62.
    发明专利
    未知

    公开(公告)号:DE10229407A1

    公开(公告)日:2004-01-15

    申请号:DE10229407

    申请日:2002-06-29

    Inventor: STORZ RAFAEL

    Abstract: The present invention concerns a method for setting the system parameters of a scanning microscope, preferably a confocal scanning microscope, acquisition of an image of the specimen performed with the scanning microscope being controlled by a control computer. After an image of the specimen is acquired at least one image quality feature is inputted by a user and is converted by the control computer into at least one system parameter of the scanning microscope.

    63.
    发明专利
    未知

    公开(公告)号:DE10225838A1

    公开(公告)日:2003-12-24

    申请号:DE10225838

    申请日:2002-06-11

    Abstract: In a method for scanning microscopy an illuminating light beam that contains at least first light of a first wavelength and second light of a second wavelength, is coded. The coded illuminating light beam is directed onto a specimen and detection light proceeding from the specimen is decoded.

    METHOD OF ILLUMINATING AN OBJECT WITH LASER LIGHT

    公开(公告)号:GB2368743B

    公开(公告)日:2003-03-26

    申请号:GB0120663

    申请日:2001-08-24

    Abstract: A method for illuminating an object with light (2) from a laser light source (3), preferably in a confocal scanning microscope (1). With the method according to the invention, it is possible to reduce the coherence length of the laser light, so that disruptive interference phenomena can be substantially eliminated. Should interference phenomena nevertheless be formed, these are to be influenced in such a way that they have no effect on the detection. The method according to the invention is characterized in that the phase angle of the light field is varied by a modulator in such a way that interference phenomena do not occur in the optical beam path, or occur only to an undetectable extent, within a predeterminable time interval.

    Method for reducing interference by decreasing laser coherence in a confocal scanning microscope.

    公开(公告)号:GB2368743A

    公开(公告)日:2002-05-08

    申请号:GB0120663

    申请日:2001-08-24

    Abstract: A method for illuminating an object with light 2 from a laser light source 3, preferably in a confocal scanning microscope 1. With the method according to the invention, it is possible to reduce the coherence length of the laser light, so that disruptive interference phenomena can be substantially eliminated. Should interference phenomena be formed, these are to be influenced in such a way that they have no effect on the detection. The method is characterized in that the phase angle of the light field is varied by a modulation means 4 in such a way that interference phenomena do not occur in the optical beam path, or occur only to an undetectable extent, within a predeterminable time interval. Modulation means 4 may comprise an electro optical modulation (EOM), mirror, lens or beam splitter. Alternatively, the modulation means 4 may modulate the laser directly by switching it on and off, changing laser intensity and so on.

    Verfahren zur Überlagerung optischer Informationen bei einem Scan-Mikroskop

    公开(公告)号:DE102004047519B4

    公开(公告)日:2021-08-12

    申请号:DE102004047519

    申请日:2004-09-28

    Abstract: Verfahren zur Überlagerung optischer Informationen bei einem Scan-Mikroskop, wobei mindestens eine CCD-Aufnahme A mit mindestens einer weiteren Bildinformation B überlagert wird, wobei eine Transformationsmatrix T bestimmt wird, welche die Überlagerung der optischen Informationen der mindestens einen CCD-Aufnahme A und der mindestens einen Bildinformation B ermöglicht, wobei die Transformationsmatrix T zur Berücksichtigung jeweils unabhängiger Einflussgrößen durch Multiplikation einzelner Matrizen gebildet ist, so dass T=T1*T2*..., und wobei mindestens eine Matrix T1, T2, ... nichtlineare Abweichungen aufgrund nicht perfekter Galvanometer-Bewegungen berücksichtigt.

    70.
    发明专利
    未知

    公开(公告)号:DE502004003515D1

    公开(公告)日:2007-05-31

    申请号:DE502004003515

    申请日:2004-07-21

    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.

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