Abstract: The present invention provides a microfluidic device capable of reacting an enzyme or other agent with a substantially purified polypeptide. In one embodiment of the present invention, the microfluic device comprises a plurality of reaction channels wherein the substantially purified polypeptide is delivered to a reaction channel. Once confined within the reaction channel, the substantially purified polypeptide engages the enzyme or agent and produces a reaction product. In a preferred embodiment of the present invention, the reaction product is concentrated at a charged membrane prior to being removed from the microfluidic device. Additionally, the present invention provides a method of concentrating a positive analyte at a positively charged membrane and a negative analyte at a negatively charged membrane. Once concentrated, the analytes may be removed from the microfluidic device.

Abstract: A method of delivering oxygen to a biological entity comprising of dissolving oxygen into a perfusate and forcing the perfusate through the biological entity whereby substantially high levels of oxygen are available to satisfy the biological demand of the biological entity. An apparatus for supplying oxygen to a biological entity whereby substantially high levels of oxygen are available to satisfy the metabolic demand of said biological entity. An apparatus for supplying metabolic supplements to a biological entity whereby the effect of said metabolic supplement on said biological entity can be monitored. The method and apparatus keeps a biological entity such as an organ viable at a range of temperatures while in an aerobic state. This allows the study of said organ from a physiological or experimental standpoint. It allows said organ to be transplanted with little or no reperfusion injury, thus increased survivability over the prior art.

Abstract: A chemical reaction circuit for cell-free protein synthesis characterized by, as a chemical reaction circuit for synthesizing a protein, having at least one reagent tank for storing a reagent for the protein synthesis and/or a reagent for detecting a product, a unidirectional valve for preventing the reverse-flow of the reagent(s), and a reaction tank connected to the reagent tank(s) via the unidirectional valve. This circuit is usable as a micro reactor whereby cell-free protein synthesis can be carried out.

Abstract: The invention features modular cell culturing devices including one or more flat-plate modules, and is based on the discovery that if the flows of liquid medium and oxygenated fluid are separated by a gas-permeable, liquid-impermeable membrane, and the cells are grown attached to the liquid side of the membrane, the device can be used to culture cells with transport of oxygen through the membrane (i.e., direct oxygenation), without regard for the flow rate of the liquid medium passing through the device. The new flow-through cell culturing devices can thus be used to culture cells, e.g., hepatocytes, with high levels of cell function in organ, e.g., liver, assist systems, for production of cells, for production of cell-derived products, such as, proteins or viruses, or for systems to treat biological liquids to remove toxins, such as, ammonia, or add cell-synthesized products, or both.

Abstract: A method and apparatus for embedding cells that utilizes a flow-through embedding technique maximizes the efficiency of extractions and decreases time for embedding the cell fragments, minimizes cell loss, and automatically positions cell samples at the position in which a microtome blade will section them. The apparatus includes a cell flow pathway defined by an inflow tube for delivering cell fragments from a cell sample to a sample port. The sample port is in fluid communication with a tissue cassette having attached thereto a filter. The cell flow pathway is in communication with a reagent flow pathway for delivering the reagents through the sample port to the cassette. The apparatus is configured such that the application of pressure directs the cell fragments from the cell sample through the cell flow pathway, and effects delivery of the reagents through the reagent flow pathway.

Abstract: The present invention provides a method for synthesis of polypeptides in a cell-free system. In this method, products of synthesis are separated into a low molecular weight fraction and a high molecular weight fraction, with the high molecular weight fraction containing the target polypeptide. The method calls for the removal of at least a portion of the low molecular weight fraction via a porous barrier.

Abstract: The present invention provides a variety of microscale bioreactors (microfermentors) and microscale bioreactor arrays for use in culturing cells. The microfermentors include a vessel for culturing cells and means for providing oxygen to the interior of the vessel at a concentration sufficient to support cell growth, e.g., growth of bacterial cells. Depending on the embodiment, the microfermentor vessel may have various interior volumes less than approximately 1 ml. The microfermentors may include an aeration membrane and optionally a variety of sensing devices. The invention further provides a chamber to contain the microfermentors and microfermentor arrays and to provide environmental control. Certain of the microfermentors include a second chamber that may be used, e.g., to provide oxygen, nutrients, pH control, etc., to the culture vessel and/or to remove metabolites, etc. Various methods of using the microfermentors, e.g., to select optimum cell strains or bioprocess parameters are provided.

