For research use only
| Cat No. | ABC-KH004Y |
| 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 |
CD36 Knockout THP-1 Cell Line by AcceGen provides a validated model for studying lipid metabolism, inflammation, and phagocytosis in macrophages.
CD36 Knockout THP-1 Cell Line is engineered from the human monocytic THP-1 cell line using CRISPR/Cas9 technology to disrupt the Cluster of Differentiation 36 (CD36) gene, a key scavenger receptor involved in fatty acid uptake, phagocytosis, and inflammatory responses. As suspension cells with round morphology, these knockout THP-1 cells exhibit impaired lipid metabolism and modified immune functions, making them particularly valuable for research on atherosclerosis, metabolic disorders, and infectious diseases. The cell line maintains stable growth at low passage numbers (<P20), with knockout efficiency verified through PCR, Sanger sequencing, or Western blot analysis. All cells undergo stringent quality control and are confirmed free of contamination from HIV-1, HBV, HCV, Syphilis, mycoplasma, fungi, yeast, and bacteria.
| Species | Human |
| Cat.No | ABC-KH004Y |
| 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 | CD36 |
| Quality Control | All cells test negative for mycoplasma, bacteria, yeast, and fungi. |
The CD36 Knockout THP-1 Cell Line is a genetically modified human monocyte model with targeted disruption of the CD36 gene, resulting in loss of this scavenger receptor function. This engineered cell line provides a valuable tool for studying lipid metabolism, foam cell formation, and innate immune responses in atherosclerosis research. The modified cells enable investigation of CD36-mediated signaling pathways and their role in phagocytosis, inflammatory responses, and metabolic disorders.