For research use only
| Cat No. | ABC-KH001Y |
| Product Type | Knockout Stable Cell Line |
| Cell Type | Monocyte |
| Species | Human |
| Host Cell | THP-1 |
| Source Organ | Peripheral Blood |
| Disease | Acute Monocytic Leukemia |
| Storage | Liquid Nitrogen |
B2M Knockout THP-1 Cell Line by AcceGen provides an MHC class I-deficient human monocyte model for immunotherapy and immune evasion mechanism studies.
B2M Knockout THP-1 Cell Line is derived from the human monocytic THP-1 cell line, which serves as the host cell, and was generated via CRISPR/Cas9-mediated gene editing to disrupt the Beta-2-microglobulin (B2M) gene. THP-1 cells are suspension-grown immune cells with round morphology, commonly used to study monocyte/macrophage functions, immune responses, and inflammatory pathways. This knockout cell line exhibits loss of B2M expression, a key component of MHC class I molecules, making it valuable for research in immune evasion, antigen presentation, and immunotherapy. The edited cells are maintained at low passage numbers (<P20) to ensure genetic stability, and knockout efficiency is validated at the gene or protein level through PCR, Sanger sequencing, or Western blot. The cells are rigorously tested to ensure they are free of contamination from HIV-1, HBV, HCV, Syphilis, mycoplasma, fungi, yeast, and bacteria.
| Species | Human |
| Cat.No | ABC-KH001Y |
| Product Category | Transfected Stable Cell Lines |
| Size/Quantity | 1 vial |
| Cell Type | Monocyte |
| Growth Mode | Suspension |
| Shipping Info | Dry Ice |
| Growth Conditions | 37 ℃, 5% CO2 |
| Source Organ | Peripheral Blood |
| Disease | Acute Monocytic Leukemia |
| Biosafety Level | 1 |
| Storage | Liquid Nitrogen |
| Product Type | Knockout Stable Cell Line |
| Host Cell | THP-1 |
| Gene Info | B2M |
| Quality Control | All cells test negative for mycoplasma, bacteria, yeast, and fungi. |
The B2M Knockout THP-1 Cell Line is a genetically engineered human monocytic model with complete β2-microglobulin (B2M) gene disruption, resulting in deficient MHC class I surface expression. This modification provides a powerful tool for investigating immune evasion mechanisms, NK cell-mediated cytotoxicity, and MHC-independent immune responses. The cell line retains THP-1’s differentiation capacity while enabling studies of tumor immunology and immunotherapy development. Its consistent B2M knockout phenotype makes it particularly valuable for CAR-NK cell therapy research and HLA-related immunological studies.