Abstract: A test device and a kit for conducting an assay for the determination of an analyte in a sample comprises (i) a housing (1,2), and within said housing, (ii) a flow matrix (6) allowing liquid to be transported by capillary action and having at least one zone with immobilized capturing agent capable of directly or indirectly binding to the analyte, (iii) a liquid container (13) for sample liquid, and (iv) at least one liquid container for liquid other than sample liquid. The device further comprises (v) separation means (5) between the flow matrix (6) and the liquid containers (13), wherein said separation means (5) are mounted in movable relationship with the liquid containers to in a first position prevent liquid contact of the flow matrix (6) with the liquid containers (13), and in a second position permit liquid receiving contact of the flow matrix (6) with the liquid containers (13).

Abstract: The present invention relates to a solid phase assay device comprising a multi-spot detection zone, and to use thereof in immunochromatographic assays. More precisely, the invention relates to a device for determining analytes in an aqueous sample comprising: an elongate flow matrix (6) allowing lateral transport of fluid therethrough, wherein said matrix comprises a sample application zone (3) and downstream thereof, a detection zone (8) having immobilised capture agents capable of directly or indirectly binding to said analytes, wherein said analytes are detected by allowing a labelled second binding agent to bind directly or indirectly to the analytes. The device is characterised in that the immobilised capture agents are distributed in the detection zone (8) as a plurality of small spots, thereby permitting multi-analyte and/or multi-specificity detection.

Abstract: A device for handling porous solid matrixes (16) in analytic determinations of the type comprising at least one reaction step, which is performed in the very matrixes by absorption of a liquid phase therein, comprises a holder (1) and at least one matrix carrier (2), each of which can retain a matrix (16) while at the same time permitting liquid which surrounds the matrix carrier to substantially unobstructedly be absorbed by the matrix. The holder (1) is provided with at least one gripping body (11) projecting therefrom, each of which can detachably carry a corresponding matrix carrier (2), and at least one squeezing body (11), each of which can be pressed against the porous matrix for squeezing out liquid from the same.

Abstract: An improved process of performing analysis methods based upon biospecific affinity reactions in heterogeneous systems, wherein a ligand dissolved in a liquid is reacted with a receptor immobilized on a carrier, characterized by utilizing as the carrier a porous matrix in the form of a material body having an open capillary pore system capable of absorbing and retaining liquid phase and having such limited void dimensions that the total reaction rate of the biospecific reaction or reactions within the pore system between ligand and immobilized receptor will be at least substantially independent of the diffusion of the ligand in the liquid phase. A porous matrix for use in said process has the characteristics mentioned above.

Abstract: The invention relates to an apparatus for carrying out analyses comprising at least one incubation step and at least one separation step for separating a liquid phase from a phase, which is insoluble in said liquid phase. The apparatus comprises a plurality of reaction vessels (2), making it possible to simultaneously carry out similar working sequences with reaction mixtures in the separate reaction vessels, each of which has a porous bottom (3) connected to a separate chamber (8), the reaction vessels being able to retain the reaction mixture during the incubation steps. According to the invention, there is provided a pressure regulating system, which creates a higher relative pressure in the chambers (8) than in the reaction vessels (2). This pressure difference prevents leakage from the reaction vessels to the chambers.