Abstract: The invention provides a cell/tissue culture apparatus for applying a physical stimulation necessary for the proliferation and growth of a cell or tissue to a material to be cultivated serving as a cell or tissue to be cultivated, thereby realizing the culture as desired and protecting the material to be cultivated from contamination of various bacteria and so forth.

Abstract: A filtration assembly (10) for use in collecting a fluid sample possibly containing microorganisms, and capturing the microorganisms of interest in the sample such that the captured microorganisms can be subsequently detected. The filtration assembly includes a sample reservoir (20) for collecting and holding the fluid sample to be filtered, a fluid port (38) and a vent (70) in communication with the sample reservoir, a filter element (45) disposed in a flow path between the sample reservoir and fluid port, and a cover member (50) detachably covering the sample reservoir.

Abstract: A sampling device for detecting airborne particles has two parallel substantially identical intake passages. Each intake passage, in close proximity to the other, and has an inlet, a sampling filter intersecting the passage, means for drawing ambient air through the inlet, and sampling filter. The sampling filter is mounted on a filter magazine that has a plurality of sampling filters. A motor is provided for sequentially moving successive sampling filters on the magazine into the air flow. The sampling device accordingly captures two substantially identical samples from the parallel intake passages.

Abstract: A cell culture bag for culturing cells, cellular aggregates, particles, tissues and organoids is disclosed. The cell culture bag is a flexible and disposable culture bag that fits within a bag support chamber of a bioreactor. The cell culture bag has an inlet means and an outlet means for the introduction and removal of media. Certain embodiments of the culture bag have an inlet and outlet fluid coupling swivel joint and/or perforated perfusion tubes extending from the inlet means into the interior of the bag to assist in mass transfer and mixing the media to maintain an even temperature throughout the culture bag.

Abstract: A bioreaction module for biochemical reactions, in particular for cell-free polypeptide biosynthesis, having a housing (1) including a system chamber (12) and a supply chamber (10), wherein the system chamber (12) contains a producing system during the biochemical reaction and the supply chamber (10) contains a supply liquid during the biochemical reaction, and the system chamber (12) and the supply chamber (10) are separated by a semi-permeable membrane (7). The housing (1) comprises a system chamber element (5) and at least one supply chamber element (3) between which the semi-permeable membrane (7) is mounted in such a manner that the system chamber (12) is defined by the system chamber element (5) and the semi-permeable membrane (7) and the supply chamber (10) is defined by the supply chamber element (3) and the semi-permeable membrane (7).

Abstract: This process is unique in photosynthetic carbon sequestration. An on-site biological sequestration system directly decreases the concentration of carbon-containing compounds in the emissions of fossil generation units. In this process, photosynthetic microbes are attached to a growth surface arranged in a containment chamber that is lit by solar photons. A harvesting system ensures maximum organism growth and rate of CO2 uptake. Soluble carbon and nitrogen concentrations delivered to the cyanobacteria are enhanced, further increasing growth rate and carbon utilization.

Abstract: A compost tea system uses a water-holding tank for containing process water. Compost is immersed into the water in the tank in baskets defining a filter media. Air is pumped into membrane disk diffuser modules in the tank and the liquid is sparged with fine bubbles to thoroughly agitate the liquid, extract nutrients and microorganisms from the compost, and to ensure a high concentration of dissolved oxygen in the liquid. The high level of oxygen selects for desired aerobic organisms to produce a rich compost tea. The finished tea is drained out of the tank and the tank and its components are easily cleaned and sanitized.

