Sekisui Kagaku Kogyo Kabushiki Kaisha

Sekisui Chemical Co., Ltd.

Japan Immunoresearch Laboratories Co., Ltd.

Sekisui Kagaku Kogyo K.k.

Japan Immuno Research Lab. Co., Ltd. of Gunma, Japan

Sekisui Kagaku Kogyo Kabushiki Kaisha of Osaka, Japan

Kazutoshi Yamazaki

Masahiro Takechi

Toshiki Kawabe

Masayuki Yokoi

Kazuo Shinmura

Yoshiko Abe

Masakazu Adachi

Fumio Kamiyama

Minoru Kohara

Kozo Shirato

Kazuyasu Kawashima

Akihiko Nagai

Mituo Nagata

Akira Sato

Hideo Matsumura

Hirohito Nishino

Hidetoshi Fukuyama

Hiromitsu Suzuki

Kazuyuki Oishi

Makoto Takahara

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

Ozone treating apparatus

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.

Granulocyte adsorbing carrier and granulocyte remover

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.

Method of forming a granulocyte adsorbing carrier and granulocyte remover

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.

Eliminating agent for glycosylated hemoglobin and a test method using

Method for producing a carrier for cation exchange liquid chromatography

Method of treating blood containing labile glycosylated hemoglobin

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 said cell block by means of said gasket while said supporter and said cell unit are being incorporated into one piece, which removes the pressure from said pressure means.

Electrochemical detection device

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.

Filler for liquid chromatography and method for separating water-soluble

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Ohtsu, Japan

Kazutoshi Yamazaki