Abstract: For the detection of compounds containing carbohydrate the compound to be detected is reacted with a conjugate which contains a group which enables a specific binding to the substance to be detected and contains a hapten with a molecular weight from 300 to 1200, afterwards the complex formed is brought into contact with labelled antibodies directed against the hapten and the label is determined in a known way.

Abstract: The present invention provides a process for the production of proteins or protein-containing gene products by transformation of eukaryotic host cells with a recombinant DNA molecule containing the gene for the desired protein, culturing the cells and isolating the gene product after expression, wherein, as host cells, there is used a yeast strain which is deficient in proteases A and B.

Abstract: The present invention provides an immune reactive porous carrier material comprising a porous carrier material with immune complexes precipitated thereon, wherein the porous carrier material is treated with at least one wet-strength agent.The present invention also provides processes for the production of this immune reactive porous carrier material.

Abstract: The invention concerns a DNA which contains(1) at least one of the two regions of the nucleotide sequence SEQ ID NO:1 coding for a protein with a Sau3AI methylase activity or for a protein with a Sau3AI endonuclease activity.(2) a sequence corresponding to the DNA from (1) within the scope of the degeneration of the genetic code or(3) a sequence which hybridizes under stringent hybridization conditions with a DNA from (1) or (2).In addition a vector is disclosed which contains a DNA according to the present invention, in particular under the control of a regulatable closed promoter, as well as microorganisms which are transformed with one or several vectors according to the present invention and the isolation of recombinant Sau3AI endonuclease from the transformed microorganisms.

Abstract: An oligonucleotide probe specific for Neisseria gonorrhoeae is selected from the oligonucleotides RS2* and RS3*, RS2** and RS3**. It can have further nucleotides at its 5' end and/or 3' end. This probe is suitable for the specific detection of nucleic acids of the pathogenic species N. gonorrhoeae by hybrid formation under hybridization conditions.

Abstract: Test carrier for the analysis of fluids with a test field (7) held in a frame (2), in which the frame (2) comprises a top part (3) and a base part (4) and at least the top part (3) comprises a test field opening (6) through which a sample fluid can be applied to the surface (7a) of the test field. Simplified handling and improved analytical reliability are achieved by the fact that the base part (4) comprises a seat (16) for the test field (7) which is surrounded by positioning elements (15) which are higher than the test field (7). The test field opening (6) is greater than the test field (7), so that the rim (18) of the test field is visible. The top part (3) comprises pressure tongues resting on the surface (7a) of the test field (7) and projecting into the test field opening (7).

Abstract: The present invention provides sulphonamides of the general formula: ##STR1## wherein R is a hydrogen or halogen atom, a cyano group or a C.sub.1 -C.sub.6 -alkyl or trifluoromethyl radical, n is 1, 2 or 3, m is 0 or 1 to 5, X is a valency bond, an oxygen atom, a carbonyl group or a --CHOH-- group, A is a valency bond or a carbonyl group and B is a valency bond or an --NH-- group; the physiologically acceptable salts thereof with inorganic and organic acids, as well as the optical isomers thereof.The present invention also provides processes for the preparation of these compounds and pharmaceutical compositions containing them.

Abstract: A reagent supply system for a medical anlytical instrument includes a reagent space provided on the instrument and reagent vessels which are received in the reagent space. In the reagent space there is provided at least one reagent vessel compartment with a bottom, lateral guide elements, and a top guiding element, as well as a front stop. The instrument contains a fluid communication system for connection with a reagent vessel situated in the reagent vessel compartment. On the end face of the reagent vessel compartment is disposed a hollow needle near the bottom surface thereof and extending in a direction which is parallel to the bottom surface. The reagent vessel has on its front wall facing the end face a pierceable seal with a pierceable elastic stopper.

Abstract: The present invention provides cobalamin acid hydrazides of the general formula:B--CO--NH--NH--R--CO--NH--NH).sub.x H (I)wherein B is a residue formed from a cobalamin by the splitting off of a --CONH.sub.2 group, R is a spacer and x is 0 or 1, as well as a process for the preparation thereof.The present invention also provides cobalamin conjugates of the general formula:B--d--CO--NH--NH--R--CO--NH).sub.x N.dbd.GP (II)in which B, R and x have the above-given meanings and d signifies the position of --CO--NH--, as well as a process for the preparation thereof. These cobalamin conjugates are very suitable for use in immunoassays, especially for the determination of cyanocobalamin.

Abstract: An assembly (10) for positioning a prosthetic acetabular cup assembly (110) in a patient's hip is provided. The assembly (10) includes a bearing component (114) having an inner bearing surface (134) for receiving a femoral ball and an outer surface (132) attachable to a shell component (112) The shell component (112) is attached to an acetabulum to replace a natural hip socket. The shell component (112) includes an inner surface (120) defining a cavity (126) for receiving the outer surface (132) of the bearing component (114) therein. The assembly (10) includes a handle (12) attached to a split head (30). The split head (30) is divided into first and second gripping elements (36, 38) that jointly form a gripping surface to engage the inner bearing surface (134) of the bearing component (114). The assembly (10) holds the bearing component (114) at a selected orientation with relation to the shell component (112), and is used to drive the bearing component/shell component (114/112) into the acetabulum.