Abstract: An improved culture vessel or bioreactor for growing cells, cellular aggregates, tissue particles or tissue “organoids” and methods for using same which includes a housing having at least one chamber defined by a curved wall symmetrical about an axis. The perfused version of the vessel has at least one inlet and at least one outlet and at least one filter in fluid communication with at least one of the inlets or outlets structured to pass culture media but retain cells, cellular aggregates or tissues within the culture chamber. The batch culture version of the vessel has at least part of the vessel wall made of a gas permeable material. The vessel housing is rotated about the horizontal or proximate horizontal axis to suspend the cells, in an unobstructed, three-dimensional or toroidal flow. The chamber has a substantially ellipsoid, oblate ellipsoid, spherical or oblate spherical shape and an unobstructed volume for growth of cells, cellular aggregates or tissues.

Abstract: A microprocessor controlled and instrumented bioreactor for conditioning intravascular tissue engineered medical products. One bioreactor design including an integrated pump to provide a relatively small volume of fluid nutrient. The microprocessor control providing measurement and control of the fluid flow and tissue displacement and subsequent determination of material properties. One design includes a flexible joint providing motion of the treated tissue in the axial, bending and torsional direction.

Abstract: Disclosed is a bioreactor apparatus having a bed of buoyant media pellets floating within a filtrate to be processed. The apparatus includes a tank (22) having a peripheral wall for containing filtrate (34) and a bed (36) of media pellets (38). A central manifold (100) is rotatably supported within the tank, the central manifold being mounted for rotation about a vertical axis (22) and having a plurality of longitudinally spaced openings (140) intermediate its ends, the openings adapted to eject filtrate in a generally horizontal direction and along a substantially vertical plane toward the wall of the tank, cyclically fluidize pellets in a directly narrow zone. In a preferred aspect, there is also a thrust manifold (140), generally parallel to the axis of the central manifold and having a plurality of longitudinally spaced openings intermediate its ends directed horizontally and generally perpendicularly to the plane.

Abstract: A two-chamber perfusion bioreactor counteracts a significant amount of shear stress while allowing high nutrient transfer and removal of waste and/or valuable bio-products, e.g., protein, hormones, growth factors, and monoclonal antibodies without disturbing the cell culture. Cells and tissues, contained in the growth chamber, are suspended in the growth media by rotation of the vessel and are separated by a porous membrane from the feeding chamber. Nutrients and gases are transferred across the membrane from the feeding chamber to the growth chamber. Even dispersion of nutrients along the membrane barrier is accomplished through a novel nutrient dispersion flow path. The flow path is created by flowing media out a center shaft in the vessel and along the front of the nutrient dispersion disk. The fluid then flows around the back of the nutrient dispersion disk and exits the outer center return shaft.

Abstract: A cell culture device for inducing shear stress and on substrate strain on cells. The device includes a cell culture membrane and a flow pathway for moving fluid across cells growing on the membrane to apply shear stress on the cells.

Abstract: An apparatus for high-throughput analysis of compound absorption in a controlled environment that closely resembles in-vivo conditions. The apparatus includes at least one tissue-receiving enclosure that is capable of interfacing (e.g., via transfer of fluids, electronically, etc.) with a variety of preparative devices and analytical instrumentation. In some variations, the tissue-receiving enclosure is formed from two housings, which, when engaged, have a capsular shape. The enclosure receives a tissue sample in the form of an un-everted or everted intestinal segment or tubular artificial membrane. The tissue sample is coupled to a generally cylindrical tissue support. The tissue support and the enclosure are axially aligned, and openings at the ends of the enclosure align with openings at the ends of the tissue support. Two feed fittings, one for each end of the enclosure, forcefully mate with the aligned openings in the housing and the tissue support.

Abstract: The invention relates to new flow-through cell culturing devices that include plates arranged in parallel and spaced to control the flow patterns and velocity of liquid medium flowing between the plates. The devices can also include gas-permeable, liquid impermeable membranes arranged between the plates. The devices can be used to culture cells, such as hepatocytes, at high levels of mass transport of nutrients, oxygen, and waste products, yet low levels of shear stress for extended periods of time and with high levels of cell function, e.g., in organ assist systems. The invention also includes new culturing plates for use in the devices, and methods of manufacturing these plates.

