Abstract:
PROBLEM TO BE SOLVED: To provide a high-purity lumbrokinase-containing protein having high safety. SOLUTION: The lumbrokinase-containing protein is obtained in high purity by using an automatic chromatography apparatus. A medicine and a functional food free from adverse effect and having high safety are each obtained by including the high-purity lumbrokinase-containing protein. COPYRIGHT: (C)2007,JPO&INPIT
Abstract:
PROBLEM TO BE SOLVED: To provide a simple and inexpensive monoatomic chip, and to provide its preparation method. SOLUTION: The monoatomic chip is prepared by a step for preparing a metal chip 1, a step for washing the metal chip 1, a step for applying a small amount of a noble metal to the metal chip 1 by electroplating and a step for forming a pyramidal structure terminated by a small number of atoms to the apex of the metal chip 1. COPYRIGHT: (C)2006,JPO&NCIPI
Abstract:
PROBLEM TO BE SOLVED: To provide an enhancer derived from α-amylase gene of rice usable to increase a promoter activity in a transformed plant cell or a transformed plant, and transformed plant cell and a transformed plant including the enhancer. SOLUTION: Disclosed are a transcriptional enhancer derived from αAmy8 gene of rice, a promoter operatively connected with the enhancer and a recombinant nucleic acid operatively connected with the promoter and having a coding sequence encoding a transcript. Disclosed are also a stably transformed plant cell and transformed plant including the recombinant nucleic acid or a similar recombinant nucleic acid having a transcriptional enhancer derived from a plurality of αAmy3 genes of rice. COPYRIGHT: (C)2003,JPO
Abstract:
PROBLEM TO BE SOLVED: To provide a method for rapid identification and determination of effects of an antimicrobial agent. SOLUTION: This method for test comprises the following steps (a) to (d): (a) incubating a specimen of a microorganism in a culture medium containing an antimicrobial agent at a continuously diluted concentration in a short time and providing the different total numbers of microorganisms, (b) amplifying the total different numbers of microorganisms according to an in vitro microbial DNA replication, (c) adding a reporter molecule, specific for a double-stranded DNA (dsDNA) and capable of forming a complex therewith to the resultant DNA amplification products and (d) observing the presence or absence of a signal release from the reporter molecule-dsDNA complex.