Abstract: An organic light-emitting device comprising: an anode; a cathode; a first light-emitting layer between the anode and the cathode, the first light-emitting layer comprising a fluorescent light-emitting material having a triplet excited state energy level T1F and a triplet-triplet annihilation (TTA) promoter having a triplet excited state energy level T1T wherein T1F>1T; and a second light-emitting layer between the anode and the cathode and adjacent to the first light-emitting layer, the second light-emitting layer comprising a phosphorescent material having a triplet excited state energy level T1P wherein T1P>T1T.

Abstract: The present invention relates in general to microscopy systems. In particular, the present invention relates to microscopes rendering digital images of samples, with the capability to digitally control the focus of the microscope system, and the software used to control the operation of the digital microscope system. Further, the present invention relates to a microscope structure that allows for compact and multi-functional use of a microscope, providing for light shielding and control with samples that require specific light wavelength characteristics, such as fluorescence, for detection and imaging. The microscope is adjustable, with a structure that can move along range(s) of motion and degree(s) of freedom to allow for ease of access to samples, shielding of samples, and manipulation of a display apparatus.

Abstract: A tool and method for assisting in the maintenance and inspection of power lines by providing a platform that rides along the power lines.

Abstract: Provided are labeling reagents and methods for labeling primary antibodies and for detecting a target in a sample using an immuno-labeled complex that comprises a target-binding antibody and one or more labeling reagents. The labeling reagents comprise monovalent antibody fragments or non-antibody monomeric proteins whereby the labeling proteins have affinity for a specific region of the target-binding antibody and are covalently attached to a label. Discrete subsets of labeling reagent and immune-labeled complexes are provided that facilitate the simultaneous detection of multiple targets in a sample-complexes are distinguished by i) a ratio of label to labeling reagent, or ii) a physical property of said label, or iii) a ratio of labeling reagent to said target-binding antibody, or iv) by said target-binding antibody. This is particularly useful for fluorophore labels that can be attached to labeling reagents and subsequently immuno-labeled complexes in ratios for the detection of multiple targets.

Abstract: An analysis module accesses an input image, identifies an algorithm to be used to generate an output image from the input image, analyzes the algorithm, and determines a pixel offset of the algorithm. A generation module identifies a region of the output image in which output pixels are to be generated without an edge-checking operation. The generation module generates a modified version of the algorithm that omits the edge-checking operation and generates the output image by using the modified version to generate output pixels in the identified region.

Abstract: The present invention provides novel immunolabeling complexes and certain components of such complexes, as well as methods of preparing and using such complexes, and kits for use in preparing labeling proteins and for immunolabeling. The pre-formed immunolabeling complexes of the invention comprise both a target-binding antibody and a labeling protein that contains covalently attached labels, where the labeling protein binds selectively and with high affinity to a selected region of the target-binding antibody. Novel labeling proteins of the invention include non-antibody peptides and proteins, such as a complex of protein G and a labeled albumin, and monovalent antibody fragments, such as labeled Fab fragments of an anti-Fc antibody. In methods of the invention, the preformed immunolabeling complexes are added to the sample alone or in combination, for purposes of labeling and optionally detecting the target of interest.

Abstract: The present invention provides labeling reagents and methods for labeling primary antibodies and for detecting a target in a sample using an immuno-labeled complex that comprises a target-binding antibody and one or more labeling reagents. The labeling reagents comprise monovalent antibody fragments or non-antibody monomeric proteins whereby the labeling proteins have affinity for a specific region of the target-binding antibody and are covalently attached to a label. Typically, the labeling reagent is an anti-Fc Fab or Fab? fragment that was generated by immunizing a goat or rabbit with the Fc fragment of an antibody.

Abstract: An organic electronic device comprising: an anode; a hole injecting layer; a cathode; and organic semiconductive material disposed between the hole injecting layer and the cathode, wherein the cathode comprises an electron-injecting material having a higher electron-injection efficiency than BaO/Al, and wherein the hole injecting layer comprises a hole injecting material which has a lower workfunction than PEDOT:PSS (1:6).

Abstract: For standalone spreadsheet applications and/or Web-based spreadsheet services, the ability to designate, discover and set parameters for spreadsheet documents is provided. When creating a spreadsheet document, the ability to designate certain cells or ranges of cells as parameters to a spreadsheet is enabled. Furthermore, whether viewed in a standalone spreadsheet application or via a Web service, the ability to discover these parameters through the user interface or object model is provided. The ability to set or change these parameters one at a time or in bulk and drive the changes into the calculation model is also provided. Accordingly, whether viewed in a standalone spreadsheet application or via a Web rendering service, the effect of the parameters entered by the user can be calculated and viewed at once. The ability to suspend recalculation of a workbook until all relevant values, such as a current set of parameters, are obtained is also enabled.

Abstract: A method of forming an optical device comprising the steps of: providing a substrate comprising a first electrode capable of injecting or accepting charge carriers of a first type; forming over the first electrode a first layer that is at least partially insoluble in a solvent by depositing a first semiconducting material that is free of cross-linkable vinyl or ethynyl groups and is, at the time of deposition, soluble in the solvent; forming a second layer in contact with the first layer and comprising a second semiconducting material by depositing a second semiconducting material from a solution in the solvent; and forming over the second layer a second electrode capable of injecting or accepting charge carriers of a second type wherein the first layer is rendered at least partially insoluble by one or more of heat, vacuum and ambient drying treatment following deposition of the first semiconducting material.