Abstract: The present invention provides improved chlortetracycline-containing animal feed compositions and processes and apparatuses for their preparation. In certain embodiments, raw fermentation broth comprising chlortetracycline is divided into two portions. The first portion is mixed with a compound that complexes chlortetracycline. The second portion is acidified and the solids are removed. The acidified liquid is treated with a complexing agent to produced a chlortetracycline complex. The first and second portions thus treated are then mixed and the mixture is passed on to a filter press or other means for separation of the solids to produce a wet cake comprising complexed chlortetracycline.

Abstract: For direct and on-line study of the physiological states of cell cultures, a robust flow injection system has been designed and interfaced with flow cytometry (FI-FCM). The core of the flow injection system includes a microchamber designed for sample processing. The design of the microchamber allows not only an accurate on-line dilution but also on-line cell fixation, staining, and washing. The flow injection part of the system was tested by monitoring the optical density of a growing E.coli culture on-line using a spectrophotometer. The entire growth curve, from lag phase to stationary phase, was obtained with frequent sampling. The system is thus particularly useful since it operates automatically without direct operator supervision for extended time periods.

Abstract: A bioreactor is described comprising: at least one cartridge having disposed therein at least one collagen substrate comprised of a collagen sponge layer and a nonporous to cells, semipermeable collagen layer; a substrate support that retains the collagen substrate within the cartridge; a first compartment between the collagen sponge layer and the inner surface of the first side of the cartridge casing and a second compartment between the nonporous to cells, semipermeable collagen layer and the inner surface of the second side of the cartridge casing; inlet and outlet means for transferring a first medium and a first cell type to the first compartment and inlet and outlet means for transferring a second medium and a second cell type to the second compartment.

Abstract: A disposable bioreactor for perfusion cell culture. Cells are grown in a plastic bag that is rocked and aerated on a mechanical platform. The bioreactor bag contains a filter that allows liquid to be removed from the bioreactor-without losing cells. Nutrients may be added through another port. The perfusion filter is constructed such that it can move freely on the liquid surface. The filter is flicked rapidly across the surface as a result of the rocking motion of the bioreactor and this tangential motion of the filter keeps it from clogging. A weight-based control system regulates feed and harvest rates and allows weeks of continuous operation. This invention has numerous applications in biotechnology and medicine.

Abstract: A perfusion chamber includes a porous oocyte support structure. A continuously sloped top surface and a receiving well in the support structure entrap the underside of the oocyte, thereby localizing the cell in a predetermined fixed position within the reach of dedicated voltage-clamp microelectrodes. A test solution is delivered continuously at the top of the chamber, above the oocyte, and withdrawn from the bottom of the chamber, below the oocyte. The porosity of the support material enables the continuous perfusion of test solution around the membrane of the oocyte, including its bottom portion that is held firmly in contact with the holding well. The geometry of the holding well is selected such as to ensure the automatic and precise placement of the oocyte by gravity and to optimize the pressure distribution over its membrane, thereby minimizing the probability of rupture or other damage to the cell.

Abstract: The present invention includes a bioreactor support system that provides an improved way to culture large quantities of mammalian cells. Mammalian cells are extremely sensitive to their environment, undergoing a programmed cell death in response to nutrient deprivation, growth factor withdrawal, oxygen starvation and excess shear levels. The present invention includes a bioreactor support system which permits the culture of cells at high density and prevents cell death by providing enhanced oxygen delivery to the cells without excessive shear; maintaining cell secreted or exogenously added low molecular weight products (e.g., growth, differentiation and maintenance factors) in the culture space during perfusion culture; and provides the ability to feed the cultures without dilution of the conditioned media. The improved bioreactor support system features two flow paths emanating from a central integrating chamber.

