序号 专利名 申请号 申请日 公开(公告)号 公开(公告)日 发明人
121 METHODS FOR MANUFACTURING MOLECULAR ARRAYS EP12843117.8 2012-10-26 EP2771450A1 2014-09-03 ROUTENBERG, David, A.
The methods of the present invention provide methods for manufacturing a master substrate and methods for manufacturing replica arrays from the master substrate. The methods may be used, for example, directly to manufacture or "print" peptide arrays from a DNA array; however, the methods are applicable to a wide range of manufacturing applications for use any time multiple copies of an array needs to be printed.
122 Sensing device and manufacturing method thereof EP10161670.4 2010-04-30 EP2388337B1 2014-07-02 Van Steenwinckel, David; Frederix, Filip
123 Reactor assembly EP10182340.9 2002-05-13 EP2263790B1 2014-04-16 Van den Brink, Peter John; Bracht, Maarten; Gruter, Gerardus Johannes Maria; De Ruiter, René; Harji, Bashir Husein
124 METHOD OF DETERMINING, IDENTIFYING OR ISOLATING CELL-PENETRATING PEPTIDES EP12789086.1 2012-05-23 EP2714971A1 2014-04-09 WATT, Paul Michael; HOPKINS, Richard; HOFFMAN, Katrin
The present invention provides a method of determining or identifying or isolating a cell-penetrating peptide (CPP) or analog or derivative thereof having cell-type selectivity and/or at least capable of passing through a Blood Brain Barrier of an animal subject. This invention also provides CPPs and analogs and derivatives thereof, such as those set forth in SEQ ID NOs: 1-27 of the Sequence Listing, and compositions comprising one or more of the CPPs, including conjugates in which a CPP or analog or derivative thereof is linked to a cargo molecule. The invention also provides methods for transporting cargo molecules across cell membranes to specific locations within cells, and for treating, preventing and/or diagnosing diseases that are treatable by a cargo molecule to which a CPP or analog or derivative of the invention is attached. The invention also provides tailored peptide libraries for use in identifying or isolating CPPs.
125 FLUORESCENCE SCANNING HEAD WITH MULTIBAND DETECTION EP12776158.3 2012-04-30 EP2702394A1 2014-03-05 McCOLLUM, Tom
In a scanning system for the detection and discrimination of a plurality of targets in each of a plurality of samples, one or more multiband fluorescence detection channels each of which contains a single multiband emission filter and a single detector replaces multiple detection components in scanning heads of the prior art. In certain embodiments, a single multi-emitter light source is used as well, to illuminate each sample with excitation light at a variety of distinct wavelengths in succession.
126 DIAGNOSTIC AND TREATMENT METHODS USING A LIGAND LIBRARY EP12760047.6 2012-03-23 EP2689053A2 2014-01-29 MOOLA, Muralidhar, Reddy; SCHILKE, Jessica
The present invention is useful in screening for biomarkers associated with any other disease or condition. Such diseases and conditions range from the neurological diseases, autoimmune diseases and cancers identified above as well as any other disease or condition that has a biomarker such as an antibody or other characterizing protein or biomolecule associated with the disease or progression of the disease. The large ligand libraries of the invention can be used directly in biological fluid, under the appropriate experimental conditions and according to the processes recited herein, to screen for such markers and without the need to use fewer support members (e.g. about 100,000 or less) or without the need to transfer such peptoids or ligands to a microarray before screening the biological fluid. In addition, the ligand libraries may also be used to screen for cell based receptors that specifically relate to a particular cell surface marker.
127 SYSTEMS AND METHODS FOR HIGH-THROUGHPUT DETECTION OF AN ANALYTE IN A SAMPLE EP12755510.0 2012-03-09 EP2684036A2 2014-01-15 OSTERFELD, Sebastian J.; WANG, Shan X.
Provided are high-throughput detection systems. The systems include a magnetic sensor device, a magnetic field source and a reservoir plate that includes a plurality of fluid reservoirs. The magnetic sensor device includes a support with two or more elongated regions each having a magnetic sensor array disposed at a distal end. Also provided are methods in which the subject high-throughput detection systems find use.
128 ANALYSIS METHOD AND READING DEVICE FOR MICROARRAY EP11857286.6 2011-12-26 EP2669662A1 2013-12-04 OZAKI, Kumie; SASAMOTO, Hiromichi; NAGINO, Kunihisa

In order to provide a microarray analysis method that can perform alignment processing appropriately in an analysis of a DNA chip on which no positive control is arranged or an analysis of a chip on which a sample contains a small amount of DNAs, the microarray analysis method in which a microarray obtained by arranging probes on a substrate surface having an irregular shape is irradiated with excitation light and fluorescence amounts of the probes excited by the excitation light are obtained as numerical data includes a step (a) of measuring the fluorescence amounts of the probes to acquire fluorescence image data, a step (b) of receiving reflected light and/or scattered light from the substrate surface to acquire the irregular shape of the substrate surface of the microarray as alignment image data based on the light receiving intensities of the light, and a step (c) of determining positions of the probes on the fluorescence image data based on the alignment image data.

