Abstract: A system for collecting and separating biological material includes a centrifuge tube, a separation tube having an open bottom, a cap, a plug for temporarily sealing the open bottom of the separation tube, and a separation medium disposable within the centrifuge tube. The centrifuge tube and the separation tube sealingly and releasably couple to the cap, such that, when coupled, the separation tube is positioned within the centrifuge tube. The cap is configured to facilitate and/or regulate the introduction of air, gas, or other matter into the separation tube. When fully sealed, the separation tube may be placed under a vacuum condition, whereby a needle apparatus is used to facilitate introduction of matter into the separation tube. When the separation tube is positioned within the centrifuge tube, the bottom portion of the separation tube is submersed in the separation medium.

Abstract: A system for collecting and separating biological material includes a centrifuge tube, a separation tube having an open bottom, a cap, a plug for temporarily sealing the open bottom of the separation tube, and a separation medium disposable within the centrifuge tube. The centrifuge tube and the separation tube sealingly and releasably couple to the cap, such that, when coupled, the separation tube is positioned within the centrifuge tube. The cap is configured to facilitate and/or regulate the introduction of air, gas, or other matter into the separation tube. When fully sealed, the separation tube may be placed under a vacuum condition, whereby a needle apparatus is used to facilitate introduction of matter into the separation tube. When the separation tube is positioned within the centrifuge tube, the bottom portion of the separation tube is submersed in the separation medium.

Abstract: A system for collecting and separating biological material includes a centrifuge tube, a separation tube having an open bottom, a cap, a plug for temporarily sealing the open bottom of the separation tube, and a separation medium disposable within the centrifuge tube. The centrifuge tube and the separation tube sealingly and releasably couple to the cap, such that, when coupled, the separation tube is positioned within the centrifuge tube. The cap is configured to facilitate and/or regulate the introduction of air, gas, or other matter into the separation tube. When fully sealed, the separation tube may be placed under a vacuum condition, whereby a needle apparatus is used to facilitate introduction of matter into the separation tube. When the separation tube is positioned within the centrifuge tube, the bottom portion of the separation tube is submersed in the separation medium.

Abstract: A system for separating biological material includes a centrifuge tube, a separation tube having an open bottom, a cap, and a separation medium disposable within the centrifuge tube and the separation tube. The centrifuge tube and the separation tube sealingly and releasably couples to the cap, such that, when coupled, the separation tube is positioned within the centrifuge tube. The cap is configured to facilitate and/or regulate air- or gas-flow between an area outside of the cap and an interior of the separation tube. When the separation tube is positioned within the centrifuge tube, the open bottom of the separation tube is submersed in the separation medium. The system also includes a hollow needle coupled to a means for regulating a flow of air, gas, or other matter. The needle is insertable through the cap or plug, and is used to facilitate the introduction of matter into the separation tube.

Abstract: A system for collecting and separating biological material includes a centrifuge tube, a separation tube having an open bottom, a cap, a plug for temporarily sealing the open bottom of the separation tube, and a separation medium disposable within the centrifuge tube. The centrifuge tube and the separation tube sealingly and releasably couple to the cap, such that, when coupled, the separation tube is positioned within the centrifuge tube. The cap is configured to facilitate and/or regulate the introduction of air, gas, or other matter into the separation tube. When fully sealed, the separation tube may be placed under a vacuum condition, whereby a needle apparatus is used to facilitate introduction of matter into the separation tube. When the separation tube is positioned within the centrifuge tube, the bottom portion of the separation tube is submersed in the separation medium.

Abstract: A system for separating biological material includes a centrifuge tube, a separation tube having an open bottom, a cap, and a separation medium disposable within the centrifuge tube and the separation tube. The centrifuge tube and the separation tube sealingly and releasably couples to the cap, such that, when coupled, the separation tube is positioned within the centrifuge tube. The cap is configured to facilitate and/or regulate air- or gas-flow between an area outside of the cap and an interior of the separation tube. When the separation tube is positioned within the centrifuge tube, the open bottom of the separation tube is submersed in the separation medium. The system also includes a hollow needle coupled to a means for regulating a flow of air, gas, or other matter. The needle is insertable through the cap or plug, and is used to facilitate the introduction of matter into the separation tube.

Abstract: A multifunctional system for particle separation and/or treatment for the usage in biological and medical research, to detect and to treat diseases with a modular system consisting out of the filter/strainer device and the auxiliary devices lower connector with tube adaptor and upper screw cap connector. All parts of the modular system can be airtight connected and by means of a valve used with higher pressure, lower pressure or without pressure equalization.

Abstract: A method and a device for defect-size evaluation of defects in a test object in ultrasonic testing is provided. In particular, the method and device also allows systematic determination of defect sizes based on the SAFT method. This is done by simulating defects in a test object on the basis of a defined test scenario, and comparing these simulations with actually recorded measured values.

