Abstract: Methods and systems of evaluating a performance of an entity are described. A processor may obtain first data indicating tier attributes of resources of the entity, second data indicating function attributes of the resources, and third data indicating productivity attributes of the resources. The processor may train a model based on the first data, the second data, and the third data, the model may represent transitions of the resources over time. The processor may receive a set of controls including at least an objective to optimize a performance of the entity. The processor may generate a controlled model by integrating the set of controls into the model. The processor may determine a set of outcomes from the controlled model that includes at least a set of transitions relating to the resources that may optimize the performance of the entity.

Abstract: Methods and systems of evaluating a performance of an entity are described. A processor may obtain first data indicating tier attributes of resources of the entity, second data indicating function attributes of the resources, and third data indicating productivity attributes of the resources. The processor may train a model based on the first data, the second data, and the third data, the model may represent transitions of the resources over time. The processor may receive a set of controls including at least an objective to optimize a performance of the entity. The processor may generate a controlled model by integrating the set of controls into the model. The processor may determine a set of outcomes from the controlled model that includes at least a set of transitions relating to the resources that may optimize the performance of the entity.

Abstract: To provide an antiseptics, a detergent, an antimicrobial, a deodorizer against nitrogenous odor, an insecticide, a repellent and a bactericide, containing an ozonized surfactant obtained by adding ozone to a surfactant having at least one olefin-based double bond in a hydrophobic group moiety. These are highly safe to the human body and have features and performance that ordinary surfactants do not have.

Abstract: Disclosed herein is an ozonized surfactant which has the same level of bactericidal and deodorizing abilities as that of ozonized olive oil and which can be evenly applied or sprayed onto and can permeate any place or environment (a highly hydrophilic or hydrophobic place or environment). The ozonized surfactant can be obtained by adding ozone to a surfactant having at least one olefin-based double bond in a hydrophobic group moiety.

Abstract: The present invention provides an ozonization apparatus which is not only capable of dissolving ozone in material water with high efficiency and speedily but also enables the easy and proper control of the dissolved ozone concentration of ozone water. The present invention relates to an ozonization apparatus comprising an ozone gas-permeable membrane disposed to isolate material water and ozone gas from each other and allow said ozone gas to be dissolved in said material water by permeation, said ozone gas-permeable membrane being a nonporous hollow tube which is selectively gas-permeable and liquid-impermeable.

Abstract: The present invention provides an ozonization apparatus which is not only capable of dissolving ozone in material water with high efficiency and speedily but also enables the easy and proper control of the dissolved ozone concentration of ozone water.

Abstract: A plurality of light emitting units are prepared each of which is provided with a laser diode having a laser diode chip which emits one beam and a collimator lens for converting a beam emitted from the laser diode into a parallel beam. The light emitting units are fixed to a bar body so as to be in a row. A plurality of such bar bodies are prepared, and by fixing the bar bodies to a substrate, the light source units are arranged in a matrix form. The positions of the light emitting units are adjusted and fixed after the light emitting units are fitted in the bar bodies so that a plurality of beams emitted from the laser diodes are in parallel with one another at predetermined intervals.

Abstract: A plurality of light emitting units are prepared each of which is provided with a laser diode having a laser diode chip which emits one beam and a collimator lens for converting a beam emitted from the laser diode into a parallel beam. The light emitting units are fixed to a bar body so as to be in a row. A plurality of such bar bodies are prepared, and by fixing the bar bodies to a substrate, the light source units are arranged in a matrix form. The positions of the light emitting units are adjusted and fixed after the light emitting units are fitted in the bar bodies so that a plurality of beams emitted from the laser diodes are in parallel with one another at predetermined intervals.

Abstract: Disclosed herein are a granulocyte adsorbing carrier which is provided on its surface with irregularities having a center line average height Ra of 0.2 to 10 .mu.m and a mean spacing Sm of unevenness being within a range of 5 to 200 .mu.m, and a granulocyte remover employing the granulocyte adsorbing carrier.

Abstract: A method of making a granulocyte adsorbing carrier, which is provided on its surface with irregularities having a center line average height Ra of 0.2 to 10 .mu.m and a mean spacing Sm of unevenness being within a range of 5 to 200 .mu.m, and a granulocyte remover employing the granulocyte adsorbing carrier, is conducted by methanol extraction.

