Abstract:
The invention is a composition comprising a curable arylcyclobutene based oligomer or polymer and a dissolution inhibitor which comprises a compound comprising at least two diazonaphthoquinone (DNQ) moieties each of which is pendant from different phenyl groups.
Abstract:
The invention discloses a method for improving the cooking and eating quality of brown rice by using Lactic acid bacteria fermentation, which belongs to the technical field of food processing. The method comprises the steps of mixing activated lactic acid bacteria with water and brown rice, loading the mixture into a one-way outgassing container, removing excess air or filling up the container, and sealing the container and performing fermentation. The invention is very simple and easy to operate, and has very low energy consumption. It is suitable to be up scaled for industrial production and will significantly promote brown rice to become a staple food.
Abstract:
Disclosed is a lipophilic agent comprising a triazine core having lipophilic groups for organic synthesis. The lipophilic agent soluble in one system of solvent(s) wherein the lipophilic agent is participated in a chemical reaction but insoluble by adding a miscible poor solvent to change solution composition after the reaction completes. The lipophilic agent facilitates process improvement wherein practical operation only involves mixing with reactants in solution followed by precipitating with change of solution composition followed by filtering to obtain the precipitated solid, simplifying the purification by isolating the desired solid. The operation is reproducible along the progress in a multi-step synthesis, allowing pure intermediates and pure product as a solid to be rapidly obtained with ease and certainty. This invention can thus accelerate research and development of pharmaceutical biomolecules, representing a tremendous step forward for boosting productivity and greening chemical industry.
Abstract:
FIG. 1 is a front, right and top perspective view of a sunshade, showing my design. FIG. 2 is a rear, left and bottom perspective view thereof. FIG. 3 is a front elevation view thereof. FIG. 4 is a rear elevation view thereof. FIG. 5 is a left side elevation view thereof. FIG. 6 is a right side elevation view thereof. FIG. 7 is a top plan view thereof. FIG. 8 is a bottom plan view thereof. FIG. 9 is an enlarged view of detail 9 in FIG. 1. FIG. 10 is an enlarged view of detail 10 in FIG. 2. FIG. 11 is an enlarged view of detail 11 in FIG. 2; and, FIG. 12 is an enlarged view of detail 12 in FIG. 2. The broken lines depict portions of the sunshade that form no part of the claimed design. The dot-dash broken lines in FIGS. 1, 2, 9, 10, 11 and 12 depict the boundaries of the enlargements that form no part of the claimed design.
Abstract:
The invention relates to novel fluorescent dyes based on the following pyrenyloxy sulfonamide structure: wherein R1 is a leash joined to the pyrenyloxy group via an ether link containing generally a reactive functional group such as, activated carbonate, activated ester, amino group, azide or alkyne for conjugation with biomolecules; R2 and R3 are hydrogen atoms, or short alkyl chains, or cyclic rings with or without heteroatoms such as nitrogen, oxygen, sulfur, phosphorus. The spectral properties of the fluorescent dyes are sufficiently different in wave-lengths and intensity from fluorescein as to permit simultaneous use of fluorescein and/or more other fluorescent dyes with minimum interference and to avoid interference from endogenous green fluorescent protein in biological system. The dyes are non-ionic to facilitate their entry into cells for intracellular detection. The non-ionic structure also precludes undesired electrostatic reactions with ionic sites on biological components and structures. The dyes have bigger Stokes' shifts than other dyes with similar spectral properties allowing use of simpler, more efficient detection equipment, are not sensitive to pH, and have good solubility in aqueous solution.
Abstract:
A compound useful in the formation of polymeric dielectric films for semiconductor devices and the resulting cured films and devices, said compound comprising i) three or more dienophile groups (A-functional groups) and ii) a single ring structure comprising two conjugated carbon-to-carbon double bonds and a leaving group L (collectively referred to as a B-functional group), characterized in that one A-functional group of one molecule of the compound is capable of reaction under cycloaddition reaction conditions with the B-functional group of a second molecule and elimination of the leaving group L, to thereby form a polymer.
