The FACS facility is closed at the moment due to the Corona Pandemie.
Flow Cytometry Core Facility at the “Centre for Infection Medicine”
The FACS Core Facility (FCF) offers all scientists of the Freie Universität Berlin access to established and innovative methods of cell analyses and sorting according to their specific needs and interests.
- Analyses and sorting of cells from different species, organs and compartments
(e.g. mouse, human, pig, dog; lymphatic organs, gut, skin, blood, epithelia)
- Analyses and sorting of cell lines, infected cells, transfected cells/organisms
(e. g. lymphocytes, cell lines, transfected cells)
- Sorting of infectious material (S2); requests for the sorting of material potentially harmful to the staff may be rejected
Our service includes:
- Operator-based cell sorting
- Independent sample acquisition and analyses
Both devices are equipped with 3 lasers (405, 488 and 632nm) and operated with the DIVA software.
service fee / h
Analyser (Canto II)
Sorter (Aria III)
70 € (incl. operator)
Using the calendars:
- Top right (log in): register with your Zedat-account -> Choose the device in the drop-down menu -> Double click on the favoured day -> Fill in the questionnaire -> Safe entries
- If changes are necessary: log in, enter changes, safe entries
- To copy an entry: log in, chose ‘copy’ and change date/time, safe
- To delete an entry: log in, double click on the entry and ‘delete’. Please do so latest one day before your appointment.
Bookings can’t be changed/deleted on the booked day. The devices can’t be booked on weekends and Berlin holidays. Bookings have to be deleted at least 24 h in advance or a 2h booking fee will be charged.
Before sorting of samples the aims and conditions have to be clarified with the operator. In case of standard sort procedures (human or mouse samples, standard dyes) this can be done via E-mail/telephone. The estimate sorting time and adjust the sorter set-up, the operator needs information on cell type (size, origin, infectious material), cell numbers (total, target cells), used fluorochromes and subsequent cell use (in vitro cultures, mRNA isolation etc.).
Samples for cell sorting have to be prepared properly:
- cell suspensions have to be filtered before sorting (40µm cell strainers).
- The sample buffer has to be free of phenol red.
- Samples treated with prodium iodide or DAPI are not accepted for sorting.
- The operator has to be informed in case other potentially leaky dyes are present in the samples.
- Unstained negative controls and fluorescence minus one controls (FMOC, in case of extensive fluorochrome panels and dim signals of target cell markers) may be helpful for setting up the sorting strategy.
The FCF staff offers help in preparing sorting strategies and fluorochrome panels.
The data are best directly saved on the server of the respective institute. Alternatively, data may be saved on the server of the institute and then transferred to portable devices.
External storage media must not be used on the computers connected to the sorter/analyser!
Data have to be deleted directly after export from the computers connected to the sorter/analyser.
Data are not permanently stored by the FCF.