http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2005145907-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_32681f1832d227fe8df23d12a37f67a8
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K16-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-543
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K14-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N21-78
filingDate 2003-11-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_704733ed989c5b7069c04586c8acf4ea
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cfc485e2ec3feec9986b9b5636ef85d6
publicationDate 2005-06-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2005145907-A
titleOfInvention Antibody fragment structure and its immunocomplex and immunoassay using the immunocomplex
abstract PROBLEM TO BE SOLVED: To provide a novel antigen concentration measuring method having excellent sensitivity and reliability. SOLUTION: A VL region polypeptide 1 that specifically binds to one antigen and a VH region polypeptide 3 are combined with each other via a particle 2 to form a multivalent antibody fragment structure. A body is prepared, and these are mixed and used in a combination capable of binding to the antigen 4 to form an immune complex through multiple bonds by the antigen 4 and the antibody fragment structure regardless of the number of epitopes. In addition, by using particles with a particle size of 1 μm or less in this antibody fragment structure, monodispersion is formed in a buffer solution used for immunoassay, and it has good measurement sensitivity even in measurement using a homogeneous system. To do. [Selection] Figure 1
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2007254397-A
priorityDate 2003-11-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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