Abstract: A modified pyrroloquinoline quinone glucose dehydrogenase that exhibits a high selectivity for glucose is provided. A modified pyrroloquinoline quinone glucose dehydrogenase is disclosed in which the amino acid residue G at Position 99 of a pyrroloquinoline quinone glucose dehydrogenase (PQQGDH) represented by SEQ ID NO: 1, or the amino acid residue G at Position 100 of the pyrroloquinoline quinone glucose dehydrogenase (PQQGDH) represented by SEQ ID NO: 3, is substituted by the amino acid sequence TGZN (where Z is SX, S, or N and X is any amino acid residue). The modified PQQGDH of the present invention may additionally comprise one or more mutations selected from the group consisting of Q192G, Q192A, or Q192S; L193X; E277X; A318X; Y367A, Y367F, or Y367W; G451C; and N452X (where X is any amino acid residue).

Abstract: The present invention relates to a method for purifying target protein which contains electron transfer protein, from a protein solution containing the target protein, by means of liquid chromatography. The liquid chromatography is performed as follows: First, the protein solution is introduced into a column which is filled with a packing agent, thereby causing the packing agent to bond to the target protein. Then, impurities are removed, and then the target protein is eluted from the packing agent in an eluent which contains a hydroxy-cholate. An example of the target protein is glucose dehydrogenase which contains a protein having glucose dehydrogenation activity. The liquid chromatography is performed as a combination of hydrophobic chromatography and anion exchange chromatography.

Abstract: The present invention relates to an attachment (X) for body fluid sampling device, comprising: a lancing member (21) including a lancing needle (28); an analyzing implement (5) for obtaining information on a target component in body fluid; and an attachment main body (1) holding the lancing member (21) and the analyzing implement (5). The attachment main body (X) includes a movable member (3) movable with the analyzing implement (5) longitudinally of the lancing needle (28). The attachment main body (1) includes for example, a holder (2) for holding the lancing member (21). The holder (2) has an inner space (22) for movement of the lancing needle (28). The lancing needle (28) is held preferably as sealed in the inner space (22).

Abstract: A sample detector B includes a member 6 provided with an aperture 60, as well as a light receiving element 5 which receives two light beams directed from a pair of light sources 40, 41 to a detection area AR and having passed through the detection area and outputs a signal corresponding to the amount of light received, and a determination means 8 for determining whether or not a sample is properly supplied to the detection area AR based on the signal. Two light beams emitted from the paired light sources 40, 41 travel through paths defined by the aperture 60 to regions ARr, ARf of the detection area AR which are positionally deviated from each other. With this arrangement, whether or not a sample is properly supplied to the detection area AR is precisely determined without using an expensive component such as an optical lens.

Abstract: By moving a control member 3 in a predetermined direction from a wait position, a lancing device A can perform a lancet retreat operation for retreating a lancet holder 2 to locate a lancet 9 at a predetermined retreated position and a lancet detachment operation for pushing out the lancet 9 forward of the lancet holder 2 after a lancing operation. The control member 3 returns to the wait position by action of a return member 7 both after the lancet retreat operation and after the lancet detachment operation. Thus, the lancing device A is convenient.

Abstract: The present invention provides a dry reagent capable of amplifying a nucleic acid even after being stored in a dry state at room temperature, a dry reagent kit, a reagent container, and a method for producing the dry reagent and methods of producing and using thereof.

Abstract: The present invention relates to a cartridge 1 including a plurality of analyzing tools 3 arranged lined in a plane direction and a case 2 for accommodating the plurality of analyzing tools 3, and being configured to take out the analyzing tool 3 one at a time from the case 2. The plurality of analyzing tools 3 further include engagement means 32, 33 for restricting the analyzing tools 3 adjacent to each other in the plane direction and allowing removable attachment in a thickness direction D1, D2 of the analyzing tool 3. The present invention further relates to an analyzer and an analyzing system for analyzing a sample using the cartridge 1.

Abstract: The invention relates to a measurement system MS1 provided with a plurality of loading units 10 into which a measurement tool 4 supporting a reagent is loaded. The measurement system MS1 includes reading means 2 for reading information on an analyte provider that includes identification information, and guidance means 11 for guiding the measurement tool 4 to which an analyte derived from the analyte provider has been or is to be applied, to a loading unit that is selected from the plurality of loading units 10 and individually associated with the analyte provider based on the identification information that has been read by the reading means 2. With such configuration, the measurement results obtained from the analyte derived from the analyte provider can be easily associated with the information on the analyte provider that includes the identification information.