Abstract: A method enables online purchase of customizable home construction plans. The method includes accessing a web based software package, customizing the home, and ordering the construction plans. The software package is a second aspect. The software allows the consumer to select different predefined features and add them to a stock floor plan. The selection of different features enables the customization of the home plan. The features selected are displayed to the consumer through a series of layers. The layers are superimposed on each other according to a predefined logic so that the consumer views what the home actually will look like rather an amalgamation of pieces. When the consumer is satisfied with the customized plan, the consumer orders formal plans and construction plans are sent to the consumer.

Abstract: The present invention provides labeling reagents and methods for labeling primary antibodies and for detecting a target in a sample using an immuno-labeled complex that comprises a target-binding antibody and one or more labeling reagents. The labeling reagents comprise monovalent antibody fragments or non-antibody monomeric proteins whereby the labeling proteins have affinity for a specific region of the target-binding antibody and are covalently attached to a label. Typically, the labeling reagent is an anti-Fc Fab or Fab? fragment that was generated by immunizing a goat or rabbit with the Fc fragment of an antibody.

Abstract: The present invention provides novel immunolabeling complexes and certain components of such complexes, as well as methods of preparing and using such complexes, and kits for use in preparing labeling proteins and for immunolabeling. The pre-formed immunolabeling complexes of the invention comprise both a target-binding antibody and a labeling protein that contains covalently attached labels, where the labeling protein binds selectively and with high affinity to a selected region of the target-binding antibody. Novel labeling proteins of the invention include non-antibody peptides and proteins, such as a complex of protein G and a labeled albumin, and monovalent antibody fragments, such as labeled Fab fragments of an anti-Fc antibody. In methods of the invention, the preformed immunolabeling complexes are added to the sample alone or in combination, for purposes of labeling and optionally detecting the target of interest.

Abstract: Barbecue grills, particularly small-size portable grills adapted for picnics, stadium parking lot cooking and the like. The portable grill comprises a hemispherical cooking bowl and a hemispherical hood removably supported upon the top rim of the cooking bowl. A pair of locking brackets is inserted within the cooking bowl rim, so as to engage the hood such, that the hood and cooking bowl are locked together during carrying.

Abstract: A stool seat includes an impermeable top wall having an upper surface upon which a user sits and a peripheral edge. The top wall is sealingly joined along its peripheral edge to an impermeable bottom wall and is adapted to support itself in spaced relation above the bottom wall so that the top wall is suspended above the bottom wall from its peripheral edge to provide a single sealed cavity containing a fluid at a predetermined pressure between the top and bottom walls. The top wall is further adapted to resiliently deflect toward the bottom wall under the weight of the user so that the pressure of the fluid in the sealed cavity is increased when the user sits upon the upper surface.

Abstract: An optically active 4-(4-substituted-2,6-dihydroxyphenyl)-6,6-dimethyl-2-norpinanone is reacted with a protonic acid to provide an optical isomer of a cis-1-hydroxy-3-substituted-6,6-dimethyl-6,6a,7,8,10,10a-hexahydro-9H-dibe nzo[b,d]pyran-9-one. Reaction of said norpinanone with a Lewis acid provides an optical isomer of trans-1-hydroxy-3-substituted-6,6-dimethyl-6,6a,7,8,10,10a-hexahydro-9H-di benzo[b,d]pyran-9-one. The optically active norpinanones are prepared by reaction of a 5-substituted-resorcinol with an optically active 6,6-dimethyl-2,4-diacetoxy-2-norpinene or an optically active 6,6-dimethyl-2,2-diacetoxy-3-norpinene, which compounds are derived from optically active .beta.-pinenes.

Abstract: Octahydro and hexahydrobenzo[b]cyclohepta[d]pyrans having the general formula ##STR1## wherein R.sup.1 is hydrogen or alkanoyl, R.sup.2 is alkyl or alkenyl, R.sup.3 is hydrogen or alkyl, and Z is a two carbon alkylene chain which is substituted or unsubstituted and saturated or unsaturated are provided. Pharmaceutical compositions containing such benzocycloheptapyrans, and a method of treating hypertension are disclosed.

Abstract: An optically active 4-(4-substituted-2,6-dihydroxyphenyl)-6,6-dimethyl-2-norpinanone is reacted with a protonic acid to provide an optical isomer of a cis-1-hydroxy-3-substituted-6,6-dimethyl-6,6a,7,8,10,10a-hexahydro-9H-dibe nzo[b,d]pyran-9-one. Reaction of said norpinanone with a Lewis acid provides an optical isomer of trans-1-hydroxy-3-substituted-6,6-dimethyl-6,6a,7,8,10,10a-hexahydro-9H-di benzo[b,d]pyran-9-one. The optically active norpinanones are prepared by reaction of a 5-substituted-resorcinol with an optically active 6,6-dimethyl-2,4-diacetoxy-2-norpinene or an optically active 6,6-dimethyl-2,2-diacetoxy-3-norpinene, which compounds are derived from optically active .beta.-pinenes.

Abstract: Octahydro and hexahydrobenzo[b]cyclohepta[d]pyrans having the general formula ##STR1## wherein R.sup.1 is hydrogen or alkanoyl, R.sup.2 is alkyl or alkenyl, R.sup.3 is hydrogen or alkyl, and Z is a two carbon alkylene chain which is substituted or unsubstituted and saturated or unsaturated are provided. Pharmaceutical compositions containing such benzocycloheptapyrans, and a method of treating hypertension are disclosed.

Abstract: 1-Hydroxy-9-keto-3-alkyl-dibenzo[b,d]pyrans or 1,9-dihydroxy-3-alkyl-dibenzo[b,d]pyrans are oxygenated on the penultimate carbon of the alkyl side chain by fermentation with a strain of the micro-organism Bacillus cereus.