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Cell Phenotyping Assay

ACROBiosystems offers a diverse range of flow cytometry analysis solutions, built on a rigorously validated platform to precisely identify cell composition and status. Our product includes a wide selection of flow cytometry antibodies labeled with various fluorochromes, as well as ready-to-use premixed kits, designed to meet your needs across different flow cytometers. These high-quality, high-efficiency tools empower your immunophenotyping analysis in applications such as preclinical drug development and immune monitoring in clinical trials.

For more fluorescent dye labeling or color customization options, please click Inquire.

Flexible selection of fluorescent antibodies

Rapid Detection in Just 15 Minutes

Testing Workflow Diagram

Key Advantages

Flexible Selection:Offers both antibodies and kits, allowing flexible selection of fluorescent antibodies to analyses different cells.

Lightning-Fast Result: Achieve reliable staining in just 15 minutes with our one-step mixed antibody cocktail

Effortless Operation: Simply mix, incubation, and detect with a flow cytometer.

Universal Compatibility: Suitable for flow cytometers with blue and red lasers and six-color detection channels.

High Throughput: Capable of analyzing up to 50 samples simultaneously.

High Specificity: Validated with Isotype Control, FMO Control, and Mock Cell Controls.

Optimal Sensitively: Specially selected antibody and dye combinations ensure precise detection.

Reliable data validation:Verified by real PBMC samples

Cost-Effective: Proprietary antibody and fluorochrome coupling technology.

Product List

Fluorescent Antibody

Premixed Panel

Antibody Labeling Kits

Product Performance

Antibody Performance Data

Flow cytometric analysis of Jurkat cells staining with APC-Labeled Monoclonal Anti-Human CD3 Antibody, Mouse IgG2a (Clone: OKT3) (Cat. No. CDE-AHFP1) at 1:50 dilution (2μL of the antibody stock solution corresponds to labeling of 1e6 cells in a final volume of 100 µL) , compared with isotype control antibody. APC signal was used to evaluate the binding activity (QC tested).

Flow cytometric analysis of Raji staining with PE-Labeled Monoclonal Anti-Human HLA-DR Antibody, Mouse IgG2a(L243) (Cat. No. FABm020-01) at 1:20 dilution (5 μL of the antibody stock solution corresponds to labeling of 1e6 cells in a final volume of 100 µL), compared with isotype control antibody. PE signal was used to evaluate the binding activity (QC tested).

Panel Performance Data

Proven reliability with real PBMC samples

Start by setting the CD45/SSC scatter plot to identify the CD45+ lymphocyte population (A). Within the CD45+ gate, use the CD3/SSC scatter plot to identify the CD3+ T cell population (B). Next, use the CD3/CD4 scatter plot to identify the CD3+CD4+ helper T cells (Th gate) (C), and the CD3/CD8 scatter plot to identify the CD3+CD8+ cytotoxic T cells (Tc gate) (D). For B cells, use the CD3/CD19 scatter plot to identify the CD3-CD19+ population (B gate) (E). Finally, set the CD3/CD16+CD56 scatter plot to assess the CD3-CD56+CD16+ NK cell population (F).

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