Immune profiling and biomarker platforms to support pre-clinical research
WuXi Biology provides discovery and clinical biomarker services for immuno-oncology research. Our technology platform includes a CAP-certified pathology lab, a flow cytometry and molecular biology lab, and GCP compliance. Our team is composed of highly-trained immunologists, board-certified pathologists, and biomarker experts.
Flow Cytometry
- >20 channel flow cytometry analysis
- Cover >60 cell marker/biomarker
- Baseline TIL (tumor-infiltrating leukocytes) data from >30 models
- Service covered TIL analysis
- Checkpoint/co-stimulatory marker analysis
- in vitro/in vivo phospho-flow
- Function analysis of immune cells
- High dimensional data mining
Pathology/Multiplex IF
- FFPE preparation/IHC/IF to support pre-clinical pathology diagnosis for drug safety evaluation, efficacy evaluation, etc.
- Multiplex IF focusing on immune microenvironment analysis, including
- Immune cell infiltration analysis,
- Spatial-proximity analysis,
- Secretory protein source determination,
- Complex tissue structure determination,
- Evaluation of gene expression regulation
- Provide biomarker testing in clinical studies, including
- H&E and histology analysis,
- FFPE sample process and slide cutting,
- IHC/ICC,IF, EHC, TCT, FISH, DISH, RNAscope, multiplex-IF, etc.
Case study: Optimization of human tumor dissociation process to eliminate hTIM-3 and hLAG-3 degradations

NanoString-based gene expression profiling
- Gene expression profiling with up to 800 genes in one panel
- Enabling GEP in difficult samples like FFPE
- Panel covering hot genes/pathways/function in immunology/oncology
Single-cell RNA sequencing platform and bioinformatics services
One-stop service covering sample processing, library preparation, sequencing, and bioinformatics analysis. Enabling cell type identification and phenotyping, differential gene expression analysis, functional enrichment and cell-cell interaction.
Molecular platform
- Quantitative polymerase chain reaction (qPCR) to support efficacy and safety evaluation (e.g. target gene copy number variation in CAR-T cells, and replication competent lentivirus (RCL) level in CAR-T cells).
- cMET exon14 skipping and EGFR mutation testing.