Transfected Stable Cell Lines
Reliable | High-Performance | Wide Rage
Precision reporter, kinase, immune receptor, biosimilar, Cas9, and knockout stable cell lines for diverse applications.
Cat. No. : CSC-RR0254
Host Cell : A375 Size : >1x106 frozen cells/vial
| Cat. No. | CSC-RR0254 |
| Description | Luc/RFP Reporter Cell Line-A375 is engineered to stably co-express RFP and luciferase reporter genes. It is an ideal positive control for use in bioluminescence and fluorescence assays. In addition, A375 cells form tumors post implantation into immunocompromised mice. The in vivo growth of these tumors can be monitored using bioluminescent imaging or RFP fluorescent imaging. |
| Target Gene | Luciferase/RFP |
| Host Cell | A375 |
| Host Cell Species | Homo sapiens (Human) |
| Reporter Type | Fluorescent protein |
| Applications |
1. Gene expression studies 2. Protein localization 3. Drug screening and toxicology 4. Live cell imaging |
| Size | >1x106 frozen cells/vial |
| Stability | Validated for at least 10 passages |
| Quality Control | Negative for bacteria, yeast, fungi and mycoplasma. |
| Storage | Liquid nitrogen |
| Shipping | Dry ice |
| Revival | Rapidly thaw cells in a 37°C water bath. Transfer contents into a tube containing pre-warmed media. Centrifuge cells and seed into a 25 cm2 flask containing pre-warmed media. |
| Mycoplasma | Negative |
| Format | One frozen vial containing millions of cells |
| Storage | Liquid nitrogen |
| Safety Considerations |
The following safety precautions should be observed. 1. Use pipette aids to prevent ingestion and keep aerosols down to a minimum. 2. No eating, drinking or smoking while handling the stable line. 3. Wash hands after handling the stable line and before leaving the lab. 4. Decontaminate work surface with disinfectant or 70% ethanol before and after working with stable cells. 5. All waste should be considered hazardous. 6. Dispose of all liquid waste after each experiment and treat with bleach. |
| Ship | Dry ice |
https://pmc.ncbi.nlm.nih.gov/articles/PMC12801355/
The Researchers examined the in vivo interactions of self-assembled peptide amphiphile (PA) nanostructures with endogenous biomolecules to evaluate their potential for broad tumor targeting. Using a modular PA construct, SA‑E, they assessed cellular uptake, biodistribution, and therapeutic delivery across multiple human, murine, and patient-derived tumor models, including HCT‑116, A375, MCF7, 4T1, RG2, LL/2, and various transgenic and xenograft models. Cell lines were cultured under standard conditions with verified mycoplasma-free status, and select lines were transfected with lentivirus-expressed mCherry for membrane labeling. SA‑E facilitated tumor accumulation by dynamic assembly with circulating lipoproteins and interaction with cancer cell membranes, enabling imaging and chemotherapy delivery while minimizing off-target effects.
Figure 1. IVIS imaging demonstrates SA‑E accumulation across multiple solid tumor models, with strong concordance between ICG-labeled PA signal and tumor sites, including xenografts, patient-derived tumors, and transgenic lesions. (Xiang L, et al., 2026)
Creative Biogene–sourced human and murine cancer cell lines, along with reliable lentiviral tools for fluorescent labeling, support the development and evaluation of modular nanomaterials like SA‑E. These platforms enable mechanistic studies of tumor targeting, biodistribution, and therapeutic delivery in diverse preclinical models.
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