Abstract: The present invention provides a test carrier for the determination of an analyte from whole blood with the help of reagents contained in the test carrier, said test carrier having a blood application side to which blood is applied, an evaluation side on which, as a result of the reaction of the reagents with the analyte, an optically detectable change takes place, and an erythrocyte separation means between the blood application side and the evaluation side, wherein the erythrocyte separation means includes an integral composite having a first zone, which contains a polymeric film former, kieselguhr and a pigment, and thereupon, with formation of a transition region, a second zone containing a polymeric film-former, formed by liquid coating the first zone facing the blood application side and the second zone facing the evaluation side of the integral composite. The present invention also provides a process for the production of this test carrier and a method for analyzing blood samples using it.

Abstract: The present invention provides a stabilized, NAD(P)H-dependent, soluble nitrate reductase of the assimilatory type, characterized by a molecular weight of about 90,000 D in the case of electrophoresis in the presence of sodium dodecyl sulphate and a residual activity after 3 weeks at 35.degree. C. of more than 60%, obtainable by preparing a suspension of the comminuted starting material in tris/tartaric acid buffer (pH 7-8.5), adding soluble polyethyleneimine thereto in such an amount that 10 to 20% of the nitrate reductase activity passes into the precipitation obtained, separating off the precipitate and working up the supernatant according to conventional biochemical methods of fractionation in the above-mentioned digestion buffer, dialyzing the enzyme solution obtained and lyophilizing in a zwitterionic buffer.

Abstract: A process for the removal of non-specific turbidities in the carrying out of determinations according to the immuno-assay principle, wherein an inorganic boron compound is added to the sample solution in combination with a buffer system.

Abstract: The present invention provides a test carrier for the analysis of a sample liquid with a test layer which contains a ligand fixed to to carrier particles, which ligand reacts with a component of the sample liquid, the test layer having a three-dimensional open structure which is so porous that the sample liquid with the component can penetrate into it, the carrier particles being arranged in the layer in such a manner that the ligand, upon pentration of the sample liquid, comes into contact with the component of the sample, wherein the carrier particles consist of an inorganic material, on the surface of which reactive organic groups are covalently bound as coupling groups, and the ligand is covalently bound to the coupling groups. The present invention also provides processes for the production of such a test carrier and a method for using it.

Abstract: A Neisseria-specific DNA probe is chosen from the group of the oligonucleotides Opa 1, Opa 2, Opa 3, P III, Pil 1, IgA 1 and IgA 2 or from sequences complementary to these and it can have up to 5 further nucleotides at the 5' and/or 3' end. The probe is suitable for the detection of at least one of the pathogenic Neisseria species N. gonorrhoeae and N. meningitidis under hybridization conditions by the detection of the hybrid formation.

Abstract: An apparatus is provided for making color comparisons between a test sample and a plurality of color samples. The color samples are arranged on a circle on a rotatable member and are successively moved into position adjacent a test sample. When an operator determines that a color sample adjacent the test sample is closest in color to the test sample he operates a switch which causes a stored numerical value associated with that sample to be read out and displayed on a display device.

Abstract: Test carrier for analysis of a sample liquid with the help of a specific binding reaction of two bioaffine binding partners, one of which is contained in the sample and one in the reagent system of the test carrier, with several capillary-active test zones (11-16; 21-25) arranged substantially next to one another on a base layer (2). The test zones are in liquid contact with one another so that they form a liquid transport path (20, 30) along which a liquid flows, driven by capillary forces, from a start zone (11, 21), a reaction thereby taking place between the first binding partner and the reagent system containing the second reaction partner, which reaction leads to a labelled species characteristic for the desired analysis.

Abstract: An apparatus is provided for making color comparisons between a test sample and a plurality of color samples. The color samples are arranged on a circle on a rotatable member and are successively moved into position adjacent a test sample. When an operator determines that a color sample adjacent the test sample is closest in color to the test sample he operates a switch which causes a stored numerical value associated with that sample to be read out and displayed on a display device.

Abstract: The present invention is concerned with the use of compounds of the general formula: ##STR1## and of the pharmacologically acceptable salts thereof, as well as of the optical isomers thereof for the preparation of pharmaceutical compositions with antiviral action.The present invention also provides new phospholipid derivatives.

Abstract: The novel type II restriction endonuclease SwaI has the following recognition sequence: ##STR1## and preferably cleaves at the cleavage site indicated by the line. It is preferably obtainable from microorganisms of the genus Staphylococcus.