Abstract: A device for laser projection comprises a first laser diode configured to emit a first linearly polarized laser beam extending along a first polarization axis and a second laser diode configured to emit a second linearly polarized laser beam extending along a second polarization axis that is perpendicular to the first polarization axis. A polarization combiner is configured to combine the first and second linearly polarizing laser beams into a combined laser beam, wherein the combined laser beam comprises one of: (1) circular polarization; and (2) elliptical polarization. A measuring device is configured to measure an intensity of the combined laser beam. A control unit is configured to receive the measured intensity of the combined laser beam and is further configured to adjust an intensity of at least one of: (1) the first laser diode; and (2) the second laser diode.

Abstract: A system for determining the number of passengers in a vehicle, comprising a plurality of sensors arranged to collect data concerning a cabin of the vehicle, wherein the plurality of sensors comprises at least one mm-wave-radar-sensor, and a computation unit, wherein the computation unit is connected to the plurality of sensors and configured to evaluate the data collected by the plurality of sensors in order to determine the number of passengers within the vehicle. Also provided is the vehicle with the system and a method for determining the number of passengers in the vehicle.

Abstract: An optical system (10) for use in an underwater environment is proposed, wherein the optical system (10) comprises a housing which delimits an interior (60) of the optical system (10) with respect to the surroundings (50) in water-tight fashion, and a lens (20) with an outer surface (24), wherein the housing comprises a mount (40), wherein the lens (20) is received in the mount (40) in such a way that the outer surface (24) of the lens (20) is in fluid contact with water of the underwater environment when the optical system (10) is situated in the underwater environment, wherein the outer surface (24) of the lens (20) has an arched form, in particular a convex form, preferably a spherical convex form, wherein the lens (20) has a first arched contact face (28), in particular a spherical contact face, and the mount (40) has a second contact face (48), wherein the lens (20) is arranged in the mount (40) in such a way that the first contact face (28) presses against the second contact face (48) when the pressure

Abstract: The invention relates to a device for the contamination-free delivery and discharge of liquid into and from a reaction vessel 15, having a tube 1, one end of which [lacuna] designed as a first connection fitting 2 for connection to a pipette or the like and the other end of which has a first opening 3. In order to avoid contamination when the reaction vessel is filled with and drained of liquids, it is proposed that a second connection fitting 4, which is in communication with at least a second opening 8, is provided in the vicinity of the first end.

Abstract: Magnetic particles for separating biological mixtures consist of nacreous luster pigments with magnetic properties coated with a biological polymer.

Abstract: The invention concerns the use of an asymmetric porous membrane for the evenly distributed concentration of a substance which is not or not substantially adsorbed to the membrane and which is brought into contact with the membrane in the form of a membrane-wetting solution on the fine-pored side of the membrane.

Abstract: Apparatus to isolate and/or analyze charged biomolecules, preferably nucleic acids, comprising: a vessel made substantially of a rigid plastic comprising a receiving chamber to receive reagents, this receiving chamber being externally accessible through an access aperture of the vessel, further two electrodes which can be moved into the receiving chamber to be in contact with the reagents, further comprising, according to the invention: a tube unit made of electrically non-conducting plastic and of such dimensions and/or being designed and/or affixable in such a way that at least part of its inside surface can be made to contact reagents and/or samples contained in the receiving chamber, the tube unit and one of the electrodes being so configured that this electrode can be brought into contact in the tube unit with reagents and/or samples. The apparatus of the invention is especially suitable to carry out methods to isolate and/or analyze charged biomolecules.

Abstract: An EGR system for an internal combustion engine has a separate, secondary high-temperature cooling loop, in addition to a primary cooling loop. In the secondary cooling loop, coolant flows through a secondary high-temperature exhaust gas cooler, which is located upstream of the primary exhaust gas cooler. A large amount of heat is transferred from the exhaust gases to the coolant in the secondary high-temperature cooling loop. The heat absorbed by the high-temperature coolant is rejected in a secondary high-temperature radiator. Heat absorbed by the primary coolant is rejected in a primary radiator. The two radiators occupy the same amount of frontal area as a single radiator used in a conventional single-stage EGR cooling system, but overall reject more heat to the ambient. In an alternate arrangement, the EGR system for a liquid-cooled internal combustion engine has a single exhaust gas cooler which is cooled by an EGR cooling loop that is independent of the engine cooling system.

Abstract: The invention relates to an apparatus for isolating nucleic acids from biological fluids and suspensions containing nucleic acids, a reaction compartment 17 for receiving an adsorption medium 100 being connected to a removal compartment 50, and the nucleic acids being able to be moved and enriched from the reaction compartment 17 into the removal compartment 50 by an electrophoresis apparatus 20a, 20b.

