Flow Cytometry Core

About

The Flow Cytometry Core provides investigators with a resource for quantitative studies of cells, extracellular vesicles, and single-cell gene transcriptome analyses. The Core offers sample acquisition and analysis, cell sorting, and consultation for experimental design, interpretation and troubleshooting.

Radioactive materials are prohibited.


Contacts

Kewal  Asosingh, PhD, SCYM(ASCP)

Kewal Asosingh, PhD, SCYM(ASCP)
Associate Staff
Scientific Director, Flow Cytometry Core
Location:NB2-28A
Phone:(216) 444-0891
asosink@ccf.org
Research Profile

Amy  Graham, MS, SCYM (ASCP)

Amy Graham, MS, SCYM (ASCP)
Principal Flow Cytometry Technologist
Location:NE5-215
Phone:(216) 445-3798
grahama@ccf.org

Jena  Korecky,  BS

Jena Korecky, BS
Flow Cytometry Technologist
Location:NE5-215
Phone:(216) 445-3798
koreckj@ccf.org

Eric  Schultz, BS

Eric Schultz, BS
Flow Cytometry Technologist
Location:NE5-215
Phone:(216) 445-3798
schulte2@ccf.org

Services

Capabilities:

  • Apogee A50 Micro used for enumeration and fluorescence of small particle applications.
  • Zetaview Nanoparticle Tracking Analyzer.
  • Becton-Dickinson LSRFortessa capable of 18 color and 20 parameter acquisition with 5 lasers (355nm, 407nm, 488nm, 561nm, and 641nm).
  • Becton-Dickinson High Throughput Sampler (HTS) capable of acquiring samples from 96-well or 384-well microtiter plates on the LSRFortessa.
  • Becton-Dickinson SORP FACSAria Fusion high performance with ACDU, fixed alignment gel-coupled cuvette cell sorter. The BD SORP FACSAria Fusion cell sorter consists of 355nm, 405nm, 488nm, 561nm, and 637nm lasers, providing 20 parameters.
  • Becton-Dickinson FACS Melody cell sorter (488nm, 561nm, and 640nm direct diode lasers, providing 10 parameters).
  • All cell sorters are housed in specialty type Class II biological safety cabinets designed to offer personnel, product, and environmental protection from potentially aerosolized biological hazards.
  • 10x Chromium Controller for single cell partitioning for transcriptome analysis.
  • Cytek Aurora spectral flow cytometer equipped with five lasers (355nm, 405nm, 488nm, 561nm and 640 nm excitation wavelengths), three scattering channels, can detect up to 64 fluorescence channels. Samples can easily be acquired from 96 well plate format or single tube mode.

The Core provides data analysis with the following software:

  • Histogram Software (Apogee Flow Systems)
  • Flow Jo (Becton Dickinson)
  • ModFit LT (Verity)

SpectroFlo, FACSDIVA and FACSChorus are for acquisition only.

Analysis workstations and software training are available for researchers.

Consultation:

All investigators are encouraged to meet with the Scientific Director of the Flow Cytometry Core to discuss their experiment prior to ordering antibodies and other reagents. This meeting is often useful in that many potential problems can be averted before critical resources are used. The Core can also provide written protocols for staining, fixation and data analysis methods. Core technologists are available for assistance with sample acquisition, analysis and presentation. Materials available for reference in the Flow Cytometry Core lab include two introductory tutorials available in iLab, several textbooks on the basics of flow cytometry and the current protocols in cytometry. In addition, the Core frequently organizes training seminars for various levels of expertise. A meeting with both Flow Cytometry and Genomics Core directors is mandatory for pilot 10x experiments.

Flow Cytometry Applications:

  • Free of charge guidance in sample preparation and panel design, and affordable prices for instrument training and data analysis.
  • Functional assays utilizing fluorescent probes such as quantification of mitochondrial organelle function, calcium influx and apoptosis, and quantification of expressible fluorescent proteins.
  • 45 color cell surface and/or intracellular (cytokine) immunophenotyping.
  • Measurements of soluble factors in biological fluids and cell culture supernatants using bead-based multiplex assays.
  • Sample preparation and single cell partitioning using the 10x Chromium Controller .
  • Four-way sterile electrostatic cell sorting of preclinical and clinical samples for functional studies.
  • Extracellular vesicle enumeration and characterization.