Abstract: A device and a method for detecting at least one defect in a test object (2). At least one test head (1) radiates an ultrasonic signal at different measuring points (MP) into the test object (2) with each point at an insonation or radiation angle (?) in order to ascertain multiple measurement data sets (MDS). The angle is constant for each data set (MDS). An analyzing unit (4) carries out an SAFT (Synthetic Aperture Focusing Technique) analysis for each ascertained measurement data set (MDS) using a common reconstruction grid (RG) inside the test object (2) in order to calculate an SAFT analysis result for each measurement data set (MDS). The analyzing unit (4) superimposes the calculated SAFT analysis results in order to calculate an orientation-independent defect display value (SRP) for each reconstruction point (RP) of the common reconstruction grid (RG).

Abstract: A cell strainer is described consisting of an integrated vibrating mechanism to prevent clogging up the mesh by larger components.

Abstract: A cell strainer based particle separation system is described consisting of a functionalized mesh and micro-particle smaller than the mesh size. The micro-particles carry at least two binding moieties, one binding on the mesh-fibers, and the second specific to the selected cells. The selected cells can be separated from the biological liquid, modified, detached, analyzed, cultivated or otherwise manipulated.

Abstract: A method and a device for defect-size evaluation of defects in a test object in ultrasonic testing is provided. In particular, the method and device also allows systematic determination of defect sizes based on the SAFT method. This is done by simulating defects in a test object on the basis of a defined test scenario, and comparing these simulations with actually recorded measured values.

Abstract: A technique is provided for determining an orientation of a defect present within a mechanical component using at least one ultrasonic head that applies ultrasonic signals to the mechanical component starting from various measurement points. Echo ultrasonic signals reflected by a point to be analyzed present within the component back to the measurement points are received by the same or a different ultrasonic head. A data processing unit analyzes the received echo ultrasonic signals as a function of a sound emission direction between each measurement ping and the point to be analyzed for determining the orientation of the defect. A distance between the measurement point and the point to be analyzed is calculated for every measurement point as a function of a signal propagation time between the point in time of emitting the ultrasonic signal and the point in time of receiving the echo ultrasonic signal reflected by a defect.

Abstract: A sample disc for ultrasonic disc testing equipment includes a cut-out defining a lateral face extending along a radius of the sample disc and along an axis of symmetry of the sample disc. At least one planar sample defect is created through this lateral face of the disc.

Abstract: A multifunctional system for particle separation and/or treatment for the usage in biological and medical research, to detect and to treat diseases with a modular system consisting out of the filter/strainer device and the auxiliary devices lower connector with tube adaptor and upper screw cap connector. All parts of the modular system can be airtight connected and by means of a valve used with higher pressure, lower pressure or without pressure equalization.

Abstract: A technique is provided for determining an orientation of a defect present within a mechanical component using at least one ultrasonic head that applies ultrasonic signals to the mechanical component starting from various measurement points. Echo ultrasonic signals reflected by a point to be analyzed present within the component back to the measurement points are received by the same or a different ultrasonic head. A data processing unit analyzes the received echo ultrasonic signals as a function of a sound emission direction between each measurement ping and the point to be analyzed for determining the orientation of the defect. A distance between the measurement point and the point to be analyzed is calculated for every measurement point as a function of a signal propagation time between the point in time of emitting the ultrasonic signal and the point in time of receiving the echo ultrasonic signal reflected by a defect.

Abstract: The invention describes an appliance and a method, with the help of which specific bio-particles, but also dissolved bio-molecules can be recognized in and separated from fluids making use of suitable carriers and known immobilization methods. The appliance can be used both discontinuously and also for direct and continuous treatment of fluids. Fields of application of the invention are animals, bio-technology (including biological research) and medicinal diagnostics. Areas of application of the invention comprise, among others, therapy of humans, in particular direct treatment of blood.

Abstract: A device and a method for detecting at least one defect in a test object (2). At least one test head (1) radiates an ultrasonic signal at different measuring points (MP) into the test object (2) with each point at an insonation or radiation angle (?) in order to ascertain multiple measurement data sets (MDS). The angle is constant for each data set (MDS). An analyzing unit (4) carries out an SAFT (Synthetic Aperture Focusing Technique) analysis for each ascertained measurement data set (MDS) using a common reconstruction grid (RG) inside the test object (2) in order to calculate an SAFT analysis result for each measurement data set (MDS). The analyzing unit (4) superimposes the calculated SAFT analysis results in order to calculate an orientation-independent defect display value (SRP) for each reconstruction point (RP) of the common reconstruction grid (RG).

Abstract: The invention relates to a regeneratable filtering and adsorbing system, combining the properties of membrane filtration with those of particle-based adsorption in a closed housing.

Abstract: A method for the non-destructive material testing of a test object at least solid in some regions by subjecting the test object to ultrasonic waves and capturing the ultrasonic waves reflected within the test object. The method includes the steps, computer-supported dividing of the test object into a prescribed number of volume elements, subjecting the test object to ultrasound on a plurality of surface elements while probing the surface or at least one surface segment of the test object, capturing the sound waves reflected at the volume element while probing the plurality of surface elements on the surface or at least the surface segment of the test object, and in-phase addition of the sound waves reflected at the same volume elements and captured at various surface elements of the surface of the test object. Angle-dependent amplitude distribution is used in the sound field of the test head.