http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1980842-A1

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filingDate 2007-02-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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publicationDate 2008-10-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1980842-A1
titleOfInvention Circular dichroism fluorescent microscope
abstract According to a circular dichroism fluorescent microscope 100, it is possible to analyze, by using a small amount of a sample and directly in a living organism, a high-order structure of the sample such as a biomolecule, for example, protein and the like. The circular dichroism fluorescent microscope 100 includes a confocal section (115). In the circular dichroism fluorescent microscope 100, a circularly polarizing/modulating section (105) converts, into right and left circularly polarized lights, a light beam emitted from a light source (103). Thus obtained right and left circularly polarized light is focused on the sample so that the sample is irradiated with the right and left circularly polarized lights. Then, an optical lens (102) focuses fluorescence emitted from the sample. Further, a wavelength selecting section (107) transmits only fluorescence having a predetermined wavelength. Subsequently, the fluorescence having passed through the wavelength selecting section 107 is detected. Based on fluorescent intensity signals of the fluorescence thus detected, a difference between (i) an intensity of the fluorescence emitted from the sample at the time of irradiation with the use of the right circularly polarized light and (ii) an intensity of the fluorescence emitted from the sample at the time of irradiation with the use of the left circularly polarized light is calculated.
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