
Analytical Assays For Endpoint Data Collection
Flow Cytometry Services
State-of-the-art high-complexity flow cytometry throughout all stages of drug development.
At Champions Oncology, we offer an extensive range of flow cytometry services tailored to support your research. From custom flow panel design to fit-for-purpose validation, we provide specialized assays that deliver deep insights into immune response and tumor interaction. By leveraging both conventional and spectral cytometry technology, we help streamline complex flow cytometry studies in oncology, immuno-oncology, and hematology applications.
Overview
Industry Leader in Complex Flow Cytometry Solutions
Champions offers full custom development of multi-parameter panels
Industry best timelines featuring expedited development and optimization to meet your milestones
Operational expertise with quality assurance and the highest regulatory compliance for preclinical research
Ideally positioned to provide meaningful insights for your preclinical studies

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Advanced Preclinical Flow Cytometry with Custom Panel Development
We provide our off-the-shelf panels or custom flow cytometry panel design. We can also transfer your in-house developed panels to be executed in our labs at Champions, saving you time and resources.
Champions has expertise in several sample types as well as experience working with different species, such as mice, rats, rabbits, non-human primate (NHP), and human samples.
Study Design
Where Flow Cytometry Fits in Your Study Design
| Study Type | Why Flow Cytometry Matters | What We Offer |
|---|---|---|
| AML in vivo models | Bone marrow engraftment and disease burden are best measured directly, since peripheral blood doesn't reliably reflect what's happening in the marrow. | Engraftment panels ranging from a basic screen to deeper immune characterization. |
| Ex vivo co-culture | Flow is typically the primary readout for cell killing, and can confirm target expression directly within the culture system. | Co-culture killing and target-expression panels. |
| Humanized models (CD34 / PBMC) | Flow serves two roles here: confirming successful humanization before dosing, and characterizing immune cell populations after treatment. | Humanized T-cell, myeloid, and NK panels, from basic phenotyping to deeper characterization. |
| ADC studies | Target expression and receptor occupancy, measured by flow, are central to understanding how an antibody-drug conjugate engages its target. | Target-engagement panels tailored to your ADC. |
| T-cell engager / bispecific / immuno-oncology studies | Flow serves two roles here: confirming successful humanization before dosing, and characterizing immune cell populations after treatment. | T-cell killing and co-culture panels. |
| Solid-tumor PDX studies (including radiolabeled studies) | In immunodeficient host models, flow focuses on tumor target expression rather than immune profiling, since these hosts lack a full immune system. | Custom-scoped panels, developed with our flow team around your specific target and study design. |
If your study touches one of these areas, our scientists can help you determine whether flow cytometry belongs on your protocol from the start.
Best in Class
Our Instrumentation
BD FacSymphony:
5-laser, 24-color conventional flow cytometer, suited to high-throughput immunophenotyping
Cytek Northern Lights:
3-laser, 30-color full-spectrum cytometer, for expanded panel designs beyond conventional cytometry's limits
Cytek Aurora:
5-laser, 40+ color full-spectrum cytometer, for the highest-complexity panels and deepest immune profiling
Throughput of up to 400 samples per day, tissue dependent


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Testimonials
“We are thoroughly impressed with Champions Oncology's flow cytometry services. Their experts have delivered clear, actionable results that have significantly accelerated our research progress.”
Directory of Oncology, Biotech Company
“Their custom analysis and high-quality results have greatly enhanced our ability to study complex cell populations and validate our therapeutic targets.”
Translational Medicine Scientist, Pharmaceutical Company
“We are thoroughly impressed with Champions Oncology's flow cytometry services. Their experts have delivered clear, actionable results that have significantly accelerated our research progress.”
Directory of Oncology, Biotech Company
Timeline
What you receive, and when
| Stage | What You Receive | Typical Timeline |
|---|---|---|
| Raw Data | Unmodified .fcs files, delivered as soon as acquisition is complete | Approximately 48 hours |
| Standard analysis | Gated populations, cytograms, and summary graphs | Approximately 3 weeks (recent studies have averaged closer to 2) |
| Expedited analysis | The same deliverables as standard analysis, on an accelerated timeline | Approximately 5 business days (expedite fee applies) |
| Formal report | A complete written report | Aligned with your study's other end-of-study reports |

Get started
Speak to an expert
Resources
Explore Our Resources
- CYTO 2026 Poster #P003: A High-Dimensional Spectral Flow Cytometry Panel Incorporating Open-Channel Design to Enable Comprehensive Profiling of Human Immune Cell Heterogeneity in Peripheral Blood and PBMCsPoster - June 2026
- CYTO 2026 Poster #P011: Development of Robust Evaluation of T Cell Subsets with T-Cell Activation In a 3D Tumor–PBMC Co-Culture Model Enables Reliable Phenotyping and Cytotoxicity AssessmentPoster - June 2026
- Flow Cytometry in the Clinic: Benefits, Challenges, & OpportunitiesWhite Paper
- Using Flow Cytometry as an In Vivo Study EndpointBlog - January, 2023
- Flow cytometry and receptor occupancy in immune-oncologyPublication - February 2021
FAQ
Frequently Asked Questions
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Sample Preparation: Cells are harvested, counted, and often labeled with fluorescently conjugated antibodies that target specific markers.
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Fixing: Cells are fixed with formaldehyde to preserve structure and keep markers intact.
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Permeabilization: Required prior to staining for detection of intracellular cytokines.
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Blocking: Block for Fc receptors to prevent background stain uptake; block cytokine secretion with Brefeldin A and/or Monensin when measuring intracellular cytokines.
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Staining: Prepared cells are incubated with chosen antibodies or dyes, alongside negative and positive controls.
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Data Acquisition: Stained cells pass through the flow cytometer; lasers excite fluorophores and detectors measure emitted light.
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Data Analysis: Data are processed with specialized software to identify cell populations, marker expression, and viability.