CellsBin® Scout™

CellsBin® Scout™

Reveal the Biology of Rare Therapeutic Cells in Blood

Scout delivers longitudinal single-cell insights with unmatched sensitivity, preserved phenotype, and decision-grade visibility for rare therapeutic cells in blood.

ActivationExhaustionCytokine ProductionProliferationMemory StatusTraffickingFunctionalityViability
1 in 1,000,000Rare-cell detection sensitivity
30+Surface & intracellular markers
48hReport turnaround
2 mLBlood input required

The observational gap

Scout Closes the Observational Gap in Cell and Gene Therapy

As therapeutic cells become rarer, conventional methods lose them. Scout keeps detecting — down to roughly one cell in a million, with phenotype preserved.

  • Flow cytometry lacks the sensitivity to resolve rare populations.
  • dd-PCR / NGS can count, but provides no phenotype insight.
  • CB-Scout™ makes rare cells detectable, quantifiable, and phenotypically interpretable at one-in-a-million sensitivity or better.
Sensitivity comparison
1101001K10K100K1M10M11110110011,000110,0001100,00011,000,000Number of therapy cells detectedTherapy-cell concentration in bloodFlow Cytometrydd-PCRCB-Scout™CellsBin extends the visibility.Down to 1 cell in ~1,000,000

Phenotypic depth

Reveal Surface and Intracellular Phenotypes at Single-Cell Level

Scout™ preserves phenotypic depth at the single-cell level, enabling drug developers and clinicians to profile both surface and intracellular markers from rare therapeutic cells in blood. This adds functional insight beyond simple detection and helps characterize state, identity, and biology over time.

CARCD27PD-1LAG-3CD62LCCR7TIM-3Granzyme BIFN-γIL-2CD45RACell-SurfaceMarkersIntracellularMarkers

Applications

One Observational Layer Across Cell Therapy Modalities

Scout supports diverse therapeutic formats with rich, single-cell phenotypic readouts — whatever the engineering approach, source, or delivery.

  • Engineered Immune Cell Therapies

    • CAR-T Cell Therapy
    • TCR-T Cell Therapy
    • CAR-Treg
    • CAR-NK / NK Cell Therapy
    • FasT Cell Therapy
  • Adoptive Cell Therapies (ACT)

    • TIL Therapy
    • Donor Lymphocyte Infusion (DLI)
    • Tumor-Targeted Lymphocytes
  • Stem, Regenerative & Platelet Therapies

    • HSC / HSCT
    • Mesenchymal Stem Cell (MSC) Therapy
    • Progenitor Cell Therapy
    • Platelet-Based Therapies
  • In Vivo & Smart Cell Therapies

    • In Vivo CAR-T
    • In Vivo Gene-Edited HSC
    • Smart Cell Therapies
    • M Cell Therapies

Workflow

From Samples to Answers

A simple, end-to-end experience for insights from rare therapeutic cells.

  1. 01

    Panel selection

    Select cell-surface and intracellular markers — a customizable panel tailored to your program.

  2. 02

    Sample collection & shipping

    Collect your sample — blood, PBMC, CSF, or other specimen types — and ship to CellsBin.

  3. 03

    Scout reporting

    CellsBin processes samples and delivers standardized, decision-ready Scout reporting.

Decision-grade packages

Across the Development Journey

One integrated approach to de-risk cell-therapy programs from IND readiness through long-term follow-up.

  • 01

    Preclinical / IND-Enabling

    Mechanism-of-action evidence designed to support 21 CFR 312.20(a)(8) requirements and strengthen IND readiness.

  • 02

    FIH Dosing / Dose Escalation

    In vivo pharmacokinetic evidence that complements safety data and supports first-in-human dosing decisions.

  • 03

    Phase I/II Translation

    Translational evidence linking pharmacokinetics to patient response, persistence, and emerging toxicity signals.

  • 04

    Long-Term Monitoring

    Longitudinal monitoring correlating pharmacokinetics with durability of response and late-onset adverse effects.

Start With a Pilot.

A low-friction entry point for biopharma teams seeking feasibility, longitudinal monitoring, or early clinical support.

  1. 01

    Design the pilot

    Define endpoints, markers, sample plan, and monitoring window.

  2. 02

    Run samples

    Generate standardized reports with decision-ready outputs.

  3. 03

    Scale the program

    Extend into IND-enabling studies or early clinical monitoring.