34.
    发明专利
    未知

    公开(公告)号:DE102004032952A1

    公开(公告)日:2006-01-26

    申请号:DE102004032952

    申请日:2004-07-07

    Abstract: Disclosed is a method for analyzing biological samples by means of a scanning microscope. According to said method, at least one screen dot is repeatedly and successively illuminated with a manipulating light beam and an exciting light beam. The interval between the time of illumination with the manipulating light beam and the time of illumination with the exciting light beam is modified, and the fluorescent light yield is measured in accordance with said interval.

    36.
    发明专利
    未知

    公开(公告)号:DE10335466B4

    公开(公告)日:2005-09-01

    申请号:DE10335466

    申请日:2003-08-02

    Abstract: The scanning microscope (1) has an incoupling apparatus (31) with which light (33) other than the light (17) proceeding from the sample (7) is coupled into the detection beam path and conveyed to the detector (21). A closure apparatus automatically closes off the incoupling apparatus from the outside, in largely light-tight fashion, when the light guide (37) guiding the other light to the incoupling apparatus is removed. An independent claim is also included for confocal scanning microscope.

    39.
    发明专利
    未知

    公开(公告)号:DE10132638A1

    公开(公告)日:2003-01-16

    申请号:DE10132638

    申请日:2001-07-05

    Abstract: A scanning microscope examines a specimen (31). An optical component (89) has a characteristic that depends on wavelengths. A device uses wavelengths to perform detection that picks up measurement values in two wavelength ranges each characterized by spectral width and position. An Independent claim is also included for a method for using wavelengths to detect light emitted from a specimen by means of a scanning microscope.

    40.
    发明专利
    未知

    公开(公告)号:DE10055176A1

    公开(公告)日:2002-05-23

    申请号:DE10055176

    申请日:2000-11-08

    Abstract: An arrangement for visual and quantitative three-dimensional examination of specimens, having a stereomicroscope (2). The stereomicroscope defines a first and a second observation beam path (4, 5), by way of which a specimen (6) to be examined can be visually observed. A confocal scanning device (1) is connected to the stereomicroscope (1) in such a way that a scanning beam path (3) defined by the confocal scanning device (1) scans the specimen (6) that is to be examined and in that context acquires data for a three-dimensional visual depiction of the specimen (6).

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