BasicsCoursePhDprog-PeterEvennetApril2012
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| − | | 10:25|| | + | | 10:25||11:05||align="center"|Session 1<br>Theory||align="center" | PRINCIPLES OF LIGHT MICROSCOPY<br>Historical aspects<br>Very basic components and principles ( incl. Refraction-basics)||align="center" |PETER EVENNETT (JAN)||align="center"| Jan shortly showing airy pattern from hole in mirror at one of the teaching microsopes (+ screen) |
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| − | | style="background:mediumseagreen;"|''' | + | | style="background:mediumseagreen;"|'''11:05''' |
| − | | style="background:mediumseagreen;"|'''11: | + | | style="background:mediumseagreen;"|'''11:15''' |
|align="center" style="background:mediumseagreen;"|'''BREAK''' | |align="center" style="background:mediumseagreen;"|'''BREAK''' | ||
|align="center" style="background:mediumseagreen;"|'''BREAK'''||align="center" style="background:mediumseagreen;"| ||align="center" style="background:mediumseagreen;"| | |align="center" style="background:mediumseagreen;"|'''BREAK'''||align="center" style="background:mediumseagreen;"| ||align="center" style="background:mediumseagreen;"| | ||
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| − | | style="background:LemonChiffon;"| 11:15|| style="background:LemonChiffon;"| 11: | + | | style="background:LemonChiffon;"| 11:15|| style="background:LemonChiffon;"| 11:50 |
| − | |align="center" style="background:LemonChiffon;"|SESSION 1<br>Practice<br> SHORT (5min !!!) Rotation|| align="center" style="background:LemonChiffon;"|capillary in oil demo <br>Coin-in-cup demo<br>red and green laser through milky water with black background||align="center" style="background:LemonChiffon;"| | + | |align="center" style="background:LemonChiffon;"|SESSION 1<br>Practice<br> SHORT (5min !!!) Rotation|| align="center" style="background:LemonChiffon;"|capillary in oil demo <br>Coin-in-cup demo<br>red and green laser through milky water with black background||align="center" style="background:LemonChiffon;"|PETE<br>PETER<br>SILKE & JAN || align="center" style="background:LemonChiffon;" |*capillaries, oil <br> * coin-in-cup, water <br>*laser pointer, glass with "milky" water and black background |
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| − | | 11: | + | | 11:50||12:45||align="center"|SESSION 1 <br>Theory|| align="center" | Introduction to lenses (Lens demo fun)<br>Lens aberrations (see colour fringes of lighting image with simple lens)<br> Resolution, Numerical aperture <br>Magnification||align="center" |PETER EVENNETT || align="center" | little lenses |
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| − | |17:05||17:25||align="center"|SESSION 3<br>Theory||align="center" |Koehler Illumination <br> (Microscope alignment)||align="center" |PETER EVENNETT || | + | |17:05||17:25||align="center"|SESSION 3<br>Theory||align="center" |Koehler Illumination <br> Epi illumination <br> (Microscope alignment)||align="center" |PETER EVENNETT || |
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| − | | 10:00||10:45||align="center"|SESSION 1<br>Theory||align="center" | | + | |style="background:LemonChiffon;"| 10:00 |
| + | |style="background:LemonChiffon;"|10:45||align="center" style="background:LemonChiffon;"|SESSION 1 <br>Theory & Practice||align="center" style="background:LemonChiffon;"| Eyepieces<br>Depth of Field<br>Depth of Focus ||align="center" style="background:LemonChiffon;"|PETER EVENNETT <br>LMF TEAM || align="center" style="background:LemonChiffon;"| students microscopes with 10x/0.25 and 40x/0.65 objectives <br> Stereoscope with a "sample" | ||
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| style="background:mediumseagreen;"|'''11:00''' | | style="background:mediumseagreen;"|'''11:00''' | ||
|align="center" style="background:mediumseagreen;"|'''BREAK''' | |align="center" style="background:mediumseagreen;"|'''BREAK''' | ||
