• Flow cytometry analysis of cells with a up to 40 different markers on the same cells
• DNA cell cycle analyses
• Analysis of flow cytometry data in FlowJo or NovoExpress
• Image analysis with a maximum of 10 different markers - excellent for translocation studies as well as verifying a staining pattern
• Analysis of images from ImageStream in IDEAS

• Sorting heterogeneous single cell populations into homogeneous populations for down-stream experiments
• Sorting of cells with a maximum of about 20 different markers
• Sorting and/or index sorting of cells into 6-well, 12-well, 24-well, 96-well, 384-well, and 1536-well plates
• Sorting of cells - up to 6 different populations simultaneously - into tubes (0.2 ml, 1.5 ml, 5 ml, 15 m or 50 ml)
• Sorting on slides or chamber slides
• Single cell sorting for cloning
• Enrichment of rare cell populations
• Sorting can be performed at 4^oC, 20^oC, or 37^oC

• Advice in choosing the best combination of fluorochromes and setting up protocols
• Proof reading the relevant Materials & Methods and Result sections for publication

As a service for all users of the FACS Core Facility, the facility has subscribed for a license of "Fluorofinder Academic Plus access", which is a very helpful Automated and Intelligent Panel Designer. 

If you register with your au e-mail (.au.dk) you will get free access to this tool. When you register as an Aarhus University user, the software knows our instruments and their configurations including the Agilent Novocytes, the ID7000 and the BigFoot.

Register or Log on to Fluorofinder here.

Othe useful spectrum viewers

BD Spectrum Viewer

Invitrogen Spectrum Viewer

BioLegend Spectrum viewer

ThermoFisher Spectrum viewer

Search tools for antibodies

Biocompare enables you to search over 3 million antibodies from hundreds of antibody suppliers quickly and easily. Searches can be based on several experimental variables such as target antigen, species reactivity, host, conjugate or application. Compare antibodies from different companies side by side to find the one that best suits your research needs. 

Antibody quality

ASCEND by BenchSci uses AI and machine learning to screen open and closed access publications and display published figures with no commercial bias.

Searches can be based on several experimental variables such as target antigen, clone, reactivity, application etc.

Peer reviewed panels

Optimized Multicolor Immunofluorescence Panel (OMIP). These panels have been validated and published, in the Cytometry part A journal, and are a useful resource for developing immunophenotyping panels for a variety of applications.

Equipped with 6 lasers and 57 detectors.

It can sort into plates of up to 1536 wells and 6 way sorting from 1,5 ml tubes to 50 ml tubes. This sorter is inside a GMO class II biosafety cabinet.

Equipped with 4 lasers and 14 detectors (12 fluorescence, two light scatter)

Up to four-way sorting as well as for sorting to plates and slides

Equipped with 5 lasers and 147 detectors

Licence to run the analyzer is given to users after instructions by the FACS Core staff

Equipped with 3 lasers and 15 detectors (13 fluorescence, two light scatter)

Licence to run the analyzer is given to users after instructions by the FACS Core staff

Two instruments, each equipped with 4 lasers and 27 detectors (25 fluorescence, two light scatter)

Licence to run the analyzer is given to users after instructions by the FACS Core staff

Imaging flow cytometer with 5 lasers and 3 image magnification possibilities.

In total 12 channels (10 fluorescence, 2 bright field)

Equipped with 2 lasers and 12 detectors (10 fluorescence,two light scatter)

Licence to run the analyzer is given to users with permission to work in Class II lab.

Equipped with 5 lasers and 53 detectors.

It can sort into plates of up to 1536 wells and 6 way sorting from 1,5 ml tubes to 50 ml tubes. This sorter is inside a GMO class II biosafety cabinet.

Equipped with 5 lasers and 30 detectors (28 fluorescence, two light scatter).

Licence to run the analyzer is given to users after instructions by the FACS Core staff.