Abstract: A first mode (one-knob off mode) and a second mode (one-knob on mode) are provided as modes for setting parameters. In the first mode, individual elements corresponding to respective parameters of a parameter set are displayed in an operable state, allowing setting of individual parameters. In the second mode, the individual elements are displayed in a non-operable state, and one-element is displayed in an operable state, and a plurality of parameters of the parameter set are controlled by operating the one-element. At the time of switching from the first mode to the second mode, the parameter set is initialized.

Abstract: Provided are a blood component measurement device and the like capable of further suppressing the errors in measuring blood components. A first current value that is generated by oxidation-reduction when a first voltage is applied to a first electrode pair 21, 22 composing a biosensor 1 is measured, a second current value that is generated when a second voltage is applied to a second electrode pair 23, 24 composing the biosensor 1 is measured, and then the first current and the second current are converted to give a blood component amount. Within a predetermined period after the introduction of blood into the biosensor 1, the first current is measured multiple times and the second current is measured once. A CPU 72 converts a plurality of first current values and the second current value to obtain a plurality of blood component amounts and calculates the blood component amount for the blood introduced into the biosensor 1 from said plurality of blood component amounts.

Abstract: It is intended to provide, for example, a liquid sample measurement device capable of measuring the amounts of components of a liquid with a high accuracy. A first voltage is applied to an electrode pair 21, 22, which composes a biosensor 1, to obtain, a first response value, a second voltage is applied to an electrode pair 23, 24, which composes the biosensor 1, to obtain a second response value, and a current that is generated when a third voltage is applied to an electrode pair 23, 27, which composes the biosensor 1, is detected to obtain a third response value. A liquid sample measurement device 6 uses the first response value, the second response value, and the third response value to obtain the concentration of glucose and the amount of blood cells of blood as well as the value equivalent to the temperature of the biosensor 1.

Abstract: A control object among control objects is assigned to each of a plurality of channel strips each have at least a control and are disposed on a panel according to a predetermined order. A parameter of control object assigned to each channel strip is adjusted in accordance with a manipulation of the control of the channel strip. A display unit is controlled to display parameters of the control objects assigned to a series of channel strips extracted from the channel strips arranged on the panel according to the order, and on accepting a first operation from the user, another series of channel strips are extracted from the channel strips, and the display unit is controlled to display parameters of the control objects assigned to the extracted channel strips.

Abstract: When a name of a group level control section is tapped, the group level control section is expanded and a group expansion screen is displayed on a display. In the group expansion screen, the group level control section is expanded and images of channel level control sections for respectively controlling output levels of channels belonging to a group corresponded to the group level control section are displayed by juxtaposing next to the group level control section. In this case, each channel level control section belongs to a lower layer than that of the group level control section. Although the channel level control sections and the group level control section belong to the different layers, they are aligned in the same line on the same screen on the display.

Abstract: Provided is a method for measuring a blood component amount that can sufficiently and properly correct the blood component amount by measuring an Hct value with high accuracy and high reliability, and a sensor and a measuring device that are used in the method. A method for measuring a blood component amount uses a biosensor to calculate a blood component amount in blood. The biosensor includes the following: a first electrode system having a first working electrode and a first counter electrode; a second electrode system having a second working electrode and a second counter electrode; and a reagent portion arranged in a form that covers at least a part of the first electrode system, but does not cover the second working electrode.

Abstract: Provided are a blood component measurement device and the like capable of further suppressing the errors in measuring blood components. A first current value that is generated by oxidation-reduction when a first voltage is applied to a first electrode pair 21, 22 composing a biosensor 1 is measured, a second current value that is generated when a second voltage is applied to a second electrode pair 23, 24 composing the biosensor 1 is measured, and then the first current and the second current are converted to give a blood component amount. Within a predetermined period after the introduction of blood into the biosensor 1, the first current is measured multiple times and the second current is measured once. A CPU 72 converts a plurality of first current values and the second current value to obtain a plurality of blood component amounts and calculates the blood component amount for the blood introduced into the biosensor 1 from said plurality of blood component amounts.

Abstract: Provided is a method for producing a plug for use in a piercing-rolling mill for producing a seamless steel tube/pipe, and the method for producing the plug for piercing-rolling comprises shotblasting a surface of the plug, and arc-spraying a spray wire so as to form a film on a surface of a base metal of the plug that is shotblasted. In the arc-spraying step, the arc spraying is carried out by using, as the spray wire, a cored wire whose iron sheath tube is charged with at least iron oxide particles among iron particles and the iron oxide particles (one or more of FeO particles, Fe3O4 particles, and Fe2O3 particles), so as to form the film containing iron oxide and Fe. Accordingly, it is possible to enhance the production efficiency of the plug, and to produce the plug for piercing-rolling capable of securing the steady enhancement of the durability life of the plug during the piercing-rolling.

Abstract: Provided is a blood component measuring device or the like that can further suppress the measurement error of a blood component. The device detects an oxidation-reduction current generated by oxidation-reduction when a first voltage is applied to a first electrode pair 21, 22 of a biosensor 1, and converts the oxidation-reduction current (glucose response value) into a glucose conversion value. The device detects a current generated when a second voltage is applied to a second electrode pair 23, 24 of the biosensor 1, and converts the detected current (blood cell amount response value) into a blood cell amount conversion value. The glucose response value is measured more than once and the blood cell amount response value is also measured more than once within a predetermined period after the introduction of the blood into the biosensor 1.

