| Class / Patent application number | Description | Number of patent applications / Date published |
|---|
| 435207000 | Acting on beta-galatose-glycoside bond (e.g., beta-galactosidase, etc.) | 6 |
| 20110003362 | Conjugates of biological substances - Chemically reactive carbocyanine dyes that are intramolecularly crosslinked between the 1-position and 3′-position, their bioconjugates and their uses are described. 1,3′-crosslinked carbocyanines are superior to those of conjugates of spectrally similar 1,1′-crosslinked or non-crosslinked dyes. The invention includes derivative compounds having one or more benzo nitrogens. | 01-06-2011 |
| 20110212505 | BGL3 Beta-Glucosidase and Nucleic Acids Encoding the Same - The present invention provides a novel β-glucosidase nucleic acid sequence, designated bgl3, and the corresponding BGL3 amino acid sequence. The invention also provides expression vectors and host cells comprising a nucleic acid sequence encoding BGL3, recombinant BGL3 proteins and methods for producing the same. | 09-01-2011 |
| 20130224833 | Method for Preparing and Using Cell Extract Solution for Tubulin-free Cell-free Protein Synthesis and Reagent Kit for Cell-free Protein Synthesis - A method is provided for preparing cell extract solution for cell-free protein synthesis that can effectively remove tubulin protein, a reagent kit for cell-free protein synthesis including the extract solution, and a method for synthesizing cell-free protein using the extract solution. The method for preparing cell extract solution for cell-free protein synthesis includes the steps of: obtaining an extraction treated material of cultured cells by subjecting the cultured cells to an extraction treatment using an extraction buffer; obtaining a reaction mixture by subjecting the extraction treated material to tubulin polymerization reaction and polymerizing the tubulin derived from the culture cells included in the extraction treated material; and preparing the cell extract solution for cell-free protein synthesis by subjecting the reaction mixture to removal of the polymerized tubulin and a buffer exchange. | 08-29-2013 |
| 20140057335 | CULTURE MEDIUM FOR CELL GROWTH AND TRANSFECTION - The present invention is directed generally to cell culture media useful for introducing macromolecules and compounds (e.g., nucleic acid molecules) into cells (e.g., eukaryotic cells in the presence of said media. Cells containing introduced materials can be further cultured in the media. In particular, the invention allows introduction of nucleic acid molecules (e.g., vectors) into cells (particularly eukaryotic cells) and expression of proteins encoded by the nucleic acid molecules in the cells. The invention obviates the need to change the cell culture medium each time a different procedure is performed with the cells (e.g., culturing cells vs. transfecting cells). The invention thus provides efficient and high throughput methods to transform/transfect culture and cells avoiding the need for multiple manipulations and transfers of cells during transfection and expression studies. | 02-27-2014 |
| 20140113350 | METHOD FOR KILLING MICROORGANISM - Provided is a technique for enabling a liquid of microbial cells having an enzymatic activity to be easily stored and used. The technique is a method for killing a microorganism while maintaining the enzyme titer of a microbial cell liquid, characterized by including adjusting the pH of a liquid of microbial cells having an enzymatic activity, and then performing a heating treatment of the liquid, and also the technique is a method for killing a microorganism while maintaining the enzyme titer of a microbial cell liquid, characterized by including adding a carbohydrate to a liquid of microbial cells having an enzymatic activity, and then performing a heating treatment of the liquid. | 04-24-2014 |
| 20140234942 | SUBSTRATES AND METHODS FOR COLLECTION, STABILIZATION AND ELUTION OF BIOMOLECULES - A solid substrate for the extraction, stabilization, and storage of proteins is provided. The substrate includes: a polysaccharide, such as melezitose under a substantially dry state. The substrate is configured to extract proteins from a sample and stabilize the extracted proteins in a dry format under ambient conditions for a prolonged period of time. Methods for collecting and recovering the proteins stored in the dry solid substrate are also described. | 08-21-2014 |