129 A MEMBRANE BASED MICROARRAY DEVICE FOR HIGH-THROUGHPUT MULTIANALYTE DETECTION EP10735276.7 2010-07-21 EP2457094A1 2012-05-30 LEGOFF, Gaëlle; BRES, Jean-Charles; MARQUETTE, Christophe; RIGAL, Dominique; BLUM, Loïc
A device – for performing an assay-comprising a substantially rigid support forming at least one well defining an inner cavity, having a bottom wall provided with a hole, a porous membrane sealed onto the support closing said hole and having an inner surface oriented towards the inside of the cavity and an opposite outer surface, at least one probe embedded within the porous membrane so as to immobilize the probe within the membrane.
130 Microfluidic Devices And Methods Of Use In The Formation And Control Of Nanoreactors EP10196179.5 2006-06-01 EP2364774A2 2011-09-14 LINK, Darren, R.; BOITARD, Laurent; BRANCIFORTE, Jeffrey; CHARLES, Yves; FEKE, Gilbert; LU, John, Q.; MARRAN, David; TABATABAI, Ahmadali; WEINER, Michael; HINZ, Wolfgang; ROTHBERG, Jonathan, M.

The present invention provides novel microfluidic devices and methods that are useful for performing high-throughput screening assays and combinatorial chemistry. Such methods can include labeling a library of compounds by emulsifying aqueous solutions of the compounds and aqueous solutions of unique liquid labels on a microfluidic device, which includes a plurality of electrically addressable, channel bearing fluidic modules integrally arranged on a microfabricated substrate such that a continuous channel is provided for flow of immiscible fluids, whereby each compound is labeled with a unique liquid label, pooling the labeled emulsions, coalescing the labeled emulsions with emulsions containing a specific cell or enzyme, thereby forming a nanoreactor, screening the nanoreactors for a desirable reaction between the contents of the nanoreactor, and decoding the liquid label,; thereby identifying a single compound from a library of compounds.

131 Microfluidic Devices And Methods Of Use In The Formation And Control Of Nanoreactors EP10196339.5 2006-06-01 EP2363205A2 2011-09-07 LINK, Darren, R.; BOITARD, Laurent; BRANCIFORTE, Jeffrey; CHARLES, Yves; FEKE, Gilbert; LU, John, Q.; MARRAN, David; TABATABAI, Ahmadali; WEINER, Michael; HINZ, Wolfgang; ROTHBERG, Jonathan, M.

The present invention provides novel microfluidic devices and methods that are useful for performing high-throughput screening assays and combinatorial chemistry. Such methods can include labeling a library of compounds by emulsifying aqueous solutions of the compounds and aqueous solutions of unique liquid labels on a microfluidic device, which includes a plurality of electrically addressable, channel bearing fluidic modules integrally arranged on a microfabricated substrate such that a continuous channel is provided for flow of immiscible fluids, whereby each compound is labeled with a unique liquid label, pooling the labeled emulsions, coalescing the labeled emulsions with emulsions containing a specific cell or enzyme, thereby forming a nanoreactor, screening the nanoreactors for a desirable reaction between the contents of the nanoreactor, and decoding the liquid label,; thereby identifying a single compound from a library of compounds.

132 SERS-BASED, SINGLE STEP, REAL-TIME DETECTION OF PROTEIN KINASE AND/OR PHOSPHATASE ACTIVITY EP08869885 2008-12-23 EP2227681A4 2011-01-12 CHEN FANQING FRANK; LIU GANG L; ELLMAN JONATHAN A
133 HIGH PRESSURE PARALLEL FIXED BED REACTOR AND METHOD EP07854450 2007-10-26 EP2104755A4 2011-01-12 BERGH H SAM; WELLS JASON; WONG VICTOR; GALLIPEO JOHN; VAN ERDEN LYNN; VOLPE ANTHONY F; MAAG JEFFREY
134 Reactor assembly EP10182340.9 2002-05-13 EP2263790A3 2011-01-05 Van den Brink, Peter John; Bracht, Maarten; Gruter, Gerardus Johannes Maria; De Ruiter, René; Harji, Bashir Husein

The invention relates to a reactor assembly for analyzing the effluent streams from a plurality of flow-through reactors, comprising:

- a plurality of flow-through reactors for performing chemical reactions, each reactor comprising:

- a reaction chamber (1), comprising a reaction zone (2), the reaction chamber being connected to

- at least one reactor inlet (3) for at least one reactant, upstream of the reaction zone,

- at least one reactor outlet (4) for the effluent stream from the reaction zone, downstream of the reaction zone,



- a housing comprising a base block and a cover element,

wherein the base block (5) comprises a plurality of first channels (6), each first channel accommodating a flow-through reactor and a second sealing element (12), arranged between the outside of the reactor and the inner wall of the fist channel,



wherein the reactor assembly further comprises:

- at least one analyzer for subjecting the effluent stream to an analyzing procedure, each reactor outlet being connected to at least one analyzer by an effluent conduit, and

- at least one dilution gas supply means (16), for adding at least one dilution gas to the effluent stream, downstream of the reaction zone,



characterized in that,

a space (14) is present in each first channel between the outer wall of the reactor and the inner wall of the first channel and below the second sealing element (12),

and in that the base block comprises fourth channels, each fourth channel being connected to a first channel and opening in said space (14) in that first channel below the second sealing element and above the reactor outlet for adding a dilution gas to the effluent stream of the reactor arranged in said first channel.

