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An analysis device includes: a separation cavity 18 for separating a test liquid into a solution component and a solid component by using a centrifugal force; a higher specific gravity component quantitative cavity 23 for holding a portion of the separated solid component which has been transferred;

An analysis device includes: a separation cavity 18 for separating a test liquid into a solution component and a solid component by using a centrifugal force; a higher specific gravity component quantitative cavity 23 for holding a portion of the separated solid component which has been transferred; a sample solution overflow cavity 22 arranged between the higher specific gravity component quantitative cavity 23 and the separation cavity 18 and connected to a connecting channel 21 for transporting the sample liquid from the separation cavity 18; and a capillary cavity 19 formed in the separation cavity 18 for temporarily holding a separated solution component (blood plasma) in the separation cavity 18. A blood plasma component 57a remaining in the separation cavity 18 is trapped by the capillary cavity 19.

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1. An analysis method using an analysis device having a microchannel structure that transfers a sample liquid towards a measurement spot by centrifugal force generated by rotating the analysis device about a rotation center and which is used to read a reactant at the measurement spot, the analysis m

1. An analysis method using an analysis device having a microchannel structure that transfers a sample liquid towards a measurement spot by centrifugal force generated by rotating the analysis device about a rotation center and which is used to read a reactant at the measurement spot, the analysis method comprising: injecting the sample liquid into the analysis device;transferring the sample liquid into an immunoassay cavity that holds a latex reagent sensitized by an antibody that specifically reacts with a particular component in the sample liquid, so as to create an immunoassay solution by an immunoreaction between the sample liquid and the latex reagent;transferring the immunoassay solution into an agglutinative reaction cavity that holds an agglutination reagent, so as to create an agglutinated solution by agglutination reaction between the immunoassay solution and the agglutination reagent; andmeasuring the agglutinated solution by irradiating a light to the agglutinated solution;wherein an average particle size of the latex reagent is in a range from 0.12 μm to 0.31 μm, and a mixing ratio of the antibody-sensitized latex reagent and an antigen inside the agglutination reagent is antigen-excessive. 2. The analysis method according to claim 1, wherein a mean value of particle sizes of agglutinated substances within three minutes of the agglutination reaction between the immunoassay solution and the agglutination reagent is equal to or less than 700 nm. 3. The analysis method according to claim 2, wherein a centrifugal force applied to the agglutinated substances during a measurement is equal to or less than 200 G. 4. The analysis method according to claim 1, wherein the immunoreaction involves having a latex reagent react to a mixed solution that combines the sample liquid with a diluent measured inside the analysis device. 5. The analysis method according to claim 4, wherein the sample liquid is blood, the analysis method further comprising: condensing a blood cell component in the blood by centrifugal force after injecting the blood into the analysis device;collecting a constant amount of blood containing the blood cell component; andmixing the constant amount of blood and the diluent so as to create the mixed solution. 6. The analysis method using the analysis device according to claim 4, further comprising: measuring the mixed solution before the immunoreaction between the mixed solution and the latex reagent. 7. The analysis method according to claim 1, wherein the sample liquid is denaturized by a denaturing regent so as to ensure that an immunoreaction occurs between a specific component in the sample liquid and the latex reagent.