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招聘公众号
ACROBiosystems百普赛斯基于流式细胞术平台，经严格的方法学验证，提供多样的流式分析方案，精准识别细胞组成及状态。我们提供多种荧光染料标记的流式抗体和预混试剂盒，满足您在流式细胞仪上的各种需求，为您在临床前药物开发、临床试验免疫监测等研究提供高质量、高效率的免疫细胞分型分析工具！
如有更多荧光染料标记或配色需求，请点击 咨询。
检测流程示意图
选择灵活：有荧光抗体和试剂盒可选，可灵活选择荧光抗体或试剂盒分析不同细胞；
操作时间短：使用混合抗体组合一步染色，实验流程仅需15 min；
标准细胞确认：经标准细胞确认真实样本细胞比例准确度；
通量高：可一次性检测50个样本；
高特异性：Isotype Control、FMO Control及Mock细胞对照验证均无非特异性结合；
最优抗体组合和浓度：试剂盒包含最佳抗体和染料组合，大大提升多色荧光实验的灵敏度；
可靠的数据验证：经过PBMC真实样本验证；
成本可控：基于自主抗体原料和荧光素偶联工艺开发，产品性能和供货能力有保障。
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).
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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