135 SERS-BASED, SINGLE STEP, REAL-TIME DETECTION OF PROTEIN KINASE AND/OR PHOSPHATASE ACTIVITY EP08869885.7 2008-12-23 EP2227681A2 2010-09-15 CHEN, Fanqing, Frank; LIU, Gang, L.; ELLMAN, Jonathan, A.
This invention provides novel compositions and methods for the detection, and/or quantification, of the presence and/or activity of one or more kinases and/or phosphatases. In certain embodiments this invention a device for the detection of kinase and/or phosphatase activity where the device comprises a Raman active surface comprising features that enhance Raman scattering having attached thereto a plurality of kinase and/or phosphatase substrate molecules.
136 OPTICAL PROBES AND ASSAYS FOR MEASURING PROTEIN PHOSPHORYLATION EP00932098.7 2000-05-05 EP1175508B1 2007-07-25 POLLOK, Brian, A.; HAMMAN, Brian, D.; RODEMS, Steven, M.; MAKINGS, Lewis, R.
This invention provides an optical probe useful as an optical probe or sensor of post translational type modifications, such as phosphorylation. The invention comprises a polypeptide moiety, which contains a recognition motif for a post translational type activity, and a protease site, which is coupled to a probe moiety. Modification of the polypeptide, by the post translational type activity, results in a modulation of the rate at which a protease cleaves the polypeptide which is sensed by a measurable change in at least one optical property of the optical probe upon cleavage. The present invention also includes a recombinant nucleic acid molecule that encodes an optical probe and a vector and host cell or library of cells that include the recombinant nucleic acid molecule. The optical probe can be used in methods to determine whether a sample, including a cell or a sample from an organism, contains a post-translational type modification activity. Such methods can also be used to determine whether a test chemical modulates the activity of a modifying activity, and thus can be used to identify therapeutic compositions. The identification of such therapeutic compositions can be automated using a system that includes an optical probe.
137 Infrared spectroscopy and imaging of libraries EP06004658.8 1997-10-07 EP1669738A2 2006-06-14 McFarland, Eric, W.; Archibald, William

A method of characterizing materials comprising the steps of: providing a substrate; synthesizing an array of materials on said substrate; providing at least one reactant gas wherein said reactant gas is in contact with said array of materials; activating at least one of said materials on said array with a heating source; and periodically monitoring an infrared emission from said activated material with an infrared camera, wherein said infrared camera outputs a series of signals corresponding to an emission intensity varying with time of said activated material.

138 A conduit system for mass spectrometers and methods for rapid screening of libraries of different materials EP02018112.9 1997-10-08 EP1280185A1 2003-01-29 Weinberg, W. Henry; McFarland, Eric W.; Cong, Peijun; Guan, Shenheng

A conduit system for an apparatus for screening materials is provided, wherein the conduit system comprises a sampling probe having an inner passage and an outer passage concentrically arranged around the inner passage. Moreover, a screening apparatus including the conduit system and a method of operating the apparatus are provided.

139 Apparatus, suitable for high throughput experimentation EP01201739.8 2001-05-11 EP1256377A1 2002-11-13 Bracht, Maarten

Apparatus suitable for high throughput experimentation, comprising an assembly (1) for housing at least one vessel (2) having a first and second vessel opening (3, 4), the assembly (1) comprising:

  • a base block (5) having at least one through going first channel (6) for removably housing the vessel (2), having a first channel opening (19), opening in a first face (7) of the block, and a second channel opening (18), opening in a second face (8) of the block (5);
  • a cover element (9) with the bottom surface (10) facing the base block (5) being releasably attached to the first face (7) thereof;
  • a first sealing element (11) between the first face (7) of the base block (5) and the bottom surface (10) of the cover element (9), being placed such that it seals gastight around said first channel opening (19) between the cover element (9) and the base block (5); and
  • a second sealing element (12) located in the first channel (6) around the vessel (2), sealing gastight against the inside of the first channel (6) and the outside of the vessel (2).

140 MASS SPECTROMETERS AND METHODS FOR RAPID SCREENING OF LIBRARIES OF DIFFERENT MATERIALS EP97910017.9 1997-10-08 EP1019947B1 2002-08-14 WEINBERG, W., Henry; MCFARLAND, Eric, W.; CONG, Peijun; GUAN, Shenheng
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