing apparatus is capable of executing the image processing operation or operations in response to a printing order customized by a customer, and the system is capable of forming a print which may reflect the requests from the customer.