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37 results about "Link protein" patented technology

Hyaluronan and proteoglycan link protein 1 is a protein that in humans is encoded by the HAPLN1 gene.. Interactions. HAPLN1 has been shown to interact with Versican.. References

Stabilized proteins

InactiveUS7037894B2Prevent undesired cross-linkControl cross-link reactionHormone peptidesPeptide/protein ingredientsTyrosineProtein retention
Isolated polypeptides or polypeptide chains are modified by di-tyrosine cross-linking such that the retain at least one functional activity. In one embodiment, the isolated polypeptide or polypeptide chains comprise at least one di-tyrosine cross-link, wherein at least one tyrosine of the di-tyrosine cross-link originates from a point mutation to tyrosine, and wherein the di-tyrosine cross-linked protein retains at least one function displayed by the protein in the absence of di-tyrosine cross-linking. In another embodiment, the di-tyrosine cross-linked polypeptide or polypeptide chain has enhanced stability compared to the same polypeptide or polypeptide chain in the absence of di-tyrosine cross-linking. A method for stabilization of a polypeptide or polypeptide complex, by the introduction of intra-polypeptide and / or inter-polypeptide di-tyrosine bonds, which simultaneously maintains the structure and function of the polypeptide or polypeptide complex is also described.
Owner:CALDER BIOSCI INC

Compositions and methods for entrapping protein on a surface

The present invention provides a formulation to link protein to a solid support that comprises one or more proteins, Oligo-dT and one or more non-volatile, water-soluble protein solvents, solutes or combination thereof in an aqueous solution. Further provided is a method of attaching a protein to a surface of a substrate. The formulations provided herein are contacted onto the substrate surface, printed thereon and air dried. The substrate surface is irradiated with UV light to induce thymidine photochemical crosslinking via the thymidine moieties of the Oligo-dT.
Owner:PURE TRANSPLANT SOLUTIONS L L C

Production process for separating and purifying fiber linking proteins from pig blood

The invention relates to a production process for separating and purifying fiber linking proteins from pig blood. The production process comprises the following steps: (1) separating blood plasma and blood cells from whole blood; (2) salting out: charging an acidic Na2HPO4-NaH2PO4 buffer solution into an upper layer of plasma, uniformly mixing, charging ammonium sulfate while stirring the solution so that the saturation degree reaches 20 percent, adjusting pH to be alkaline, placing the mixed solution into a refrigerator, refrigerating the mixed solution for 1.5 to 2.5 hours, sufficiently precipitating, finally centrifuging the solution, and obtaining a main precipitation component, i.e., fiber linking proteins; (3) dialyzing and desalting: dissolving precipitates in the step (2) into an acidic PBS buffer solution, putting the mixed solution into a dialysis bag, carrying out the dialysis and concentration, thereby obtaining a crude product of the fiber linking proteins; and (4) purifying: carrying out the affinity chromatography for an upper sample of the fiber linking protein crude product obtained in the step (3) by virtue of a gelatin sepharose-4B column, and eluting by virtue of a specific volume to obtain the purified fiber linking proteins. The production process is simple, low in requirement on needed equipment and suitable for industrialized production.
Owner:ANHUI BAODI MEAT FOODS

Methods of evaluating cells and cell cultures

Methods of evaluating the composition of a cell culture (e.g., to distinguish chondrocytes from fibroblasts) and methods for evaluating the phenotype of an individual cell (e.g., as a chondrocyte) are disclosed. The methods may be used, for example, for assessing chondrocyte cultures used for treatment of cartilage defects. In some embodiments, the invention involves identifying cell culture composition or the identity of a cell based on expression level of a fibroblast marker. In other embodiments, the invention involves comparing expression levels of at least one chondrocyte marker and at least one fibroblast marker in a cell culture sample or in an individual cell. In illustrative embodiments, the chondrocyte marker is hyaluronan and proteoglycan link protein 1 (HAPLN1), and the fibroblast marker is microfibrillar associated protein 5 (MFAP5).
Owner:GENZYME CORP

Methods and Products for Fusion Protein Synthesis

The present invention provides a method of producing a fusion protein, said method comprising: a) contacting a first protein with a second protein under conditions that enable the formation of an isopeptide bond between said proteins, wherein said first protein and said second protein each comprise a peptide linker, wherein said peptide linkers are a pair of peptide linkers which react to form an isopeptide bond that links said first protein to said second protein to form a linked protein; and b) contacting the linked protein from (a) with a third protein under conditions that enable the formation of an isopeptide bond between said third protein and said linked protein, wherein said third protein comprises a peptide linker which reacts with a further peptide linker in the linked protein from (a), and wherein said peptide linkers are a pair of peptide linkers that react to form an isopeptide bond that links said third protein to said linked protein to form a fusion protein, wherein said pair of peptide linkers used in (a) are orthogonal to the pair of peptide linkers used in (b). Peptide linkers and the use of orthogonal pairs of said linkers in the synthesis of fusion proteins are also provided. Recombinant proteins comprising said linkers, nucleic acid molecules encoding said proteins and linkers, vectors comprising said nucleic acid molecules and host cells comprising said vectors and nucleic acid molecules are also contemplated.
Owner:OXFORD UNIV INNOVATION LTD

Polypeptide-human protein containing linking protein family characteristic sequential fragment-9.68 and polynucleotide for encoding it

A polypeptide-human protein-9.68 containing vinculin family characteristic sequence fragment, the polynucleotide for coding it, the process for preparing said polypeptide by DNA recombination, the application of said polypeptide in treating diseases such as digestive ulcer, diabetes, etc, the antagonist of said polypeptide and its medical action, and the application of said polynucleotide are disclosed.
Owner:FUDAN UNIV +1

Microcapsule slow-releasing seed coating agent for efficiently preventing and treating clubroots of oilseed rapes

The invention discloses a microcapsule slow-releasing seed coating agent for efficiently preventing and treating clubroots of oilseed rapes. The microcapsule slow-releasing seed coating agent is characterized by being prepared from, by weight, 10 parts to 15 parts of medicine-containing microcapsules, 1 part to 10 parts of film forming agents, 1 part to 10 parts of dispersing agents and 100 parts to 110 parts of assistants; in the medicine-containing microcapsules, the weight ratio of medicine to microcapsule materials is 1:5 to 10; the medicine comprises at least one kind of 6% oligosaccharide.link proteins, Pulvtong and 3% extremely-thin alternaria alternate activator proteins; the microcapsule materials comprise one kind of polylactic acid, polypropylene carbonate and chitosan-lactide copolymers; the medicine-containing microcapsules are prepared with an emulsified solvent evaporation method; the medicine-containing microcapsules, the film forming agents, the dispersing agents and the assistants are mixed to be grinded into particles with the size smaller than or equal to 5 micrometers, and the microcapsule slow-releasing seed coating agent is obtained. The preventing and treating effect of the microcapsule slow-releasing seed coating agent on the clubroots of the oilseed rapes is higher than 90%, and preventing and treating time is longer than eight weeks; the microcapsule slow-releasing seed coating agent is free of damage to the environment and injuries to health of people and livestock and easy to apply, and has good market application prospects.
Owner:INST OF PLANT PROTECTION SICHUAN ACAD OF AGRI SCI
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