Data is acquired as FCS 3.1 using Histogram Software on the Apogee A50. Micro SpectroFlo® is used on the Cytek Aurora. BD FACSDIVA Software is used to acquire data on the Fortessa and Aria II. Data can be imported/exported as FCS 2.0, 3.0, or 3.1 when using FACSDIVA. FACSChorus can be used to acquire data on the FACSMelody. Data acquired via FACSChorus can be exported as FCS 3.1. List mode acquisition and storage of data allows for analysis and presentation using many different formats according to the needs of the investigator. Data files are permanently stored in personal folders on Lerner Research Institute servers, readily available to all Lerner Research Institute employees with proper logon accounts. FlowJo and ModFit software are provided for analysis. Investigators are encouraged to schedule a training session to learn analysis of flow data utilizing one of the available software packages.

Getting Started with the Flow Cytometry Core:

Please visit our iLab page to schedule services. Users can find introductory materials, best practices and protocols on our Links & Resources page.

Equipment









Frequently Asked Questions

  1. Can I sort unfixed human samples?
    Yes. A BioProtect III Walk-In Clean Air and Containment Cabinet houses the FACSAria II. The BioProtect III is a specialty type Class II biological safety enclosure designed to offer personnel, product, and environmental protection from potentially aerosolized biological hazards. When a sort has a biohazard potential, a biohazard form must be completed prior to each sort via iLab.

  2. Can I run fluorochrome X with fluorochrome Y?
    To determine the spectral overlap of varied fluorochromes visit BD Biosciences or FluoroFinder. Select fluorochromes from the list and compare their excitation and emission wavelengths to get an idea of compatibility. Fluorochromes whose emission peaks overlap completely may not be used together.

  3. How many cells do I need for each tube? What should the volume be?
    Analytical experiments, under ideal circumstances, one million cells per tube are standard. In many situations, few cells may be available for each of the controls and experimental samples. The minimum number of cells required is going to vary based on needs. For very simple experiments, tens of thousands of cells may be needed. Multicolor experiments that subset out small percentages of cells may require several million cells per tube in order to acquire appropriate numbers of the target populations. (ref: Cytometry A. 2008 May;73(5):384-5. Roederer, M. How many events is enough?) A minimum of 200ul volume in each sample tube is required.

  4. What controls do I need for my experiment?
    Instrument controls consist of samples needed to compensate/unmix the different fluorochromes and to choose starting baseline voltages if optimal PMT voltages are not used. To properly compensate/unmix for an experiment, an unstained control (cells with NO fluorochromes) and a single color control for each fluorochrome for that experiment are needed. The instrument is set up using these controls for compensation/spectral unmixing. These controls are mandatory. FMO controls are highly recommended to set gate boundaries correctly. A consultutation with the Core Director is highly recommended to determine application specific controls.

  5. Do I really need all these controls?
    Yes. At times, the Flow Cytometry Core is called upon to setup the instruments without these controls. In these circumstances it is the Core's policy to inform the investigator that the instrument is being set so the data looks a certain way based on expectations and experience. Results from these experiments are invalid and need to be repeated with the proper controls. Any conclusions drawn under these circumstances are highly suspect at best.

  6. Do I really need to run compensation controls everyday?
    Yes. Even though the instruments are QC'd on a daily basis to measure stability and to provide researchers with platforms for reproducible data, there are always small differences in the instruments and more so in experimental set-up each day. Under proper setup, small changes in instrument settings are noticed from day to day. When differences in your control samples compared with experimental samples are seen, it is important to be sure it's really due to design, and not due to some errant fluctuation or improper set-up. For the spectral analyzers, a library of single color references can be created and used for subsequent experiments.

