To solve the problem that various methods are in use for detecting single or multiple nucleotide variations, and most methods depend on amplification of a target sequence prior to analysis, commonly by PCR, so that valuable information on the localization of allelic variants is lost.
A method includes cutting a target nucleic acid near or preferably at the site which hybridizes with the padlock probe, whereby the 3'-end of the cut target nucleic acid acts as a primer for rolling circle replication of the padlock probe. Also included is a method of assaying a polyepitopic target by the use of two affinity probes each carrying an oligonucleotide tag and of a padlock probe for rolling circle replication in association with the two affinity probes.
WO1997019193A2 | 1997-05-29 | |||
WO1998004745A1 | 1998-02-05 | |||
WO1998004746A1 | 1998-02-05 |
Toshio Shirane
Sadao Muramatsu
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