Abstract:
FIG. 1 is a front, right and top perspective view of a sunshade, showing my design. FIG. 2 is a rear, right and bottom perspective view thereof. FIG. 3 is a rear, right and top perspective view thereof. FIG. 4 is a front elevation view thereof. FIG. 5 is a rear elevation view thereof. FIG. 6 is a left side elevation view thereof. FIG. 7 is a right side elevation view thereof. FIG. 8 is a top plan view thereof. FIG. 9 is a top plan view thereof. FIG. 10 is an enlarged view of detail 10 in FIG. 1. FIG. 11 is an enlarged view of detail 11 in FIG. 2; and, FIG. 12 is an enlarged view of detail 12 in FIG. 2. The broken lines depict portions of the sunshade that form no part of the claimed design. The dot-dash broken lines in FIGS. 1, 2 10, 11 and 12 depict the boundaries of the enlargements that form no part of the claimed design.
Abstract:
The invention relates to novel fluorescent dyes based on the following pyrenyloxy sulfonamide structure: wherein R1 is a leash joined to the pyrenyloxy group via an ether link containing generally a reactive functional group such as, activated carbonate, activated ester, amino group, azide or alkyne for conjugation with biomolecules; R2 and R3 are hydrogen atoms, or short alkyl chains, or cyclic rings with or without heteroatoms such as nitrogen, oxygen, sulfur, phosphorus. The spectral properties of the fluorescent dyes are sufficiently different in wave-lengths and intensity from fluorescein as to permit simultaneous use of fluorescein and/or more other fluorescent dyes with minimum interference and to avoid interference from endogenous green fluorescent protein in biological system. The dyes are non-ionic to facilitate their entry into cells for intracellular detection. The non-ionic structure also precludes undesired electrostatic reactions with ionic sites on biological components and structures. The dyes have bigger Stokes' shifts than other dyes with similar spectral properties allowing use of simpler, more efficient detection equipment, are not sensitive to pH, and have good solubility in aqueous solution.
Abstract:
Morpholino antisense oligos (Morpholinos) are a class of synthetic non-ionic molecules, each designed to very specifically bind to a selected complementary RNA sequence (targeted RNA transcript). Custom-sequence Morpholinos are used in a broad range of biological research areas, as well as for therapeutic applications in vivo (in living animals such as humans). For most in vivo applications the “bare” Morpholino (FIG. 1a) is linked to a cationic delivery component to give a “delivery-enabled” Morpholino (FIG. 1b) with significantly improved delivery efficiency. However, cytosolic delivery was still markedly less than expected. Then recently we discovered that by adding a special disconnect component between the Morpholino component and the cationic delivery component (FIG. 1c), the cytosolic delivery efficiency for the Morpholino was dramatically increased (about a 1,000% increase in delivery efficiency). This patent application describes designing, making, and using such delivery-enabled Morpholinos containing a key disconnect component.
Abstract:
FIG. 1 is a front, right and top perspective view of a sunshade, showing my design. FIG. 2 is a rear, left and bottom perspective view thereof. FIG. 3 is a rear, left and top perspective view thereof. FIG. 4 is a front elevation view thereof. FIG. 5 is a rear elevation view thereof. FIG. 6 is a left side elevation view thereof. FIG. 7 is a right side elevation view thereof. FIG. 8 is a top plan view thereof. FIG. 9 is a bottom plan view thereof. FIG. 10 is an enlarged view of detail 10 in FIG. 1. FIG. 11 is an enlarged view of detail 11 in FIG. 1. FIG. 12 is an enlarged view of detail 12 in FIG. 2; and, FIG. 13 is an enlarged view of detail 13 in FIG. 2. The broken lines depict portions of the sunshade that form no part of the claimed design. The dot-dash broken lines in FIGS. 1, 2 10, 11 and 12 depict the boundaries of the enlargements that form no part of the claimed design.