For research use only
| Cat No. | ABC-KH011Y |
| Product Type | Knockout Stable Cell Line |
| Cell Type | Epithelial |
| Species | Human |
| Host Cell | 293T |
| Source Organ | Kidney |
| Disease | Normal |
| Storage | Liquid Nitrogen |
SIRT4 Knockout 293T Cell Line by AcceGen supports advanced mitochondrial metabolism research and sirtuin-mediated cellular stress response analysis.
SIRT4 Knockout 293T Cell Line is generated from human embryonic kidney 293T cells through CRISPR/Cas9-mediated disruption of the Sirtuin 4 (SIRT4) gene, a mitochondrial NAD⁺-dependent deacylase involved in energy homeostasis and metabolic regulation. This knockout model exhibits altered mitochondrial metabolism while maintaining the characteristic adherent growth, epithelial morphology, and high transfection efficiency of 293T cells. It serves as a valuable research tool for investigating mitochondrial function, lipid metabolism, glutamine regulation, insulin secretion, and cancer metabolism. The knockout efficiency is validated through genomic PCR, Sanger sequencing, and Western blot analysis. The cell line is maintained at low passage numbers (<P20) to ensure genetic stability and has been rigorously tested free of HIV-1, HBV, HCV, Syphilis, mycoplasma, fungi, yeast, and bacteria.
| Species | Human |
| Cat.No | ABC-KH011Y |
| Product Category | Transfected Stable Cell Lines |
| Size/Quantity | 1 vial |
| Cell Type | Epithelial |
| Growth Mode | Adherent |
| Shipping Info | Dry Ice |
| Growth Conditions | 37 ℃, 5% CO2 |
| Source Organ | Kidney |
| Disease | Normal |
| Biosafety Level | 1 |
| Storage | Liquid Nitrogen |
| Product Type | Knockout Stable Cell Line |
| Host Cell | 293T |
| Gene Info | SIRT4 |
| Quality Control | All cells test negative for mycoplasma, bacteria, yeast, and fungi. |
The SIRT4 Knockout 293T Cell Line provides a specialized platform for mitochondrial metabolism research. By eliminating SIRT4 expression, it enables mechanistic studies of energy regulation, apoptosis, glutamine metabolism, and lipid homeostasis. This system is particularly valuable for cancer metabolism, metabolic disorder models, and neurodegenerative disease research. It also supports drug screening and discovery of new therapeutic targets linked to mitochondrial dysfunction.