Abstract: Provided is an equipment system for producing a piercing-rolling plug to be used for producing a seamless steel tube/pipe, which includes a shotblasting device for applying shotblasting on a surface of the plug, and an arc-spraying device for performing arc-spraying of iron wires on a surface of a base metal of the plug to which the shotblasting is applied, so as to form a film containing oxide and Fe thereon. The arc-spraying device includes plural spraying booths each of which separately forms part of the film in turn in each of sections into which the surface of the base metal of the plug is divided along an axial direction of the plug. The production efficiency of the plug can therefore be maintained at a high level, and steady enhancement of the durability life of the plug can be realized during the piercing-rolling.

Abstract: When a disproportionated chlorosilane is to be produced by causing a starting material chlorosilane liquid to flow through a catalyst-packed layer which is packed with a weakly basic anion exchange resin as a disproportionation reaction catalyst to carry out a disproportionation reaction, before the disproportionation reaction is carried out, the disproportionation reaction catalyst is brought into contact with a processing gas obtained by diluting a chlorosilane with an inert gas to prevent the deterioration of the disproportionation reaction catalyst at the start of the reaction so as to carry out the disproportionation of the chlorosilane efficiently.

Abstract: Provided is a blood component measuring device or the like that can further suppress the measurement error of a blood component. The device detects an oxidation-reduction current generated by oxidation-reduction when a first voltage is applied to a first electrode pair 21, 22 of a biosensor 1, and converts the oxidation-reduction current (glucose response value) into a glucose conversion value. The device detects a current generated when a second voltage is applied to a second electrode pair 23, 24 of the biosensor 1, and converts the detected current (blood cell amount response value) into a blood cell amount conversion value. The glucose response value is measured more than once and the blood cell amount response value is also measured more than once within a predetermined period after the introduction of the blood into the biosensor 1.

Abstract: A melamine decorative laminated sheet has a melamine resin layer and a low refractive index layer which is formed upper than the melamine resin layer and has a lower refractive index than a refractive index of the melamine resin layer.

Abstract: Provided are a blood component measurement device and the like capable of further suppressing the errors in measuring blood components. A first current value that is generated by oxidation-reduction when a first voltage is applied to a first electrode pair 21, 22 composing a biosensor 1 is measured, a second current value that is generated when a second voltage is applied to a second electrode pair 23, 24 composing the biosensor 1 is measured, and then the first current and the second current are converted to give a blood component amount. Within a predetermined period after the introduction of blood into the biosensor 1, the first current is measured multiple times and the second current is measured once. A CPU 72 converts a plurality of first current values and the second current value to obtain a plurality of blood component amounts and calculates the blood component amount for the blood introduced into the biosensor 1 from said plurality of blood component amounts.

Abstract: In a group level control section, a largest output level among those in channels belonging to a relevant group is selected automatically as a group level. By operating a control part of a channel level control section displayed on a basic screen, an output level of an input channel corresponding to the operated channel level control section can be controlled. Further, by operating a control part of a group level control section, output levels of the input channels belonging to the group can be collectively controlled with difference in levels among the input channels being maintained.

Abstract: It is an object of the present invention to provide a mutant streptavidin with a reduced affinity for natural biotin, and also to provide a modified biotin having a high affinity for the mutant streptavidin with a reduced affinity for natural biotin. According to the present invention, there is provided a reagent kit for use in treatments or diagnoses, which comprises: (a) a mutant streptavidin with a reduced affinity for natural biotin or biocytin; and a modified biotin having a high affinity for the above-described mutant streptavidin.

Abstract: A control object among control objects is assigned to each of a plurality of channel strips each have at least a control and are disposed on a panel according to a predetermined order. A parameter of control object assigned to each channel strip is adjusted in accordance with a manipulation of the control of the channel strip. A display unit is controlled to display parameters of the control objects assigned to a series of channel strips extracted from the channel strips arranged on the panel according to the order, and on accepting a first operation from the user, another series of channel strips are extracted from the channel strips, and the display unit is controlled to display parameters of the control objects assigned to the extracted channel strips.

Abstract: A first mode (one-knob off mode) and a second mode (one-knob on mode) are provided as modes for setting parameters. In the first mode, individual elements corresponding to respective parameters of a parameter set are displayed in an operable state, allowing setting of individual parameters. In the second mode, the individual elements are displayed in a non-operable state, and one-element is displayed in an operable state, and a plurality of parameters of the parameter set are controlled by operating the one-element. At the time of switching from the first mode to the second mode, the parameter set is initialized.

Abstract: In a group level control section, a largest output level among those in channels belonging to a relevant group is selected automatically as a group level. By operating a control part of a channel level control section displayed on a basic screen, an output level of an input channel corresponding to the operated channel level control section can be controlled. Further, by operating a control part of a group level control section, output levels of the input channels belonging to the group can be collectively controlled with difference in levels among the input channels being maintained.

Abstract: When a name of a group level control section is tapped, the group level control section is expanded and a group expansion screen is displayed on a display. In the group expansion screen, the group level control section is expanded and images of channel level control sections for respectively controlling output levels of channels belonging to a group corresponded to the group level control section are displayed by juxtaposing next to the group level control section. In this case, each channel level control section belongs to a lower layer than that of the group level control section. Although the channel level control sections and the group level control section belong to the different layers, they are aligned in the same line on the same screen on the display.