Abstract: Device for the isolation of nucleic acids from a liquid sample by introducing the liquid into the device through an inlet opening and passage of the sample through a nucleic acid binding material and discharging of the resulting liquid through an outlet opening, wherein the nucleic acid binding material is inserted through the outlet opening during the manufacture of the device and the outlet opening is narrowed in order to hold the material. The device is particularly simple and reliable to manufacture but yet ensures that nucleic acids can be isolated without contamination.

Abstract: Described is an apparatus for the contamination-free isolation of nucleic acids from biological fluids and suspensions containing nucleic acids comprising: a reaction compartment for holding an adsorption medium laden with nucleic acids; connected via a channel to a removal compartment; wherein the nucleic acids can be moved by an electrophoresis device from the reaction compartment into the removal compartment and enriched there; and the reaction compartment can be charged via a charging orifice and drained via a draining orifice being located essentially opposite of the charging orifice.

Abstract: Device for the isolation of nucleic acids from a liquid sample by introducing the liquid into the device through an inlet opening and passage of the sample through a nucleic acid binding material and discharging of the resulting liquid through an outlet opening, wherein the nucleic acid binding material is inserted through the outlet opening during the manufacture of the device and the outlet opening is narrowed in order to hold the material. The device is particularly simple and reliable to manufacture but yet ensures that nucleic acids can be isolated without contamination.

Abstract: A method for the repeated transfer of liquids from one of several storage containers into a transfer container wherein protective tips are placed onto a tip of a pipette in order to avoid contamination.

Abstract: System for the automatic operation of reactions using several vessels which can be closed by individual closures using a device for automatically opening the closures.

Abstract: A method for the repeated transfer of liquids from one of several storage containers into a transfer container wherein protective tips are placed onto a tip of a pipette in order to avoid contamination.

Abstract: Device for the treatment of nucleic acids from the sample, comprising a first reaction chamber for separating the nucleic acids from other sample components, and a second reaction chamber for the amplification of the nucleic acids, connected to said first reaction chamber via a controllable transport path.

Abstract: Blood lancet device (1) for withdrawing blood from a patient for diagnostic purposes comprises a housing (10), a lancet holder (11) movable within the housing (10) for retaining a non-rotatable lancet (4) having a plastic lancet body (31), a lancet needle (33) fixed in the lancet body (31), a lancet drive (12) to move the lancet holder in a puncturing and retraction direction, an exchangeable skin-contact part (5) having an outlet opening (6) for the lancet (4) and a contact surface (42) for pressing against a patient's skin.

Abstract: Blood lancet device for withdrawing blood for diagnostic purposes, in which with the aid of a lancet drive (3) in a housing (1) a lancet holder (6) with a lancet (34) positioned in it and moveable along a predetermined, straight puncture path is moved until the tip (35) of the lancet emerges from the outlet (84), in order to produce a wound in a body part adjoining the outlet (84). The lancet holder (6) also serves to retract the lancet (34) into a position in which the tip (35) is again positioned within the housing (1).In order to make possible a puncture involving especially little pain, the lancet drive (3) has a rotary/sliding transmission system (4) whose input side (16) is formed by a transmission member which is rotatable about an axis of rotation parallel to the predetermined puncture path.

Abstract: The invention concerns a method for the detection of an analyte in a sample liquid by an enzyme-immunoassay in which an enzyme-labelled compound is partitioned between a solid and a liquid phase and the amount of enzyme label in the liquid phase outside the solid phase is determined as a measure of the concentration of the analyte. The measurement is carried out in a non-porous molding having the liquid phase contained therein in contact with the solid phase. The method is particularly suitable for carrying out in a cuvette which can be filled via the porous matrix or on a test strip having a space in contact with the solid phase.

Abstract: Blood lancet device for withdrawing blood for diagnostic purposes, in which with the aid of a lancet drive (3) in a housing (1) a lancet holder (6) with a lancet (34) positioned in it and moveable along a predetermined, straight puncture path is moved until the tip (35) of the lancet emerges from the outlet (84), in order to produce a wound in a body part adjoining the outlet (84). The lancet holder (6) also serves to retract the lancet (34) into a position in which the tip (35) is again positioned within the housing (1).In order to make possible a puncture involving especially little pain, the lancet drive (3) has a rotary/sliding transmission system (4) whose input side (16) is formed by a transmission member which is rotatable about an axis of rotation parallel to the predetermined puncture path.