Abstract: An eliminating agent used for the measurement of the amount of glycosylated hemoglobins in a blood sample is provided. The eliminating agent comprises condensed phosphoric acids and/or the salts thereof as the main ingredient, wherein the agent eliminates labile glycosylated hemoglobin A.sub.1c into non-glycosylated hemoglobin and glucose. There is also provided a reagent comprising the eliminating agent and a hemolysis agent, which is used for the measurement of the amount of glycosylated hemoglobins; and an eluent comprising the eliminating agent, which is used for the separation of glycosylated hemoglobins in blood samples by ion-exchange chromatography to measure the amount of the glycosylated hemoglobins. A method for measuring the amount of glycosylated hemoglobin A.sub.1c in a blood sample involves the use of the eliminating agent, the reagent comprising the eliminating agent and the hemolysis agent, and/or the eluent.

Abstract: A semiconductor laser is inserted into a first hole of a fixing member. An optical system including a cylindrical lens barrel and a lens attached inside the lens barrel is inserted into a second hole in order to direct a light beam emitted from the semiconductor laser to a predetermined position. The first and second holes are formed to be opposite to each other and are arranged on the same axis. The semiconductor laser and the optical system inserted into the first and second holes, respectively, so as to be partly exposed are fixed by laser welding at entrances of the first and second holes. The fixing member is provided with a third hole vertically penetrating the second hole. An adhesive is filled into the third hole. Further, an adhesive is applied onto laser welding points at the entrance of the first hole.

Abstract: An eliminating agent used for the measurement of the amount of glycosylated hemoglobins in a blood sample is provided. The eliminating agent comprises condensed phosphoric acids and/or the salts thereof as the main ingredient, wherein the agent eliminates labile glycosylated hemoglobin A.sub.1c into non-glycosylated hemoglobin and glucose. There is also provided a reagent comprising the eliminating agent and a hemolysis agent, which is used for the measurement of the amount of glycosylated hemoglobins; and an eluent comprising the eliminating agent, which is used for the separation of glycosylated hemoglobins in blood samples by ion-exchange chromatography to measure the amount of the glycosylated hemoglobins. A method for measuring the amount of glycosylated hemoglobin A.sub.1c in a blood sample involves the use of the eliminating agent, the reagent comprising the eliminating agent and the hemolysis agent, and/or the eluent.

Abstract: According to the present invention, a production method of a carrier appropriate for cation exchange liquid chromatography and a method for determining glycosylated hemoglobins using the carrier obtained by the production method are provided.The production method of the carrier comprises the steps of providing hydrophobic particles to which a polymerization initiator is adhered; and adding a polymerizable monomer having a carboxyl group to an aqueous dispersion in which the hydrophobic crosslinked polymer particles are dispersed and polymerizing the monomer on surfaces of the hydrophobic crosslinked polymer particles, thereby obtaining polymer particles the surfaces of which are coated with polymer layers having carboxyl groups.

Abstract: An electrochemical detection device comprising a cell unit that has a cell therein and a supporter that rotatably supports said cell unit and that is made in one piece with said cell unit, wherein said cell unit has a cell block that has a test solution introduction route through which a test solution flows after being introduced into the inside of said cell block and that has a test solution outlet route through which the test solution leaves the inside and that has a reference electrode and a counter electrode provided so that they come into contact with the test solution flowing from said test solution introduction route to said test solution outlet route; a gasket that has an opening constituting said cell, and that is in contact with said cell block so that said opening is connected with both the test solution introduction route and the test solution outlet route; a working electrode that faces said opening of the gasket, and said supporter has a pressure means that pushes said working electrode onto sai

Abstract: A liquid-chromatographic filler comprising a particulate synthetic polymer, such as glycerol di or tri (meth) acrylate wherein the filler exhibits a behavior such that in chromatography using polyethylene glycol as a sample and water as an eluent, the elution time of the sample increases with a rise in temperature. Separation of water-soluble substances by liquid chromatography can be achieved by using an aqueous medium as an eluent, and this filler.