  7. Which pressure/nozzle settings are right for my sort?
    The nozzle size depends on the size and characteristics of the cells. The nozzle size should be about four to five times that of the cells that are being sorted. For sorts targeting most lymphocytes, the 70um nozzle is used. For larger cells, the 100um nozzle is used. Increased pressure and the smaller orifice of the 70um nozzle exposes the cells to a slightly harsher environment, albeit briefly. Delicate cells require the 100um nozzle regardless of their size.

For biosafety information, please visit the International Society for the Advancement of Cytometry's website.

Grant Information

The Flow Cytometry Core provides investigators with a resource for quantitative studies of cells and extracellular vesicles, and single-cell gene transcriptome analyses.

The Core offers sample acquisition and analysis, cell sorting, and consultation for experimental design, interpretation and troubleshooting. The Core is equipped with a 5 laser Cytek Aurora spectral analyzer with a 96-Well Automatic Sampling System. A Becton-Dickinson LSRFortessa capable of 18 color and 20 parameter acquisition with 5 lasers and High Throughput Sampler (HTS) is available for simple panels. The Core also has an Apogee A50 Micro Flow Cytometer capable of 3 color and 5 parameter acquisition with one laser and a Zetaview nanoparticle tracking analyzer is available for extracellular vesicle studies.

Biosafety Level 2 (BSL2) Compliant: Additionally, the Flow Cytometry Core includes a biosafety level 2 (BSL2) compliant cell sorters housed in Baker SterilGARD biosafety hoods. This instrument is located in a separate 176 square foot laboratory with a BioProtect III Walk-In Clean Air and Containment Cabinet that houses the FACSFusion and offers personnel, product, and environmental protection from potentially aerosolized biological hazards. The Core also offers a BSL2 compliant Becton-Dickinson FACSMelody cell sorter, consisting of 3 lasers, providing 10 parameters and is housed in a Baker SterilGARD to provide personnel, product, and environmental protection from potentially aerosolized biological hazards located in a 1,300 square foot facility. Both sorters are equipped with an aerosol management system to evacuate aerosols from the sort chamber. Standard operating procedures were developed for performing flow cytometry of samples from COVID-19 patients based on recommendations from the International Society for Advancement of Cytometry (ISAC) and approved by the Cleveland Clinic Institutional Biosafety Committee.

Data is acquired as FCS 3.0 using BD FACSDiva Software on the LSRFortessa and Aria II, and as FCS 3.1 using BD FACSChorus Software. Data can be imported/exported as FCS 2.0 or 3.0 or 3.1 when using FACSDiva. List mode acquisition and storage of data allows for analysis and presentation in many different formats according to the needs of the investigator. Data files are permanently stored in personal folders on the LRI servers, readily available to all Lerner Research Institute employees with proper logon accounts. FlowJo, Apogee Histogram and ModFit software are provided for analysis.

A Chromium Controller 10x Genomics instrument is available for automated single cell preparations and single cell gene expression applications. Evaluation of the single cell sample preparation, cell sorting (if needed), GEM creation, thermal cycling and cDNA amplification are performed in the Flow Cytometry Core. Further amplification and clean-up of libraries and sequencing are performed in our Genomics Core. The 10x Chromium Controller was purchased by the Lerner Research Institute in October 2018. The Core has successfully processed more than 800 clinical and mouse model samples. The samples were from various tissues including peripheral blood, cell culture, xenografts and surgical specimens. We offer 24/7 services to accommodate fresh clinical samples.

Flow Cytometry Core

  • Flow Cytometry Main Lab:
    NE5-215
    216.445.3798
  • FACSAriaII Lab:
    NE3-224
    216.636.2808
  • Email:
    FlowCore_LRI@ccf.org
  • Address:
    9500 Euclid Ave, NE5-215 (building NE, floor 5, room 215)
    Cleveland, OH 44195
  • Getting Started

    View prices and request services through iLab. Register for an iLab account and visit the desired core’s page to get started.

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