An introductory training and brief formal orientation is mandatory for all users before beginning use of the facility. Training is provided for use of the analyzers and microscopes. Cell sorters are ONLY run by core employees and all experiments must be discussed with and scheduled with a core facility employee in advance. We do not permit access to the instruments for users who were not trained directly by Core staff.
It is imperative that you plan your experiments carefully. The Core is always available to consult on protocols and procedures prior to implementation and we strongly recommend you to come to us before starting any new experiment so as to avoid any expensive mistakes. This includes confirming that the fluorescent labels and their combinations can be analyzed on the instrumentation we have available in the Core.
Any non-routine multicolor/multifluorochrome experiment (i.e. not familiar to you/you have not done before) you wish to do should HAVE A pilot experiment done beforehand. In our experience, although our instrumentation has eight and ten multicolor capability the antibody titering and instrument set-up and compensation for four plus fluorochromes is not trivial and may take several pilot runs to work out. It is imperative that you discuss any complex multicolor experiment with a core employee prior to planning and/or ordering supplies so as to avoid any problems or misunderstandings. This is even more important if you wish to utilize the Cell sorter multi-color capabilities. Good communication with the cell sorter operator is also essential for the success of your experiments.
Your first visit
We therefore recommend the following procedure. First you make an appointment with the core facility were we dicuss the overall goals of your work and how to customize your experiments. When you have prepared your test samples according to the recommendations made during the initial meeting with the core facility, we will introduce you to the instruments making a basic aquisition setup with your samples or beads. With this data we then will show you the possibilities of data analysis located at the core facility, thereby discussing any future recommandations for your experiments.
This does also mean that NO SAMPLES for CELL SORTING will be accepted and NO ACCESS to the analyzers will be given without prior consultation with a core employee.
It is preferable to have already a filled out registration form at hand UserRegistrationForm when you first visit us.
Flow cytometry core facilities are multi-user facilities where many different samples from various sources that may contain known or unknown human pathogens are investigated. The safety of facility personnel and user is of ultimate concern. Because many of the investigators visiting the Core work with mice as model organism, this biosafety questionary has to be answered if any known mouse pathogens or transforming agents are used in the experiment.
Information about the sample sources and potentially infectious agents is critical for effective biosafety measures. Consequently, this sample information form must be filled out completely and signed by the laboratory director who is requesting samples to be analysed or sorted in the flow cytometry core facility before projects are started. The same biosafety questionaire will be kept on file provided none of the information it contains has changed. (biosafety questionary .pdf download)
We remind you that we are not allowed to process material beyond biosafety level 1 (S1).
|Development||Core Facility Users:||All Other Users|
|Analysis||no charge||12 €/h (Canto)
15 €/h (Fortessa)
|Sorting||no charge||80 €/h||160 €/h|
Core Facility Partners significantly contribute to the structure of the Core Facility, the development of techniques and the increase in knowledge in the field of Cytometry and related Sciences for the benefit of joint scientific projects. Expenses of the project are included in peer-reviewed funding or related cooperative projects, like for example the SFB 704 initiative.
Core Facility Users are members of the University of Bonn or Associates and have to contribute to the running costs of the Core Facility by internal cost allocation. Beside the access to the instrumentation of the core facility, they are given priority for training, service and assistance in design and interpretation of experiments by the Core Facility members as compared to other users.
All other users are all other users
Any formal presentations or publications resulting from work performed in the Core should be acknowledged and a reprint should be provided. Some instruments have been purchased from grants or other sources which also deserve acknowledgement. The following statement is suggested: “We would like to acknowledge the assistance of the Flow Cytometry Core Facility at the Institute of Molecular Medicine, University of Bonn, supported in part by SFB 704.”
For any details on the organisation or the design of future projects please contact Andreas Dolf
Users can make an arrangement with the core facility so that they can prepare their samples in the work areas of the facility. Core employees are available for advice on sample preparation and some reagents are available for testing.
All data must be collected on the hard drive. Data can be transferred using the build in CD/DVD writer or a USB device. Users get automatically an account on the data server of the core facility for convenience. The Core is not responsible for lost data, so please make sure that you have saved your data properly. Data that are older than 3 month will be removed without warning.
Data analysis is available on work stations located at the Core. There are two MacOSX computer were you can use Flowjo software from TreeStar Corp. for analysis. Some other data analysis programs are installed on our computers, e.g. VENTURIONE from Applied Cytometry or ModFit from Verity Software House (for cell cycle analysis). For details ask the core staff.
All samples run on our equipment must be in 12 X 75mm polystyrene tubes only from Sarstedt. (Ordering number: 55.1579.002) In general, cell densities should be 1×106 to 5×106/ml for the Canto, 1×106 to 5×106/ml for the LSRII or FACSDiVa, and each tube should have a volume of 300 μl to 1 ml.
ALWAYS bring NEGATIVE AND POSITIVE CONTROLS. To make appropriate conclusions about your samples the proper controls are necessary. Negative controls: Cells only (No stain). Specificity controls: If an indirect antibody staining method is employed, it is important to include a control in which cells have been stained with only the secondary antibody. This will indicate if there is “non-specific staining” or Fc region binding from the secondary antibody. Compensation controls: In experiments which require simultaneous staining using two or more fluorochromes, it is necessary to prepare controls that have been stained with each dye separately. These single color controls are required for adjusting cross-over signals between dyes or detectors and are crucial for multicolor immunophenotyping. Single stain controls can be performed on compensation particles e.g. from BD or Invitrogen.
Samples which are suspected of having aggregates (cell clumps) must be filtered (this is for analysers and sorters). Fourty micron nylon mesh is available at the Core. Falcon brand cell strainers for 50ml conical tubes (Falcon #35 2340 – 40um and Falcon#35 2350 – 70um) and filter top caps found on Falcon brand polystyrene 12×75 mm tubes (Falcon #35 2235) can also be used. We also recommend samples should be kept on ice or chilled until ready to run on the machine.
PLEASE SHOW UP ON TIME. You should give at least 24 hours notice if you need to cancel an appointment. If you are late for an appointment and run into the next users appointment you must stop acquiring your samples and finish at a later time. In particular if you are going to be late for a sorting appointment more than one hour then it is your obligation to check to see if your sort can still be done because other sorts may be scheduled on the same day. If there are other sorts scheduled then they will have priority.
All users are responsible for daily maintenance of the machine. After use, every user should follow the FACSCanto and LSR Start-up and Shut-down Maintenance procedure. Users that do not follow the rules, for example running unfiltered cells that clump and clog the machine, leaving the machine on, not doing End-of-Run maintenance and making sure that the waste is emptied and the sheath tank is filled, etc. will be identified and excluded from using the instruments. These instruments are common equipment and have to be treated with respect so that we may operate them for a long time without incurring additional expense due to misuse.