Page Comparison

h1. Leica

{float:right}!Leica.jpg|border=1!{float}

*Location: MRC Building room 3.17*

This is a Leica DMIRB inverted research fluorescence microscope suitable for observing cells on slides or in glass-bottomed or plastic bottomed vessels using either phase contrast or fluorescence microscopy. The microscope has a Hamamatsu C4742-95 Orca greyscale camera suitable for acquiring images of fluorescent specimens but not suitable for imaging histologically or histochemically stained specimens.

The microscope has 20x and 40x long working distance objective lenses that have adjustable correction collars so the objectives can be corrected to focus through different thicknesses. For example, coverslips are usually only 170 microns thick but the growth surface of standard cell culture dishes is approximately 1 mm thick, so a correction collar would have to be set differently for specimens mounted on one or other of these surfaces.

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h3. Objective lenses

|| Magnification \\ || Immersion \\ || Designation \\ || [NA|Glossary#NA] \\ || Contrast Technique \\ || Coverslip Correction (mm) \\ || [WD|Glossary#WD] (mm) \\ ||
| 10x \\ | Air \\ | N Plan \\ | 0.25 \\ | Ph1 \\ | None \\ | 17.6 \\ |
| 20x \\ | Air \\ | N Plan LWD \\ | 0.4 \\ | Ph1 \\ | 0 - 2 \\ | 3.2 - 1.9 \\ |
| 40x \\ | Air \\ | N Plan LWD \\ | 0.55 \\ | Ph2 \\ | 0 - 2 \\ | 3.3 - 1.9 \\ |

The [*Long Working Distance (LWD) objectives*|Glossary#LWD] have optical correction collars that must be  adjusted for the varying thicknesses of plastic culture vessels, cover  slips and other surfaces. Generally the collars will be set correctly  for plastic tissue culture dishes, but if you find it difficult to  satisfactorily focus on your sample it may be because the correction  collar has been adjusted for a different material. [This|http://lightmicroscopy.lmcb.ucl.ac.uk/Leica/Leica_Info.html] document contains instructions for adjusting correction collars.

h3. Fluorescence filter sets

|| Filter Position \\ || Filter Set \\ || Excitation Filter \\ || Dichroic Mirror \\ || Emission Filter \\ || Fluorophores \\ ||
| 1 \\ | Leica A4 \\ | 360/40 \\ | 400 \\ | 470/40 \\ | DAPI, Hoechst \\ |
| 2 \\ | Leica GFP \\ | 470/40 \\ | 500 \\ | 525/50 \\ | FITC, GFP \\ |
| 3 \\ | Leica N2.1 \\ | 515 - 560 \\ | 580 \\ | LP 590 \\ | Cy3, TRITC \\ |
| 4 \\ | Blank \\ | N/A \\ | N/A \\ | N/A \\ | Transmitted Light \\ |

Leica's [filter set|http://www.leica-microsystems.com/products/light-microscopes/accessories/filtercubes-and-fluorochromes/] web page.

h3. Camera Calibrations

The magnification calibrations for images taken using the Hamamatsu Orca camera with 0.63X de-magnifying C-mount are as follows:

|| Magnification \\ || [Binning Factor|Glossary#binning] \\ || 100 pixels = \\ || 1 pixel = \\ ||
| 10x \\ | 1 \\ | 106.34 µm \\ | 1063.4 nm \\ |
| 20x \\ | 1 \\ | 53.17 µm \\ | 531.7 nm \\ |
| 40x \\ | 1 \\ | 26.59 µm \\ | 265.9 nm \\ |
| 10x \\ | 2 \\ | 212.68 µm \\ | 2126.8 nm \\ |
| 20x \\ | 2 \\ | 106.34 µm \\ | 1063.4 nm \\ |
| 40x \\ | 2 \\ | 53.17 µm \\ | 531.7 nm \\ |

h3. Further Information

* [Leica DMIRB microscope stand instructions|^DMIRB-Controls.pdf]
* [Openlab software controls for Orca camera|^Orca-Openlab-Video-Control.pdf]