`In Reply to Office Action mailed: January 5, 2017
`
`Amendments to the Claims:
`
`This listing of claims will replace all prior versions, and listing, of claims in the
`
`application.
`
`l.-l4.
`
`(Canceled)
`
`15.
`
`(Previously Presented) An analysis device, comprising:
`
`a microchannel structure rotatable about a rotation axis of the analysis device, the
`
`microchannel structure including a passage and a measuring cell; and
`
`an analysis reagent carried in the passage of the microchannel structure, the
`
`analysis reagent being in a solid and dry state, the analysis reagent comprising a
`
`combination of a polyanionic compound and a bivalent cationic compound, and one
`
`substance or one compound of the substance as an additive,
`
`wherein the substance is at least one selected from the group consisting of:
`
`succinic acid,
`
`gluconic acid,
`
`valine,
`
`histidine, and
`
`maltitol.
`
`l6.
`
`(Withdrawn) An analysis device, comprising:
`
`a microchannel structure rotatable about a rotation axis of the analysis device, the
`
`microchannel structure including a passage and a measuring cell;
`
`an analysis reagent carried in the passage of the microchannel structure, the
`
`analysis reagent being in a solid and dry state, the analysis reagent comprising a
`
`combination of a polyanionic compound and a bivalent cationic compound, and one
`
`substance or one compound of the substance as an additive,
`
`wherein the substance is at least one selected from the group consisting of:
`
`dicarboxylic acid,
`
`gluconic acid,
`
`
`
`S/N: 14/479,936
`In Reply to Office Action mailed: January 5, 2017
`
`valine,
`
`histidine,
`
`taurine,
`
`a sugar alcohol,
`
`xylose that is a monosaccharide,
`
`a disaccharide, and
`
`a trisaccharide.
`
`17.
`
`(Previously Presented) The analysis device according to claim 15, comprising:
`
`a reserving cavity that receives a fixed quantity of diluted plasma serving as a
`
`liquid sample;
`
`an operation cavity that is formed next to the reserving cavity in a circumferential
`
`direction, is connected to the reserving cavity via a connecting section enabling
`
`application
`
`of a capillary force, and contains a reagent for analyzing highdensity lipoprotein
`
`cholesterol,
`
`a separating cavity that is formed outside the operation cavity and is connected to
`
`the operation cavity via a connecting passage serving as a clearance configured to apply a
`
`capillary force;
`
`a measuring passage that is adjacent to the separating cavity in the
`
`circumferential direction and is connected to the separating cavity via a connecting
`
`passage configured to apply a capillary force,
`
`a measuring cell formed outside the measuring passage; and
`
`a capillary area that is formed inside the measuring cell and contains an enzyme
`
`reagent and a mediator,
`
`wherein a reaction solution having reacted in the capillary area is transferred to an
`
`outer periphery of the measuring cell by increasing the centrifugal force, and then the
`
`reaction solution retained on the outer periphery of the measuring cell is accessed to
`
`measure HDL of the liquid sample.
`
`
`
`S/N: 14/479,936
`In Reply to Office Action mailed: January 5, 2017
`
`18 .
`
`(Previously Presented) The analysis device according to claim 17, wherein the
`
`operation cavity comprises a reagent carrying section configured to carry the reagent for
`
`analyzing high-density lipoprotein cholesterol, the reagent carrying section protruding
`
`from the operation cavity so as to have a clearance smaller than a clearance of the
`
`operation cavity.
`
`19.
`
`(Previously Presented) The analysis device according to claim 17, further
`
`comprising an agitating rib extended in a radial direction in the operation cavity, the
`
`agitating rib being lower in height than an external wall of the operation cavity.
`
`20.
`
`(Previously Presented) The analysis device according to claim 15, wherein the
`
`substance is at least one selected from the group consisting of:
`
`succinate at a concentration of at least 5 mg/ml,
`
`gluconate at a concentration of at least 5 mg/ml,
`
`valine at a concentration of at least 5 mg/ml,
`
`histidine at a concentration of at least 5 mg/ml,
`
`histidine at a concentration of at least 5 mg/ml, and
`
`maltitol at a concentration of 1 mg/ml to 10 mg/ml.
`
`21.
`
`(Previously Presented) The analysis device according to claim 15, wherein the
`
`substance is succinic acid.
`
`22.
`
`(Previously Presented) The analysis device according to claim 21, wherein the
`
`succinic acid is succinate at a concentration of at least 5 mg/ml.
`
`23.
`
`(New) The analysis device according to claim 15, wherein the analysis reagent
`
`further comprises calcium sulfate, and
`
`the bivalent cationic compound is at least one selected from the group consisting
`
`of:
`
`magnesium ion compound; and
`
`magnesium ion compound salt.
`
`
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