http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20060108531-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_3f32d61079f1f77fbd1a73d702b5d21c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_439c5fede591ff9766f231d55b2f19db
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N2333-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N2333-01
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-569
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filingDate 2006-04-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7c5e180b392e47c29e6b483b2012b360
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ec9a851529fc173ef15d1a1137bdc27a
publicationDate 2006-10-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-20060108531-A
titleOfInvention Unamplified Multiple Quantitative Detection Kit and Detection Method for Pathogenic Microorganisms
abstract The present invention relates to an amplification-free quantitative detection kit for pathogenic microorganisms using a hybridization reaction and an enzyme-linked immunosorbent assay (ELISA), and a method for quantitatively detecting pathogenic microorganisms using the same. Hybridization module with a fixed fishing probe, tag-labeled reporter probe, standard sample, hybridization buffer, washing solution, denaturing solution, The detection kit of the present invention comprising a neutralizing solution, an antibody dilution solution, an enzyme-linked anti-tag antibody and a substrate solution of the enzyme is used for the hybridization reaction and ELISA without purification or amplification of the genetic material. Combination enables quantitative detection of several types of pathogenic microorganisms, such as viruses, bacteria, and protozoa at once. It is very economical in terms of time and money as it can be used.
priorityDate 2006-04-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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