Robot microscope
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Confocal imaging in 24-, 48-, 96-, 384- or 1536-well plates
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Environmental control: temperature, CO2, humidity
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Objectives: 20x and 60x water immersion
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Three CCD cameras and settings (se below) to visualize DAPI, CFP, GFP, YFP, RFP
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Dispenser unit for addition of compounds to wells
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Laser based auto focus
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Script-based Image and Data analysis program that can run during the experiment
HeLa cells transiently expressing EGFP-ALG-2 (green) and localisation of ER cargo marker p58/ERGIC (red), counterstained with Hoechst to show the nuclei (blue). Jonas Marstrand La Cour, UCPH BIO, Cell & Developmental Biology
Laser lines |
Primary Dichroics (beam spitters) |
CCD1 |
CCD2 |
CCD3 |
405 nm |
405/488/561/640nm |
450/50 |
540/75 |
|
488 nm |
405/488/640 nm |
520/35 |
565/40 |
|
561 nm |
405/561/640 nm |
540/75 |
585/40 |
690/50 |
640 nm |
|
565/40 |
600/40 |
690/50 |
Details
Microscope
High-content screening spinning disc confocal microscope, Opera QEHS, PerkinElmer
Location
North Campus, August Krogh Building,
Universitetsparken 13, 6. floor, room 624.
Typical applications
Live cell imaging, library screening, FRET
Consultation
Nynne Meyn Christensen
Michael Lisby
Training and problem reporting
Booking
Online via PPM.