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| Species | Human |
| Cat.No | ABC-KH040Y |
| Quality Control | All cells test negative for mycoplasma, bacteria, yeast, and fungi. |
| Product Category | Transfected Stable Cell Lines |
| Size/Quantity | 1 vial |
| Cell Type | Epithelial |
| Shipping Info | Dry Ice |
| Growth Conditions | 37 ℃, 5% CO2 |
| Source Organ | Skin |
| Disease | Epidermoid Cancer |
| Biosafety Level | 1 |
| Storage | Liquid Nitrogen |
| Product Type | Knockout Stable Cell Line |
| Host Cell | A-431 |
| Gene Info | B2M |
Human B2M Knockout A-431 Cell Line is generated from human epidermoid carcinoma A-431 cells through CRISPR/Cas9-mediated disruption of the Beta-2-Microglobulin (B2M) gene, an essential component of MHC class I molecules required for antigen presentation. This knockout model exhibits complete loss of surface MHC class I expression while maintaining A-431 cells’ characteristic epithelial morphology, making it particularly valuable for studying immune evasion mechanisms in cancer immunotherapy. The cell line serves as a critical tool for research involving NK cell-mediated cytotoxicity, T-cell recognition, and immune checkpoint resistance, with specific applications in developing universal CAR-T cell therapies. Maintained at low passage numbers (<P20) with genetic stability, the knockout efficiency is validated through multiplex analysis including genomic PCR, Sanger sequencing, and flow cytometry confirming absence of MHC class I surface expression. The cell line has undergone rigorous quality control and is certified free of contamination from HIV-1, HBV, HCV, Syphilis, mycoplasma, fungi, yeast, and bacteria.
The Human B2M Knockout A-431 Cell Line is a specialized model for studying MHC class I antigen presentation and immune evasion mechanisms. This engineered system enables investigation of β2-microglobulin’s role in tumor immunogenicity and T-cell recognition. Researchers utilize this knockout line to examine disrupted HLA complex assembly and enhanced immune escape potential in squamous cell carcinoma. The cell line provides a controlled platform for evaluating novel immunotherapies targeting alternative immune recognition pathways in MHC-deficient cancers.