| − | |align="center" style="background:mediumseagreen;"|'''COFFEE BREAK'''|| | + | |align="center" style="background:mediumseagreen;"|'''COFFEE BREAK'''|| style="background:mediumseagreen;"|''' ''' ||align="center" style="background:mediumseagreen;" | |
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| 11:00||12:45||align="center"|Session 2 <br> Theory & DEMONSTRATION || align="center"|Diffraction and Diffraction slide fun <br> Diffraction string show <br> ABBE'S DIFFRACTION EXPERIMENT<br>Peter's Video (50min) ||align="center"|PETER EVENNETT || align="center" | Diffraction slides, torch, "dashed" string | | 11:00||12:45||align="center"|Session 2 <br> Theory & DEMONSTRATION || align="center"|Diffraction and Diffraction slide fun <br> Diffraction string show <br> ABBE'S DIFFRACTION EXPERIMENT<br>Peter's Video (50min) ||align="center"|PETER EVENNETT || align="center" | Diffraction slides, torch, "dashed" string | ||
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| − | | 13:45||14: | + | | 13:45||14:15||align="center"| SESSION 3<br>Demo and Theory || align="center"| Dan's diffraction setup demonstration ||align="center" |SILKE ||align="center" |Dan's ABBE Diffraction demo setup |
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| − | + | | 14:15||15:00||align="center"|SESSION 1<br>Theory||align="center" | Lens aberrations and corrections ||align="center" |PETER EVENNETT || | |
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| − | | style="background:mediumseagreen;"|'''15: | + | | 15:00||15:30||align="center"|SESSION 1<br>Theory||align="center" | Introduction to contrast ||align="center" |PETER EVENNETT || |
| − | | style="background:mediumseagreen;"|'''15: | + | |- |
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| + | | style="background:mediumseagreen;"|'''15:30''' | ||
| + | | style="background:mediumseagreen;"|'''15:45''' | ||
|align="center" style="background:mediumseagreen;"|'''BREAK''' | |align="center" style="background:mediumseagreen;"|'''BREAK''' | ||
|align="center" style="background:mediumseagreen;"|'''COFFEE BREAK'''|| style="background:mediumseagreen;"|''' ''' ||align="center" style="background:mediumseagreen;" | | |align="center" style="background:mediumseagreen;"|'''COFFEE BREAK'''|| style="background:mediumseagreen;"|''' ''' ||align="center" style="background:mediumseagreen;" | | ||
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| − | | 15: | + | | 15:45 || 16:05 ||align="center"|SESSION 4<br>Theory|| align="center"| Dark Field microscopy||align="center" |PETER EVENNETT || |
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| − | |style="background:LemonChiffon;"| | + | |style="background:LemonChiffon;"| 16:05 |
|style="background:LemonChiffon;"| 16:30 ||align="center" style="background:LemonChiffon;"|SESSION 4<br>Practice|| align="center" style="background:LemonChiffon;"|Dark Field microscopy||align="center" style="background:LemonChiffon;"|LMF TEAM || align="center" style="background:LemonChiffon;"| diatome slides | |style="background:LemonChiffon;"| 16:30 ||align="center" style="background:LemonChiffon;"|SESSION 4<br>Practice|| align="center" style="background:LemonChiffon;"|Dark Field microscopy||align="center" style="background:LemonChiffon;"|LMF TEAM || align="center" style="background:LemonChiffon;"| diatome slides | ||
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| 9:00||10:00||align="center"|Recap ||align="center" | day 2 ||align="center" |LMF TEAM || align="center" |Questions | | 9:00||10:00||align="center"|Recap ||align="center" | day 2 ||align="center" |LMF TEAM || align="center" |Questions | ||
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| − | | 10:00||10: | + | | 10:00||10:30||align="center"|SESSION 1<br>Theory||align="center" | Objective reading||align="center" |PETER EVENNETT <br>LMF TEAM || align="center" |objectives, eyepieces, polylux |
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| + | | style="background:mediumseagreen;"|'''10:30''' | ||
| style="background:mediumseagreen;"|'''10:45''' | | style="background:mediumseagreen;"|'''10:45''' | ||