Abstract: A thermal cycling device for biological samples. The thermal cycling device may include a sample block, an annular plate, and a plurality of spring devices interposed between the sample block and the annular plate. The sample block has a plurality of openings for receiving sample wells of a sample well tray. The annular plate may be positioned adjacent the outer periphery of the sample block and may be configured to abut a bottom surface of the sample well tray when the sample well tray is positioned thereon. The plurality of spring device may be interposed between the sample block and the annular plate to urge the annular plate and sample well tray away from the sample block.

Abstract: A disposable bioreactor for perfusion cell culture. Cells are grown in a plastic bag that is rocked and aerated on a mechanical platform. The bioreactor bag contains a filter that allows liquid to be removed from the bioreactor without losing cells. Nutrients may be added through another port. The perfusion filter is constructed such that it can move freely on the liquid surface. The filter is flicked rapidly across the surface as a result of the rocking motion of the bioreactor and this tangential motion of the filter keeps it from clogging. A weight-based control system regulates feed and harvest rates and allows weeks of continuous operation. This invention has numerous applications in biotechnology and medicine.

Abstract: The present invention provides a method for synthesis polypeptides in a cell-free system by which products of synthesis are branched in a low molecular weight fraction and a fraction which contains high molecular weight components with the target polypeptide, the main part of the low molecular weight fraction is removed via at least one part of the second porous barrier, the ratio of the volume of the fractions of feed solution and expendable components to the volume of the fraction containing the target polypeptide is chosen, modes of supply of the feed solution and expendable components of the fraction are realized.

Abstract: Methods and apparatuses for removing microbial contaminants from a flowing fluid in a cell culture incubator are disclosed. Some embodiments of the invention provide a cell culture incubator including a chamber, an airflow passage through which gasses circulate within the chamber, a filter configured to filter gasses that flow through the airflow passage and chamber, and a blower for circulating gasses through the airflow passage, chamber and filter. The blower includes a structural component at least partially formed from an anti-microbial material.

Abstract: This concerns a device whose filtering membrane (4) is gripped annularly at the periphery between a first member (9) forming part of an intake body (2) and a second member (32) forming part of a drainage body (3) with one out of the first member and second member having an elastomer seal (13) by means of which it comes into contact with the membrane (4), and whose locking means (7, 31) are adapted to allow the opening of the device by requiring only a separation movement between said first member (9) and said second member (32).

Abstract: This concerns a device whose filtering membrane is gripped annularly at the periphery between a first member forming part of an intake body and a second member forming part of a drainage body with one out of the first member and second member having an elastomer seal by means of which it comes into contact with the membrane, and whose locking means are adapted to allow the opening of the device by requiring only a separation movement between said first member and said second member.

Abstract: The invention features modular cell culturing devices including one or more flat-plate modules, and is based on the discovery that if the flows of liquid medium and oxygenated fluid are separated by a gas-permeable, liquid-impermeable membrane, and the cells are grown attached to the liquid side of the membrane, the device can be used to culture cells with transport of oxygen through the membrane (i.e., direct oxygenation), without regard for the flow rate of the liquid medium passing through the device. The new flow-through cell culturing devices can thus be used to culture cells, e.g., hepatocytes, with high levels of cell function in organ, e.g., liver, assist systems, for production of cells, for production of cell-derived products, such as, proteins or viruses, or for systems to treat biological liquids to remove toxins, such as, ammonia, or add cell-synthesized products, or both.

Abstract: The present invention provides a feedback controlled bioculture platform for use as a precision cell biology research tool and for clinical cell growth and maintenance applications. The system provides individual closed-loop flowpath cartridges, with integrated, aseptic sampling and routing to collection vials or analysis systems. The system can operate in a standard laboratory or other incubator for provision of requisite gas and thermal environment. System cartridges are modular and can be operated independently or under a unified system controlling architecture, and provide for scale-up production of cell and cell products for research and clinical applications. Multiple replicates of the flowpath cartridges allow for individual, yet replicate cell culture growth and multiples of the experiment models that can be varied according to the experiment design, or modulated to desired cell development of cell culture end-points.

