The White Confocal
0 Preface
1 Microscopy - an introduction
1.1 Lenses
1.2 The microscope
1.2.1 The objective lens
1.2.2 The eyepiece 1.2.3 The compound microscope
1.3 Resolution and the limits
1.3.1 Abbes formula
1.3.2 Glowing spots
1.3.3 Full width half maximum
1.3.4 Which ist he truth?
1.4 Beyond the limit of resolution
2 Fluorescence
2.1 What is fluorescence
2.1.1 The fluorescence process
2.1.2 Color games
2.1.3 Life times
2.2 Microscopy by fluorescence
2.2.1 Power ratio of excitation and emission
2.2.2 Transmitted light and incident light
2.2.3 Illumination
2.2.4 Excitation filter
2.2.5 Incident light and beam splitter
2.2.6 Emission filter 2.3 Artificial colours
3 Confocal microscopy
3.1 The reason
3.2 The principle
3.2.1 Spot illumination
3.2.2 Spot detection 3.3 The scanned image
3.3.1 Recording
3.3.2 Scanning procedures
3.3.3 Slice thickness
3.3.4 The third dimension
3.4 Two photon microscopy
3.5 Elements of a confocal microscope
3.5.1 Light source
3.5.2 Excitation filter
3.5.3 Primary splitter
3.5.4 Beam scanner
3.5.5 Objective lens
3.5.6 Channel separation 3.5.7 Emission filter
3.5.8 Sensor
3.6 The "white" confocal microscope
4 Light sources
4.1 Laser
4.2 Laser types
4.3 White light laser
5 Acousto optical excitation filter
5.1 How works an acoustooptical tunable filter?
5.2 Multichannel dimmer for laser light
5.3 Spectral freedom: AOTF and white light laser
6 White beam splitting
6.1 Acoustooptical beam splitter
6.2 AOBS and white source
7 Split of the emissions
7.1 Prism
7.2 Grating
7.3 Continuous separation: the spectrum
8 Emission filtering
8.1 &nb
About the Author:
Dr. Rolf Theodor Borlinghaus, born 1956, study of biology in Konstanz and promotion to Dr. rer. nat. at the biophysical institute. From 1990 product manager for complex fluorescence microscopy and confocal microscopy with Carl Zeiss Oberkochen (later Jena). Since 1997 with Leica Lasertechnik Heidelberg, now Leica Microsystems Mannheim. Today responsible for technology transfer and training.
