Primary cell lines derived from clinical tumor samples have the characteristics of easy cultivation, stable passaging, and the ability to conduct functional studies. They also retain the initial DNA genetic information and pathological features of tumors well, especially for rare disease specimens with special pathogenic mechanisms and genetic backgrounds. The effective construction of primary cell lines can greatly promote preclinical disease mechanism research and drug discovery efficiency.
In vitro drug efficacy research is a critical step in preclinical candidate drug screening. Traditional cell models fail to faithfully mimic the human microenvironment, leading to low clinical translation rates. Leveraging a standardized cell functional study platform, Jennio Bio adopts cutting-edge technologies such as high-content screening and 3D cell culture to build a highly biomimetic in vitro efficacy evaluation system, which significantly shortens drug R&D cycles and lowers clinical failure risks.
Technology Platform
Infrastructure
Differentiated Advantages
Case 1: High-Throughput Screening of Antitumor Drugs
Case 2: Antibody Immune Effect Evaluation

Q: Do you support in vitro evaluation of immune checkpoint drugs (e.g., PD-1/PD-L1)?
A: Yes. We have established PD-L1 fluorescent reporter lines and immune co-culture models to detect antibody blocking effects and T cell activation.
Q: What is the culture cycle and success rate of organoids?
A: Standard cycle 4–6 weeks, success rate >85%, with imaging records of the culture process provided.
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