Abstract: A microbial membrane reactor for use in flow systems comprises a first element to receive the microorganisms and a second element to receive the flow channels. The two elements have planar interior surfaces which are pressed together separated by a membrane impervious to the microorganisms. The flow channels arranged in or on the surface of the second element serve to transport the liquid along the membrane so that the liquid can interact with the microorganisms arranged on the other side of the membrane. The geometry of the flow pathway and thus the geometry of the flow channels can be easily altered, in respect of the length, width and height of the channel, and adapted to practical requirements.

Abstract: The invention provides a method for detection of receptor- or ion channel-modulators (e.g., antagonists, blockers, etc.). The method comprises fractionating a sample by using a liquid-based separation means (e.g., such as a capillary electrophoresis device), and feeding the fractions containing the modulators directly to a biosensor. The biosensor is activatable by a receptor agonist and produces a measurable response as a result of this activation. Preferably, the agonist is fed to the biosensor through the liquid-based separation means, together with fractions containing the modulators (e.g., antagonists or blockers). The presence of a modulator is detected by monitoring a change in the response of the biosensor, e.g., by measuring changes in electrical properties of the biosensor (such as through patch clamp analysis).

Abstract: An in vitro system for perfusion of cultured cells comprising one or more cell culture devices, one or more reservoirs, and a perfusion mechanism for providing a fluid flow between the one or more cell culture devices and the one or more reservoirs. Also provided is a method of using the in vitro system to contact cultured cells, contained in the one or more cell culture devices, with a biological substance. The biological substance may be mixed with medium, and then the medium may be circulated through the one or more cell culture devices so that the biological substance contacts cultured cells contained in the one or more cell culture devices.

Abstract: A disposable bioreactor for culturing microorganisms and cells is provided. The bioreactor is suitable for use by individuals not skilled in microbiology or aseptic technique. It is constructed of flexible or semi-flexible waterproof sheets to form a container designed to provided mixing and gas exchange to microorganisms cultured therein. Mixing and gas exchanged are achieved by bubbling gas through the culture, either from a single locus at the lowermost apex of a container having a wedge-shaped or rounded bottom, or from multiple loci across a flat-bottomed container. Also provided is a kit for culturing a selected microorganism, preferably an entomopathogenic nematode or other organism useful as a biopesticide.

Abstract: The invention provides a device and process for recellularizing essentially acellular or devitalized tissue grafts, including for example essentially acellular or devitalized vascular tissue grafts, derived from human or animal sources, or as constructed using any number of tissue engineering methodologies. The process includes repopulating and reendothelializing an essentially acellular or devitalized tissue graft. The device is useful for producing a repopulated tissue graft from an essentially acellular or devitalized tissue, as well as for producing an essentially acellular or devitalized tissue graft.

Abstract: A device for use with an ultrasonic transducer to lyse components of a fluid sample comprises a cartridge having a lysing chamber, an inlet port in fluid communication with the lysing chamber, and an outlet port for exit of the sample from the lysing chamber. The inlet and outlet ports are positioned to permit flow of the sample through the lysing chamber, and the chamber contains at least one solid phase for capturing the sample components to be lysed as the sample flows through the chamber. The lysing chamber is defined by at least one wall having an external surface for contacting the transducer to effect the transfer of ultrasonic energy to the chamber.

Abstract: A microbial membrane reactor for use in flow systems comprises a first element to receive the microorganisms and a second element to receive the flow channels. The two elements have planar interior surfaces which are pressed together separated by a membrane impervious to the microorganisms. The flow channels arranged in or on the surface of the second element serve to transport the liquid along the membrane so that the liquid can interact with the microorganisms arranged on the other side of the membrane. The geometry of the flow pathway and thus the geometry of the flow channels can be easily altered, in respect of the length, width and height of the channel, and adapted to practical requirements.

Abstract: There is provided a desulphurization apparatus to be mounted in automobiles, which is arranged between a fuel tank and an injector of an engine, the apparatus comprising a combination of a sulfur-containing compound adsorbent for adsorbing and concentrating the sulfur-containing compound and a sulfur-containing compound oxidizing agent or oxidation catalyst for oxidizing the adsorbed sulfur-containing compound, the apparatus further comprising a means for recovering and removing the resulting sulfur-containing oxide. According to this apparatus, the quantity of the particulate matter in an exhaust gas is reduced by half and the durability of the catalyst for removing a nitrogen oxide is improved by a factor of about two.

