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  Institute of Cell and Molecular Science
Flow Cytometry Core Facility equipment, images used with permission by BD
  Flow Cytometry Core Facility
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Flow Cytometry user form

Requirements

Potential users are requested to complete a "Flow Cytometry User Form" see below. This contains questions relating to the proposed flow cytometry use and will enable the user to determine whether the proposed use is feasible, how long the usage will be and so cost.

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Sample preparation

For multicolour analysis there is a requirement for single labelled cells or FACSComp beads to be prepared. This will then allow automatic compensation to be performed on the instruments.

All samples for sorting must be filtered (70μm). Tissue culture medium containing serum and antibiotics should be provided for sort collection.

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Costing

The cost of usage will be based on the training required, consultation time, set up time, number of samples analysed and the number and duration of sorts. ICMS Staff and associated Institutes costs will be £25 per hour for analysis, £40 per hour for sorting. External Academic costs are £40 per hour for analysis, £60 per hour for sorting. Industrial costs are £60 per hour for analysis and £100 per hour for sorting.

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Data analysis

For post acquisition data analysis FlowJo is available. Personal copies may be obtained from http://flowjo.com. [new window]

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Training

It is important that all users of the flow cytometers are trained to use the instruments to a minimum standard.   In house training will be available.

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User form

Part I
1.Description of proposed experiment(s)
2.Reason for experiment(s)
3. How many samples will be studied?
4. How many tubes per sample will be analysed?
5. How many fluorochromes will be used and which?
6. How will compensation be performed?
 
Part II
1.What will be the size of the cells?
2. What will be the likely cell count in the samples?
3. How many cell types will be sorted simultaneously (up to 4)?
4. How will the different cell types be identified?
5. What will be the required number of sorted cells for each type?
6. Will an asceptic sort be required?
7. Will purity or yield be required?
 
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by Gary Warnes. © Queen Mary, University of London 2007
Institute of Cell and Molecular Science, The Blizard Building, Barts and The London School of Medicine and Dentistry, 4 Newark Street, London E1 2AT, UK Tel: +44 (0)20 7882 2483, Fax: +44 (0)20 7882 2200