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Why Choose Next Generation Flow™?


Accelerate your research with BD’s Next Generation Flow Solution—an ultrasensitive, standardized approach that enables precise analysis of millions of cells (up to 10⁻⁶). Designed to support minimal residual disease (MRD) and primary immunodeficiency research, this integrated solution empowers you to move from sample to insight.

 

End-to-End Standardization
 

Ensure consistency and reliability with:

  • EuroFlow™-approved protocols.
  • Ready-to-use panels validated by multicenter clinical research groups.1,2
  • Automated analysis and reporting powered by expert-developed databases.1, 2, 3
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  1. Accelerated time to insight

    Accelerated time to insight
    Get results within hours of sample receipt—minimizing time spent on validation and maximizing time for innovation.4,5

  2. Streamlined workflow efficiency

    Streamlined workflow efficiency
    Simplify your process with intuitive protocols, pre-validated panels, and automated tools that reduce manual effort and error.

  3. Unmatched analytical power

    Unmatched analytical power
    Perform comprehensive immunophenotyping, analyze complex cell populations, and compare results against reference ranges with confidence.

  4. Global expert support

    Global expert support
    BD’s technical specialists are here to help you implement and scale these solutions worldwide.

BD Cytognos Multiple Myeloma MRD

 

Plasma cell panel endorsed by the IMWG as the gold standard for multicolor flow cytometry MRD studies including research studies of samples obtained post-anti-CD38 therapy.

 
BD Cytognos™ Multiple Myeloma MRD
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BD Cytognos Primary Immunodeficiency Orientation Tube


Standardized panel for immune profiling in peripheral blood supported by age-matched reference ranges enables detection of ESID-defined lymphocyte subpopulations.

 
BD Cytognos™ Primary Immunodeficiency Orientation Tube
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BD CytognosB-Cell Precursor Acute Lymphoblastic Leukemia MRD


Panel for standardized detection of normal and aberrant B-cell precursors including research studies of samples obtained post-CD19-targeted therapies.

 
BD Cytognos™ B-Cell Precursor Acute Lymphoblastic Leukemia MRD
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Watch Our Next Generation Flow™ webinars

 

“Next Generation Flow™ Technology in Multiple Myeloma Clinical Trials” 


- Dr. Bruno Paiva, PhD

"Next Generation Flow™ for Earlier Detection of Primary Immunodeficiency: Impact of late diagnosis in adult patients”

 

- Dr. Fernando Solano, MD, PhD, and Dr. Nahir Moreno, MD

“Comprehensive Analysis using Next Generation Flow™ in Multiple Myeloma MRD”

 

- Dr. Juan Flores-Montero, MD, PhD

“TBNK vs. Next Generation Flow Primary Immunodeficiency Orientation Tube testing for the screening of inborn errors of immunity”

- Professor Martín Perez-Andrés, PhD

References

  1. Kalina T, et al. EuroFlow standardization of flow cytometer instrument settings and immunophenotyping protocols. Leukemia. 2012;26, 1986-2010. doi: 10.1038/leu.2012.122

  2. Theunissen P, Mejstrikova E, Sedek L, et al. Standardized flow cytometry for highly sensitive MRD measurements in B-cell acute lymphoblastic leukemia. Blood. 2017;129(3):347-357. Doi:10.1182/blood-2016-07-726307

  3. van Dongen JJ, van der Velden VH, Brüggemann M, Orfao A. Minimal residual disease diagnostics in acute lymphoblastic leukemia: need for sensitive, fast, and standardized technologies. Blood. 2015;125(26):3996-4009. Doi:10.1182/blood-2015-03-580027

  4. Flores-Montero J, et al. Next Generation Flow for highly sensitive and standardized detection of minimal residual disease in multiple myeloma. Leukemia. 2017;31(10):2094-2103. Doi:10.1038/leu.2017.29

  5. van der Burg M, et al. The EuroFlow PID Orientation Tube for flow cytometric diagnostic screening of Primary Immunodeficiencies of the lymphoid system. Front Immunol. 2019:10:246. Doi:10.3389/fimmu.2019.00246.

  6. Verbeek M, et al. Minimal residual disease assessment in B-cell precursor acute lymphoblastic leukemia by semi-automated identification of normal hematopoietic cells: a EuroFlow study. Cytometry B Clin Cytom. 2024 Jul;106(4):252-263. doi: 10.1002/cyto.b.22143.

  7. Kumar S, Paiva B, Anderson KC, et al. International Myeloma Working Group consensus criteria for response and minimal residual disease assessment in multiple myeloma. Lancet Oncol. 2016;17(8):e328-e346. Doi:10.1016/S1470-2045(16)30206-6.

  8. Selliah N, et al. Multiple Myeloma EuroFlow assay validation for Clinical Trials. Poster presented at: ICCS 2019; Atlanta, Georgia, US.

  9. Van Dongen JJM, van der Burg M, Kalina T, et al. EuroFlow-Based Flowcytometric Diagnostic Screening and Classification of Primary Immunodeficiencies of the Lymphoid System. Front Immunol. 2019;10:1271. Published 2019 Jun 13. Doi:10.3389/fimmu.2019.01271

  10. Verbeek M, et al. Minimal residual disease assessment following CD19-targeted therapy in B-cell precursor acute lymphoblastic leukemia using standardized 12-color flow cytometry: A EuroFlow study. HemaSphere. 2025;9:e70125. doi: 10.1002/hem3.70125

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