Abstract: A cell culture apparatus includes at least one growth support for cells which borders on at least one side to a culture medium compartment which is suppliable, preferably continuously, with liquid culture media via inflow and outflow openings. The cell culture apparatus includes at least one gas compartment which is suppliable with a defined gas or mixture of gases, wherein said gas compartment borders to the culture medium compartment via a gas permeable but liquid impermeable membrane.

Abstract: Disclosed is a bioreactor apparatus having a bed of buoyant media pellets floating within a filtrate to be processed. The apparatus includes a tank having a peripheral wall for containing filtrate and a bed of media pellets. A central manifold is rotatably supported within the tank the central manifold being mounted for rotation about a vertical axis and having a plurality of longitudinally spaced openings intermediate its ends, the openings adapted to eject filtrate in a generally horizontal direction and along a substantially vertical plane toward the wall of the tank. A thrust manifold, generally parallel to the axis of the central manifold has a plurality of longitudinally spaced openings intermediate its ends directed horizontally and generally perpendicularly to the plane. The thrust manifold is supported in association with the central manifold inwardly adjacent the tank wall and offset rearwardly of the plane to rotate with the central manifold.

Abstract: The present invention provides a miniaturized integrated nucleic acid diagnostic device and system. The device of the invention is generally capable of performing one or more sample acquisition and preparation operations, in combination with one or more sample analysis operations. For example, the device can integrate several or all of the operations involved in sample acquisition and storage, sample preparation and sample analysis, within a single integrated unit. The device is useful in a variety of applications, and most notably, nucleic acid based diagnostic applications and de novo sequencing applications.

Abstract: A cell-cultivating device includes a plurality of culture tanks and a driving device. The culture tanks communicate with each other and have culture medium inside. The driving device forces the culture medium to flow between the culture tanks so as to vertically oscillate medium levels in the culture tanks.

Abstract: The invention concerns a process for producing a three-dimensional bioartificial tissue having viable cells in or on a matrix, and by which cells and matrix can be cultivated into a tissue or a precursor of a tissue, a vascularized tissue of biological materials, obtained by this process, and an experimental reactor for scientific purposes and for producing clinically usable tissues and organs.

Abstract: A device for examining the sterility of fluids, in particular of pharmaceutical products is proposed. The device comprises a diaphragm filter inserted into a filtering unit for sterile filtration of the fluid, a collecting container which can be connected with the outlet of the filtering unit for the filtered matter and a container receiving at least one nutrition medium for incubation of the diaphragm filter to detect microorganisms. In accordance with the invention, the diaphragm filter can be inserted into and removed from the filtering unit by means of a handling device and be transferred by same, without contact, into the container receiving the nutrition medium such that, before incubation of the diaphragm filter, contamination of the diaphragm filter and of the nutrition medium is largely prevented to suppress erroneous positive results. The diaphragm filter preferably comprises a large surface and is substantially cylindrical, conical or tapered.

Abstract: A culture monitor (10) for microbiological testing of a liquid sample includes a housing having a liquid inlet (30) and a liquid outlet (32, 34), and a liquid sample filtration means inside the housing between the liquid inlet (30) and the liquid outlet (32, 34). The liquid sample filtration means including a filter medium (16) so that a liquid sample entering the housing through the liquid inlet (30) passes through the filter medium (16), with microorganisms present in the liquid sample being retained on the filter medium (16) and spent liquid or filtrate passing through the filter medium (16). A reservoir (53) is provided in the housing downstream of the liquid sample filtration means relative to the liquid inlet (30), with a volume of a rehydration agent for a dehydrated culture medium being provided in the reservoir (53), or the reservoir (53) being adapted to retain during filtration, as a rehydration agent, a portion of the filtrate.