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|align="center" style="background:mediumseagreen;"|'''BREAK''' | |align="center" style="background:mediumseagreen;"|'''BREAK''' | ||
|align="center" style="background:mediumseagreen;"|'''BREAK'''|| align="center" style="background:mediumseagreen;"|'''BREAK''' || align="center" style="background:mediumseagreen;" | | |align="center" style="background:mediumseagreen;"|'''BREAK'''|| align="center" style="background:mediumseagreen;"|'''BREAK''' || align="center" style="background:mediumseagreen;" | | ||
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| − | |style="background:LemonChiffon;"| | + | |style="background:LemonChiffon;"| 10:45 |
| − | |style="background:LemonChiffon;"| | + | |style="background:LemonChiffon;"|11:45||align="center" style="background:LemonChiffon;"|SESSION 1<br>Practice<br>Group rotation||align="center" style="background:LemonChiffon;"| Cover glasses, sample mounting and Objective cleaning<br>Objective reading ||align="center" style="background:LemonChiffon;"|JAN<br>BRITTA, SILKE ||align="center" style="background:LemonChiffon;"| Coverglasses (High preciscion), different oils, slides, different cleaning reagents <br> at least 7 different, "interesting" objectives (for a group of 6-7) |
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| − | | | + | | 12:15||12:45||align="center"|SESSION 2<br>Theory||align="center" | Polarized light microscopy||align="center" |PETER EVENNETT || |
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| − | |align="center" | + | |
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| − | | | + | | style="background:mediumseagreen;"|'''12:45''' |
| + | | style="background:mediumseagreen;"|'''13:45''' | ||
| + | |align="center" style="background:mediumseagreen;"|'''BREAK''' | ||
| + | |align="center" style="background:mediumseagreen;"|'''LUNCH'''|| style="background:mediumseagreen;"|''' ''' || style="background:mediumseagreen;"|''' ''' | ||
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| − | | 16:00||17:10||align="center"|SESSION 4a<br>Theory & Demo|| align="center"|What is a pixel<br>Analog to Digital conversion<br>Nuyquist-Shannon||align="center" | | + | | 16:00||16:15||align="center"|Question round|| align="center"|Questions to Peter Evennett||align="center" |PETER EVENNETT <br>LMF TEAM || |
| + | |- | ||
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| + | | 16:15||17:10||align="center"|SESSION 4a<br>Theory & Demo|| align="center"|What is a pixel<br>Analog to Digital conversion<br>Nuyquist-Shannon<br>Quantitative Imaging||align="center" |MICHAEL || | ||
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| − | | 17:30||18:00||align="center"|SESSION 4b<br>Theory & Demo|| align="center"|Spatial Calibration and more||align="center" | | + | | 17:30||18:00||align="center"|SESSION 4b<br>Theory & Demo|| align="center"|Spatial Calibration and more||align="center" |MICHAEl || |
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| 9:00||10:00||align="center"|Recap ||align="center" | day 3 ||align="center" |LMF TEAM |||| | | 9:00||10:00||align="center"|Recap ||align="center" | day 3 ||align="center" |LMF TEAM |||| | ||
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| − | | 10:00||10:45||align="center"|SESSION 1<br>Theory||align="center" | Fundamental concepts of fluorescence ||align="center" | | + | | 10:00||10:45||align="center"|SESSION 1<br>Theory||align="center" | Fundamental concepts of fluorescence ||align="center" |MICHAEL||align="center" |- ||align="center" |- |
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| − | | 11:00||12:15||align="center"|SESSION 2<br>Theory & Practice||align="center" | Fluorescence Microscopy||align="center" |SILKE | + | | 11:00||12:15||align="center"|SESSION 2<br>Theory & Practice||align="center" | Fluorescence Microscopy||align="center" |SILKE||align="center" |• Light sources<br>• Lamp houses <br>• Spectra <br>• Filters <br> • Filter cubes <br> • Filter spectral charts of each microscope (laminated)||align="center" | • Spare lamp houses <br> • Lamps <br> • Ocean optics equipment <br> • Four (4) different Filter-sets (cubes), with the appropriate descriptions <br> • diagramms for drawing filter/fluorophore spectra |
