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-RR00703
Host Cell : PC-12 Size : >1x106 frozen cells/vial
| Cat. No. | CSC-RR00703 |
| Description | PC-12-Luc reporter cell line is engineered to stably express Luciferase reporter gene in PC-12 cell line. |
| Target Gene | Luciferase |
| Host Cell | PC-12 |
| Host Cell Species | Rattus norvegicus (Rat) |
| 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 |
| Target Gene | Luciferase |
PC-12 cells are derived from a rat adrenal pheochromocytoma and are widely used as a neuronal model system in neurobiological research. They exhibit neuroendocrine properties and have the ability to synthesize, store, and release catecholamines such as dopamine and norepinephrine. One of their key features is their capacity to differentiate into neuron-like cells in response to nerve growth factor (NGF), developing neurite outgrowth and acquiring functional characteristics similar to sympathetic neurons. The Luciferase Reporter Cell Line – PC-12 is generated from this parental line through stable integration of a luciferase reporter construct under the control of specific response elements or promoters. This modification enables real-time monitoring of transcriptional activity associated with defined signaling pathways while preserving the fundamental biological characteristics of the original PC-12 cells.
The Luciferase Reporter Cell Line – PC-12 is commonly applied in studies of intracellular signaling, neurotoxicity, and neuropharmacology. It is particularly useful for evaluating pathway activation such as cAMP/PKA, MAPK/ERK, and calcium-dependent signaling in response to pharmacological compounds or biological stimuli. The luciferase readout provides a sensitive and quantitative measure of gene expression changes, making the system suitable for high-throughput screening of drug candidates targeting neuronal function or neurodegenerative mechanisms. In addition, this model is frequently used to investigate receptor-mediated signaling, including GPCR activation and downstream transcriptional responses. Its reliability and reproducibility make it valuable for compound efficacy testing, toxicity assessment, and mechanistic studies in neuronal differentiation and survival pathways, supporting both basic research and early-stage drug discovery applications.
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The PC-12 Luciferase Reporter Cell Line has been an asset to our neuro-differentiation research. Even after inducing differentiation with NGF, the luciferase activity remained robust and reproducible. It is a reliable tool for monitoring cellular responses in real-time.
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