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filingDate 1992-03-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b5963731fdab3a115cf9acc1ac483886
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publicationDate 1993-09-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H05245000-A
titleOfInvention Specific detection method for Mycobacterium tuberculosis
abstract (57) [Summary] [Objective] To provide a specific, highly sensitive and rapid detection method for Mycobacterium tuberculosis. [Structure] A method for specific detection of a Mycobacterium tuberculosis complex, which comprises extracting from a sample suspected of containing the Mycobacterium tuberculosis complex 16S rR DNA sequence containing the NA gene was extracted, and 16S r A primer complementary to a sequence specific to the M. tuberculosis group in the RNA gene DNA base sequence, which is a combination of an oligonucleotide primer for a sense strand and an oligonucleotide primer for an antisense strand, and 4 kinds of deoxynucleoside triphosphates Acid and DNA A synthase is applied to the extracted DNA solution to amplify a DNA fragment having the nucleotide sequences of both primers at both ends, the amplified DNA fragment is treated with a restriction enzyme, and the DNA after the restriction enzyme treatment The presence of the Mycobacterium tuberculosis group is detected by subjecting the amplified fragment to electrophoresis, immobilizing it on a nucleic acid binding membrane, hybridizing a labeled probe complementary to a part of the DNA amplified fragment, and detecting the label of the labeled probe. And a primer and a probe used in the method.
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