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| − | | 14:00||15:45||align="center"|SESSION 3<br>Theory & Practice|| align="center"| | + | | 14:00||15:45||align="center"|SESSION 3<br>Theory & Practice|| align="center"|Detectors ||align="center" |BRITTA||align="center" | • CCD<br> • Cameras || align="center" |• CCD chip <br> *example cameras showing different chip sizes <br> • RGB Slider Spot Camera setup |
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| style="background:mediumseagreen;"|'''15:45''' | | style="background:mediumseagreen;"|'''15:45''' | ||
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|align="center" style="background:mediumseagreen;"|'''BREAK'''|| style="background:mediumseagreen;"|''' '''|| style="background:mediumseagreen;"|''' '''|| style="background:mediumseagreen;"|''' ''' | |align="center" style="background:mediumseagreen;"|'''BREAK'''|| style="background:mediumseagreen;"|''' '''|| style="background:mediumseagreen;"|''' '''|| style="background:mediumseagreen;"|''' ''' | ||
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| − | | 16:00||18:00||align="center"|SESSION 4<br>Practice|| align="center"|Imaging with CCD cameras using LMF systems ||align="center" |LMF TEAM ||align="center"|• Displaying <br>• Pixel size<br>• Look up table<br>• Binning<br>• Exposure time<br>• Saturation<br>• Signal to noise <br>• ROI<br>• Bit depth<br>• Auto map<br>• Auto contrast || align="center"|• Microscopes: <br> DVcore( | + | | 16:00||18:00||align="center"|SESSION 4<br>Practice|| align="center"|Imaging with CCD cameras using LMF systems ||align="center" |LMF TEAM ||align="center"|• Displaying <br>• Pixel size<br>• Look up table<br>• Binning<br>• Exposure time<br>• Saturation<br>• Signal to noise <br>• ROI<br>• Bit depth<br>• Auto map<br>• Auto contrast || align="center"|• Microscopes: <br> DVcore(Michael, 3 students)<br> N-Storm (Britta, 3 students)<br> L1 (Pete, 3 students)<br> self-built-syst (Jan, 3 students)) <br>• Fluorescence Sample slides (Kidney / Cells) |
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|align="center" style="background:mediumseagreen;"|'''BREAK'''||align="center" style="background:mediumseagreen;"|'''BREAK'''||align="center" style="background:mediumseagreen;"| ''note: break might have been too early? (usually in between the Optical sectioning talk)'' | |align="center" style="background:mediumseagreen;"|'''BREAK'''||align="center" style="background:mediumseagreen;"|'''BREAK'''||align="center" style="background:mediumseagreen;"| ''note: break might have been too early? (usually in between the Optical sectioning talk)'' | ||
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| − | |10:45||13:00||align="center"|SESSION 1<br>Theory & Demo||align="center" | Optical sectioning methods<br>Pros&Cons ||align="center" | | + | |10:45||13:00||align="center"|SESSION 1<br>Theory & Demo||align="center" | Optical sectioning methods<br>Pros&Cons ||align="center" |JAN ||align="center" |"confocal equipment": <br> laser pointer, mirror, broken scanning mirror <br> dual laser pointer (green and red) to demonstrate penetration of diff. wavelength |
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| − | | 14:00||15:00||align="center"|SESSION 2<br>Small Groups Discussion|| align="center"|What techniques might be good for me<br> (Own Projects) ||align="center" |LMF TEAM | + | | 14:00||15:00||align="center"|SESSION 2<br>Small Groups Discussion|| align="center"|What techniques might be good for me<br> (Own Projects) ||align="center" |LMF TEAM||align="center" | |
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Latest revision as of 10:21, 20 April 2012
Contents |
[edit] PhD Program: Basics of Light Microscopy - Peter Evennett / LMF - Course April 2012
[edit] Setup -Fri 13 April
Setup - all lmf staff move stuff to galleria Equipment needed
- Microscopes
- Optical bench
- Spinning disk gadget
- Polarazing sheets
