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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_03d0f52bb4069f8a19d70dcfb697c67a
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-37
filingDate 1999-07-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_69cece78cbb25bcef46aad8ad2b3d117
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cdb61ac20cc61bd6224fcc1d1ef0f5dd
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_619fe4aa098a0e9aed0d26ada8729f13
publicationDate 2000-11-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2000325096-A
titleOfInvention Protease measurement method
abstract PROBLEM TO BE SOLVED: To provide a method capable of accurately measuring protease activity in a biological sample and easily observing the morphology of a tissue or a cell. A method for measuring a protease, comprising the steps of (1) A step of bringing a biological sample containing a protease into contact with a thin film formed on the surface of a support containing a protease substrate and a hardener; (2) the thin film obtained in the above step is formed of red, orange, and yellow Staining with a dye selected from the group (for example, Ponceau 3R) and detecting a digestion mark formed on the thin film by the action of a protease; and, if necessary, (3) a step of, for example, staining a cell nucleus in the biological sample on the thin film with a dye (for example, hematoxylin) of a different color from the dye used in step (2).
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-2107122-A1
priorityDate 1999-03-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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