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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6834
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-689
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filingDate 1999-06-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2001-11-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e04b3d6efee94426dceb8c5142495904
publicationDate 2001-11-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-100309944-B1
titleOfInvention Development of In situ Hybridization to detect Mycoplasma hyopneumoniae in formalin-fixed paraffin-embedded tissues without bacterial isolation
abstract The present invention relates to a method for diagnosing epidemic pneumonia in swine using intracellular hybridization, and more specifically, a specific DNA probe of mycoplasma hyopneumoniae, a pathogen of swine enzootic pneumonia (SEP). The present invention relates to a method for diagnosing a pandemic pneumonia in a pig that diagnoses infection and distribution of pathogens quickly and without bacterial separation by using in situ hybridization. . Therefore, according to the present invention, the present invention was able to overcome the problem of the fluorescent antibody method using only frozen tissues because it uses the lung tissue fixed in formalin, and also can detect a gene specific to mycoplasma hyopneumoniae only. As a result, cross-reactions were able to overcome the problems of immunohistochemistry, which was somewhat less specific. In addition, it solved the problem of necessarily requiring fresh tissue while showing sensitivity as high as that of the gene-level method using the polymerase chain reaction, and also observed the cells infected with mycoplasma hyopneumoniae through the optical microscope. It can be quickly and easily diagnose the infection and distribution of the pathogen is effective.
priorityDate 1999-06-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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