For research use only
| Cat No. | ABC-X0119C |
| Product Type | Overexpression Stable Cell Lines |
| Cell Type | Epithelial-like |
| Species | Human |
| Host Cell | CT26 |
| Source Organ | Colon |
| Disease | Colorectal Carcinoma |
| Storage | Liquid Nitrogen |
The human CXCR5 overexpression cell line (CT26) provides a powerful platform for immuno-oncology research, aiding the exploration of the CXCR5 signaling.
Xpress™ Human CXCR5 over-expressing cell line (CT26) is a genetically engineered model derived from the CT26 murine colon carcinoma cell line, developed according to customer specifications. Human CXCR5 overexpression was achieved through stable integration of the exogenous human CXCR5 gene into CT26 host cells via optimized lentiviral transduction technology, ensuring high and consistent expression levels suitable for functional studies.
Target
CXCR5 (C-X-C Motif Chemokine Receptor 5) is a G protein-coupled receptor primarily expressed on B cells and a subset of T cells, including T follicular helper (Tfh) cells. It plays a pivotal role in guiding cell migration to B-cell follicles by interacting with its ligand, CXCL13. CXCR5 has emerged as a key target in immune modulation and tumor microenvironment research, particularly in understanding lymphoid tissue organization and tumor-infiltrating Lymphocyte. AcceGen provides tailored overexpression models to facilitate studies in immuno-oncology and therapeutic antibody development.
| Species | Human |
| Cat.No | ABC-X0119C |
| Product Category | Transfected Stable Cell Lines |
| Size/Quantity | 1 vial |
| Cell Type | Epithelial-like |
| Growth Mode | Adherent |
| Shipping Info | Dry Ice |
| Growth Conditions | 37 °C, 5% CO₂ |
| Source Organ | Colon |
| Disease | Colorectal Carcinoma |
| Biosafety Level | 1 |
| Storage | Liquid Nitrogen |
| Product Type | Overexpression Stable Cell Lines |
| Host Cell | CT26 |
| Quality Control | All cells test negative for mycoplasma, bacteria, yeast, and fungi. |
The Xpress™ Human CXCR5 over-expressing cell line (CT26) serves as a robust platform for studying CXCR5-mediated signaling pathways, tumor-immune interactions, and the role of chemokine receptors in cancer progression. It is particularly valuable for evaluating targeted therapies, dissecting Tfh cell recruitment mechanisms, and screening antibodies or small molecules that modulate CXCR5 function in preclinical research.