- Diffraction Grids
- Fluorescent samples
- Fluorescent Beads (Prepare slides)
- First day Handout for students
- Light torches
- cameras and monitors
- Cleaning stations for each table
- condenser screwdrivers for each microsocpe
- oil/DIC objectives for each microscope (next to stand)
- 2 polarization filters for each microscope
[edit] DAY ONE (16th April)
| FROM | TO | ACTIVITY | TOPICS | Responsible person(s) | Materials needed |
| 9:00 | 09:30 | FINAL PREP | Test everything works | LMF | |
| 9:40 | 10:25 | INTRODUCTION | COURSE INTRO WHO is WHO? Round table |
LMF TEAM | White board and pen |
| 10:25 | 11:05 | Session 1 Theory |
PRINCIPLES OF LIGHT MICROSCOPY Historical aspects Very basic components and principles ( incl. Refraction-basics) |
PETER EVENNETT (JAN) | Jan shortly showing airy pattern from hole in mirror at one of the teaching microsopes (+ screen) |
| 11:05 | 11:15 | BREAK | BREAK | ||
| 11:15 | 11:50 | SESSION 1 Practice SHORT (5min !!!) Rotation |
capillary in oil demo Coin-in-cup demo red and green laser through milky water with black background |
PETE PETER SILKE & JAN |
*capillaries, oil * coin-in-cup, water *laser pointer, glass with "milky" water and black background |
| 11:50 | 12:45 | SESSION 1 Theory |
Introduction to lenses (Lens demo fun) Lens aberrations (see colour fringes of lighting image with simple lens) Resolution, Numerical aperture Magnification |
PETER EVENNETT | little lenses |
| 12:45 | 13:45 | LUNCH | LUNCH | ||
| 13:45 | 14:45 | SESSION 1 Practice 15min (!!!) Rotation |
Milky Glass Block demo Show and discuss microscope parts (upright and inverted) NA measurements |
JAN BRITTA SILKE |
*milky glass block, teaching microscope, coloured filters for microscope, iris objective *slides with arrows, simple upright and inverted microscope *horizontal protractor on stand, objective holder, 2 air objective with different (!) NAs (and maybe an iris objective), calculator, pencils, rubber |
| 14:45 | 15:30 | SESSION 2 Theory |
Microscope illumination Conjugate planes |
PETER EVENNETT | |
| 15:30 | 15:45 | BREAK | BREAK | ||
| 15:50 | 17:05 | SESSION 2 Practice (30min Rotation) |
conjugate planes on Peters microscope conjugate planes on optical bench |
PETER EVENNETT JAN |
*Peters microscope setup *optical bench demonstrating a transmitted light microscope, incl. light source |
| 17:05 | 17:25 | SESSION 3 Theory |
Koehler Illumination Epi illumination (Microscope alignment) |
PETER EVENNETT | |
| 17:15 | 18:30 | SESSION 3 Practice |
Koehler illumination (Microscope alignment) |
LMF TEAM | students manual microscopes, screwdrivers, nice brightfield sample |
[edit] DAY TWO (17th April)
| FROM | TO | ACTIVITY | TOPICS | Responsible person(s) | Materials needed |
| 9:00 | 10:00 | Recap | day 1 | LMF TEAM | Questions |
| 10:00 | 10:45 | SESSION 1 Theory & Practice |
Eyepieces Depth of Field Depth of Focus |
PETER EVENNETT LMF TEAM |
students microscopes with 10x/0.25 and 40x/0.65 objectives Stereoscope with a "sample" |
| 10:45 | 11:00 | BREAK | COFFEE BREAK | ||
| 11:00 | 12:45 | Session 2 Theory & DEMONSTRATION |
Diffraction and Diffraction slide fun Diffraction string show ABBE'S DIFFRACTION EXPERIMENT Peter's Video (50min) |
PETER EVENNETT | Diffraction slides, torch, "dashed" string |
| 12:45 | 13:45 | BREAK | LUNCH | ||
| 13:45 | 14:15 | SESSION 3 Demo and Theory |
Dan's diffraction setup demonstration | SILKE | Dan's ABBE Diffraction demo setup |
| 14:15 | 15:00 | SESSION 1 Theory |
Lens aberrations and corrections | PETER EVENNETT | |
| 15:00 | 15:30 | SESSION 1 Theory |
Introduction to contrast | PETER EVENNETT | |
| 15:30 | 15:45 | BREAK | COFFEE BREAK | ||
| 15:45 | 16:05 | SESSION 4 Theory |
Dark Field microscopy | PETER EVENNETT | |
| 16:05 | 16:30 | SESSION 4 Practice |
Dark Field microscopy | LMF TEAM | diatome slides |
| 16:30 | 16:50 | SESSION 5 Theory |
Basics of Phase Contrast microscopy | PETER EVENNETT | |
| 16:50 | 17:30 | SESSION 5 Practice |
Phase Contrast microscopy | LMF TEAM | cheek cell samples |
| 17:30 | : | SESSION 5 Theory |