Abstract: The present invention relates to a puncture device 1 for moving a puncture element 21 in a piercing direction N1 and for piercing a target site with the puncture element 21. The puncture device 1 is for moving a second member 42 retaining the puncture element 21 in the direction N1 and in a direction N2 by the rotational motion of a third member 40 as a first member 41 moves in the directions N1 and N2. The puncture device 1 further comprises a piercing depth adjusting mechanism 6 of adjusting a piercing depth of the puncture element 21 to the target site by regulating a rotation angle of the third member 40.

Abstract: A technique is provided, which makes it possible to continuously supply the driving electric power stably to a sensor even when the continuous monitoring period ranges over a long period of time when the numerical information is measured in relation to a test substance contained in a sample.

Abstract: This invention relates to technology for analyzing a specific component in a sample liquid, and provides an analyzing tool and an analyzing apparatus. Analyzing tool (Y) includes a liquid inlet (61) at a central portion of the tool and a plurality of channels (51) which communicate with liquid inlet (61) and move the sample liquid introduced through liquid inlet (61) by capillary action from the central portion towards a peripheral portion of the tool. Each channel (51) extends linearly for example from the central portion towards the peripheral portion, and the plurality of channels (51) are arranged radially.

Abstract: The present invention relates to a method for automatically discriminating a control solution from a sample in a measurement system for measuring a target ingredient in the sample by using a measurement wavelength and a reference wavelength, wherein as the control solution, a control solution having a response value lower than a lower limit value (threshold) of a response value, such as absorbance, supposed when luminance of the sample is measured at the reference wavelength and having a response value higher than an upper limit value (threshold) of a response value supposed when luminance of the sample is measured at the detection wavelength for detecting whether the sample is supplied is used.

Abstract: The present invention provides an amplification determining method that can determine whether or not an objective nucleic acid has been amplified with respect to a sample treated so as to amplify the nucleic acid. Signal values showing molten states of the treated sample at respective temperatures are provided, and the maximum signal value (A) is searched for. Further, signal differential values at the respective temperatures are calculated by differentiation of the signal values at two successive points, and second-order differential values of the differential values are calculated by differentiation at four successive points. Among the second differential values, from those in a predetermined temperature range including a Tm value of the objective nucleic acid, the maximum second differential value (Dmax?) and the minimum second differential value (Dmin?) are selected. Then, the maximum difference (B) is calculated based on the formula (B)=(Dmax?)?(Dmin?).

Abstract: A method for measuring LDL cholesterol in a sample using a test piece is provided which involves a step of measuring the total cholesterol in the sample; a step of measuring the non-LDL cholesterol in the sample; and a step of subtracting the non-LDL cholesterol value from the total-cholesterol value to obtain the LDL cholesterol level.

Abstract: A measuring device in a monitoring system including a monitoring device for monitoring data received via a network is provided. The measuring device includes a measurer for measuring the data, a data transmitter for sending the data to a communication device that performs communication with the monitoring device, a forbidding condition determiner for determining whether or not a predetermined forbidding condition is satisfied, and a transmission forbidder for forbidding transmission of the data to the communication device or to the monitoring device when the forbidding condition determiner determines that the predetermined forbidding condition is satisfied.

Abstract: A dry test strip for measuring calcium is comprising a support, a reagent layer provided on the support, and a reagent holding layer provided on the reagent layer, and containing, as reagents, o-cresolphthalene complexone, a magnesium selective masking agent, and a pH buffer for adjusting the pH of the environment for reaction of the o-cresolphthalene complexone with calcium to 10.0-11.0, wherein such reagents are present in either the reagent layer or the reagent holding layer or the both layers.

Abstract: A blood sugar level control system for measuring a blood sugar level and administering insulin into a body. The blood sugar level control system includes a blood sugar measuring device having a first wireless data transmitting part to transmit data relating to the blood sugar level; an insulin dispensing device having a wireless data communication unit including a second wireless data transmitting part to transmit data to a second blood sugar measuring device, and a wireless data receiving part to receive data from the first wireless data transmitting part and the second blood sugar measuring device; and an attachment mechanism to couple the insulin dispensing device and the blood sugar measuring device so that the blood sugar measuring device is movable, without separating from the insulin dispensing device at least three specific positions.

Abstract: The present invention provides a method of pretreating a sample containing a glycated amine as an analyte, thereby enabling highly reliable measurement of a glycated amine. A glycated amino acid in the sample is degraded by causing a fructosyl amino acid oxidase (FAOD) to act thereon, and thereafter, a FAOD further is caused to act on the glycated amine as the analyte in the sample to cause a redox reaction. The amount of the glycated amine is determined by measuring the redox reaction. The substrate specificity of the FAOD caused to act on the glycated amino acid may be either the same as or different from that of the FAOD caused to act on the glycated amine. When using the same FAOD, a FAOD is caused to act on the glycated amino acid to degrade it, and thereafter, the sample is treated with a protease to inactivate the FAOD and also to degrade the glycated amine.