Patent application number | Description | Published |
20130115609 | Methods and Kits for Detecting Circulating Cancer Stem Cells - Disclosed herein is the use of LIN28B gene or a variant thereof as a cancer stem cell marker gene for the diagnosis, treatment, or prognosis of a malignant tumor such as hepatocellular carcinoma. Also included herein are methods and kits for detecting circulating cancer stem cells in a subject. According to various embodiments of the disclosure, the methods and kits use the LIN28B gene or a variant thereof as the cancer stem cell marker gene. | 05-09-2013 |
20130121664 | SYNOPSIS FRAMES AND MANUFACTURING METHOD THEREOF - A synopsis video includes a plurality of synopsis frames manufactured by using plural chronological source frames which include a plurality of foreground objects. Each of the foreground objects appearing in one of the synopsis frames just exists at one position of the synopsis frame. At least one portion of the foreground objects appearing in one of the synopsis frames originates from the source frames of different times. One of the foreground objects that originates from a later source frame appears in a later synopsis frame, and the foreground object that originates from a former source frame appears in a former synopsis frame. | 05-16-2013 |
20130128356 | Metallic Structure and Opto-Electronic Apparatus - A metallic structure and an opto-electronic apparatus are provided. The metallic structure is used for filtering or polarizing an electromagnetic wave, and includes a light-permissible medium, a first metallic block and a second metallic block. The first and second metallic blocks are parallel to and spaced from each other at a predetermined distance (d), and are disposed inside or over the light-permissible medium. After passing through the metallic structure, the electromagnetic wave has a distribution curve of transmittance versus wavelength, wherein the distribution curve has at least one transmittance peak value corresponding to at least one wavelength in a one-to-one manner. The aforementioned predetermined distance (d) and an averaged width of the first metallic block satisfy the following relationships: d<λ; 0.01λ05-23-2013 | |
20130129744 | PLASMINOGEN-ACTIVATING ANTIBODY, USE AND PRODUCING METHOD THEREOF AND AGENT INCLUDING THE SAME - An antibody for activating plasminogen is provided. The antibody is produced from a hybridoma cell line deposited on Nov. 24, 2011 under accession number BCRC 960433 at Food Industry Research and Development Institute, 331 Shih-Pin Road, Hsinchu 300, Taiwan. The uses and producing method of the antibody, and an agent including the antibody used for treating stroke, myocardial infarction or syndromes cause by thrombus are also disclosed. | 05-23-2013 |
20130146918 | Yttrium aluminum garnet phosphor, method for preparing the same, and light-emitting diode containing the same - The present invention relates to yttrium aluminum garnet phosphor, a method of preparing the same and a light-emitting diode containing the same. The yttrium aluminum garnet phosphor of the present invention is represented by the following formula (I): | 06-13-2013 |
20130148074 | LIQUID CRYSTAL LIGHT VALVE AND METHOD FOR MANUFACTURING THE SAME - The present invention relates to a liquid crystal light valve comprising: a first substrate where a first polymer layer is formed thereon; a second substrate where a second polymer layer is formed thereon, the first polymer layer is opposite to the second polymer; and a liquid crystal material layer filled in between the first polymer layer and the second polymer layer, wherein the first polymer layer and the second polymer layer have a roughened surface, and the roughened surface is disposed between the first polymer layer and the liquid crystal material layer, or between the second polymer layer and the liquid crystal material layer. | 06-13-2013 |
20130149702 | PRIMER SET, METHOD AND KIT FOR DETECTING PATHOGEN IN FISH - The invention provides a method for rapidly detecting a pathogen in fish comprising conducting loop-mediated isothermal amplification with a specific primer set and a nucleic acid in a test sample. If at least one amplification is carried out, the test sample comprises the pathogen in fish. The invention also provides a primer set, probe and kit for detecting a pathogen in fish. | 06-13-2013 |
20130159226 | Method for Screening Samples for Building Prediction Model and Computer Program Product Thereof - A method for screening samples for building a prediction model and a computer program product thereof are provided. When a set of new sample data is added to a dynamic moving window (DMW), a clustering step is performed with respect to all of the sets of sample data within the window for grouping the sets of sample data with similar properties as one group. If the number of the sets of sample data in the largest group is greater than a predetermined threshold, it means that there are too many sets of sample data with similar properties in the largest group, and the oldest sample data in the largest group can be deleted; if smaller than or equal to a predetermined threshold, it means that the sample data in the largest group are quite unique, and should be kept for building or refreshing the prediction model. | 06-20-2013 |
20130162086 | PERMANENT MAGNET APPARATUS - A permanent magnet apparatus includes a rotor structure and a stator structure. The rotor structure has a first permeance element and a plurality of first magnetic elements. The outer periphery of the first permeance element has a plurality of grooves which are disposed separately. The first magnetic elements are disposed correspondingly in the grooves. The stator structure is disposed at the outer periphery of the rotor structure, and includes a second permeance element and a plurality of second magnetic elements around the rotor structure. | 06-27-2013 |
20130180855 | CAPILLARY ELECTROPHORESIS METHOD FOR ANALYZING COLLAGEN - A capillary electrophoresis method for identification and analyzing collagen quantitatively, which is used to identify and quantify collagen in a sample, comprises the steps of: (a) dissolving a collagen-containing sample to form a sample solution; (b) preparing a capillary with an inner wall thereof having a positively-charged layer; (c) introducing the sample solution into the capillary filled with an analytical buffer solution; and (d) driving the sample solution to pass through the capillary. The method of the present invention does not need the purifying pre-treatment and cracking the collagen-containing sample but directly performs the capillary electrophoresis analysis of collagen. Therefore, the present invention can shorten the time for analyzing collagen quantitatively. | 07-18-2013 |