Details of Phase Contrast microscopy | PETER EVENNETT |
[edit] DAY THREE (18th April)
| FROM | TO | ACTIVITY | TOPICS | Responsible person(s) | Materials needed |
| 9:00 | 10:00 | Recap | day 2 | LMF TEAM | Questions |
| 10:00 | 10:30 | SESSION 1 Theory |
Objective reading | PETER EVENNETT LMF TEAM |
objectives, eyepieces, polylux |
| 10:30 | 10:45 | BREAK | BREAK | BREAK | |
| 10:45 | 11:45 | SESSION 1 Practice Group rotation |
Cover glasses, sample mounting and Objective cleaning Objective reading |
JAN BRITTA, SILKE |
Coverglasses (High preciscion), different oils, slides, different cleaning reagents at least 7 different, "interesting" objectives (for a group of 6-7) |
| 12:15 | 12:45 | SESSION 2 Theory |
Polarized light microscopy | PETER EVENNETT | |
| 12:45 | 13:45 | BREAK | LUNCH | ||
| 14:00 | 14:40 | SESSION 2 Practice |
Polarized light microscopy | LMF TEAM | Hair, stone samples, benzocain cristals, rulers, gummi bears, plastic dishes, ... |
| 14:40 | 15:05 | SESSION 3 Theory |
Differential Interference Contrast (DIC) | PETER EVENNETT | |
| 15:05 | 15:40 | SESSION 3 Practice |
Differential Interference Contrast (DIC) | LMF TEAM | cheek cell samples |
| 15:40 | 16:00 | BREAK | BREAK | BREAK | |
| 16:00 | 16:15 | Question round | Questions to Peter Evennett | PETER EVENNETT LMF TEAM |
|
| 16:15 | 17:10 | SESSION 4a Theory & Demo |
What is a pixel Analog to Digital conversion Nuyquist-Shannon Quantitative Imaging |
MICHAEL | |
| 17:10 | 17:30 | SESSION 3 Practice |
PIXELS | LMF TEAM | Sesame seeds, sunflower seeds, nudels, gumibears and a checker board |
| 17:30 | 18:00 | SESSION 4b Theory & Demo |
Spatial Calibration and more | MICHAEl |
[edit] DAY FOUR (19th April)
| FROM | TO | ACTIVITY | TOPICS | Responsible person(s) | DEMO Activities | Materials needed |
| 9:00 | 10:00 | Recap | day 3 | LMF TEAM | ||
| 10:00 | 10:45 | SESSION 1 Theory |
Fundamental concepts of fluorescence | MICHAEL | - | - |
| 10:45 | 11:00 | BREAK | BREAK | BREAK | BREAK | BREAK |
| 11:00 | 12:15 | SESSION 2 Theory & Practice |
Fluorescence Microscopy | SILKE | • Light sources • Lamp houses • Spectra • Filters • Filter cubes • Filter spectral charts of each microscope (laminated) |
• Spare lamp houses • Lamps • Ocean optics equipment • Four (4) different Filter-sets (cubes), with the appropriate descriptions • diagramms for drawing filter/fluorophore spectra |
| 12:15 | 13:00 | SESSION 2 Practice |
Fluorescence imaging at microscopes | LMF TEAM | - | • Fluorescent labeled samples |
| 13:00 | 14:00 | BREAK | LUNCH | LUNCH | LUNCH | LUNCH |
| 14:00 | 15:45 | SESSION 3 Theory & Practice |
Detectors | BRITTA | • CCD • Cameras |
• CCD chip *example cameras showing different chip sizes • RGB Slider Spot Camera setup |
| 15:45 | 16:00 | BREAK | BREAK | |||
| 16:00 | 18:00 | SESSION 4 Practice |
Imaging with CCD cameras using LMF systems | LMF TEAM | • Displaying • Pixel size • Look up table • Binning • Exposure time • Saturation • Signal to noise • ROI • Bit depth • Auto map • Auto contrast |
• Microscopes: DVcore(Michael, 3 students) N-Storm (Britta, 3 students) L1 (Pete, 3 students) self-built-syst (Jan, 3 students)) • Fluorescence Sample slides (Kidney / Cells) |
| 19:00 | open end | Dinner | with Peter | LMF TEAM |
[edit] DAY FIVE (20th April)
| FROM | TO | ACTIVITY | TOPICS | Responsible person(s) | Materials needed |
| 9:00 | 10:30 | Recap | day 4 | LMF TEAM | Question sheets (!) |
| 10:30 | 10:45 | BREAK | BREAK | BREAK | note: break might have been too early? (usually in between the Optical sectioning talk) |
| 10:45 | 13:00 | SESSION 1 Theory & Demo |
Optical sectioning methods Pros&Cons |
JAN | "confocal equipment": laser pointer, mirror, broken scanning mirror dual laser pointer (green and red) to demonstrate penetration of diff. wavelength |
| 13:00 | 14:00 | LUNCH | LUNCH | LUNCH | |
| 14:00 | 15:00 | SESSION 2 Small Groups Discussion |
What techniques might be good for me (Own Projects) |
LMF TEAM | |
| 15:00 | 15:15 | BREAK | BREAK | BREAK | |
| 15:15 | 16:00 | SESSION 3 | Course evaluation | LMF TEAM |
