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Microscope Stand Information


Unless otherwise stated the microscope objective lenses require specimens to be mounted on a #1.5 glass coverslip (170 microns) or in a chamber/dish with a coverslip bottom of the same thickness.

Widefield Microscopes

Use a widefield microscope if your specimen is thin and relatively free of out-of focus blur or you don't need to optically section it for processing, analysis and visualisation in 3D.

Microscope Name

Upright or Inverted?

Objective Lenses

Fluorescence Colours

Techniques

Axioplan

Upright for slidesUp to 100x

Blue, Green, Red, Far-Red

Zeiss Axioplan 2 microscope with QImaging QClick camera for high sensitivity and high resolution fluorescence microscopy and differential interference contrast (DIC) of fixed specimens on slides

Axio Imager

Upright for slides

Up to 100x

Blue, Green, Red, Far-Red (Cyan and Yellow available on request)

Zeiss Axio Imager A1 microscope with QImaging Retiga EXi for high sensitivity and high resolution fluorescence microscopy and phase contrast of fixed specimens on slides

Axioskop 3

Upright for slides

Up to 100x

Blue, Green, Red

Zeiss Axioskop microscope with QImaging QICAM colour camera for moderate to high resolution fluorescence microscopy and imaging of histologically or histochemically stained specimens on slides. Motorised stage supports tiling and stitching of specimens.

Leica

Inverted for TC dishes

Long distance air lenses up to 40x

Blue, Green, Red

Leica DMIRB microscope with Hamamatsu Orca NRB camera. Good for moderate resolution fluorescence microscopy and phase contrast of fixed/live specimens on slides, or in dishes and plates with glass or plastic bottoms

Leica 2

Inverted for TC dishes

Long distance air lenses up to 40x

Blue, Green, Red

Leica DMIRB microscope with Leica DFC7000T colour camera for high resolution fluorescence microscopy and colour imaging of histologically or histochemically stained specimens on slides, or in dishes and plates with glass or plastic bottoms

Confocal Microscopes

Use a confocal microscope if your specimen in thick, has significant out-of-focus blur, or if you need to process, analyse or visualise it in 3D.

Microscope Name

Upright or Inverted?

Objective Lenses

Laser Lines

Techniques

Radiance

Upright for slides

Up to 40x oil (water dipping lenses available)

458, 488, 514, 543, 635

Bio-Rad Microscience Radiance 2100 with Nikon 800 stand and three high-sensitivity GaAsP detectors for 3D imaging of fixed specimens on slides. DIC. Live imaging of specimens in gasket sealed chambers or open dishes possible using a heated stage adapter and lens heater. Fluorescence recovery after photobleaching (FRAP).

SPE

Upright for slides

Up to 63x oil (water dipping lenses available)

405, 488, 532, 640

Leica TCS SPE with DM2500 stand for 3D imaging of fixed specimens on slides. Live imaging of specimens in dishes possible with water dipping lenses using Oko-lab stage adapter or Warner Instruments perfusion chamber. DIC (not dipping lenses). Spectral imaging.

SPE

Upright for slides

Up to 63x oil (water dipping lenses available)

405, 488, 532, 640

Leica TCS SPE with DM2500 stand for 3D imaging of fixed specimens on slides. Live imaging of specimens in dishes possible with water dipping lenses using Oko-lab stage adapter or Warner Instruments perfusion chamber. DIC (not dipping lenses). Spectral imaging.

SPE3

Inverted

10x air to 63x oil

405, 488, 561, 640

Leica TCS SPE version 2 with DMI4000 stand for 3D imaging of specimens on slides and in dishes. DIC. Spectral Imaging. Motorised stage for multi-position acquisition and tiling. Matrix Screener software for high content screening.

SP5

Inverted

10x air to 63x oil (63x glycerol available)

405, 457, 476, 488, 495, 561, 594, 633

Leica TCS SP5 with DMI6000B for 3D imaging of specimens on slides and live imaging of specimens in 35 mm dishes and Lab-Tek chambered coverslips using Pe-Con incubation equipment. Spectral imaging. DIC. Motorised stage for multi-position acquisition and tiling. FRAP wizard. Förster Resonance Energy Transfer with FRET wizard. Experiment design using Live Data Mode. Matrix Screener for high content screening.

Spinning Disc Confocal Microscopes

Microscope Name

Upright or Inverted?

Objective Lenses

Laser Lines

Techniques

Vox

Inverted

10x air to 100x oil (60x water immersion available)

405, 488, 561, 640

Imaging of live specimens in 35 mm dishes, Lab-Tek chambered coverslips and Ibidi uSlides using Solent Scientific cage type incubation chamber. DIC. Multi-point and stitching. FRAP.

3iInverted10x air to 100x oil (40x water immersion available)405, 440, 488, 514, 561, 640Imaging of live specimens in 35 mm dishes, Lab-Tek chambered coverslips and Ibidi uSlides using Oko-Lab cage type incubation chamber. DIC. Multi-point and stitching. FRAP.

Time-lapse inverted microscope systems

Microscope

Objective Lenses

Fluorescence Colours

Camera

Techniques

GFP1

10x to 40x air and LWD (oil lenses available)

Green and Red

Greyscale high sensitivity CCD

Optimally configured for 'screening' of multiple positions in multi-well plates and other vessels at low to moderate resolution and high sensitivity using phase contrast and fluorescence. Stage adapters support Nunc and Mat-Tek multi-well plates and 35 mm Mat-Tek dishes. If you need to use another vessel or adapter you must contact Andrew Vaughan

GFP2

10x to 40x air and LWD (oil lenses available)

Blue, Green and Red

Greyscale high sensitivity CCD

Optimally configured for 'screening' of multiple positions in multi-well plates and other vessels at low to moderate resolution and high sensitivity using phase contrast and fluorescence. Stage adapters support Nunc and Mat-Tek multi-well plates and 35 mm Mat-Tek dishes. If you need to use another vessel or adapter you must contact Andrew Vaughan

N-STORM (coming soon)

10x air to 100x oil TIRF lens

Blue, Green, Red and Far-Red

Greyscale ultra-high sensitivity EMCCD

Optimally configured for high resolution and high sensitivity fluorescence microscopy of living specimens in XYZT for deconvolution, TIRF and super-resolution using N-STORM and dSTORM.

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