Transfected Stable Cell Lines
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Precision reporter, kinase, immune receptor, biosimilar, Cas9, and knockout stable cell lines for diverse applications.
Cat. No. : CSC-RR0593
Host Cell : SU-DHL-1 Size : >1x106 frozen cells/vial
| Cat. No. | CSC-RR0593 |
| Description | This cell line is engineered to stably express GFP reporter gene in SU-DHL-1 cells. |
| Target Gene | GFP |
| Host Cell | SU-DHL-1 |
| 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 |
RL is a human non-Hodgkin lymphoma B cell line created in 1983 by Walter J. Urba and Dan L. Longo. Exposure of RL cells to phorbol esters that activate protein kinase C, such as PMA and PdBu, induces significant growth inhibition. RL cells are reported to be negative for the Epstein-Barr virus genome. Researchers have extensively utilized the RL cell line for in vitro experiments to study the efficacy of new chemotherapeutic agents and targeted therapies. In addition, the RL cell line was used to create the CDX (cell line derived xenograft) RL xenograft mouse model. The RL xenograft model has been used as a model to study non-Hodgkin lymphoma treatments (immunotherapy using antibody conjugates, etc.).
Luciferase Reporter Cell Line - RL is a rigorously developed and stable cell line that features the integration of a luciferase reporter gene into the RL cells. This cell line is an indispensable tool in a variety of research applications, particularly in the areas of gene expression analysis, signal transduction studies, and drug discovery. Luciferase is an enzyme derived from fireflies that catalyzes a bioluminescent reaction that produces light. When this enzyme is expressed in RL cells, researchers can quantitatively measure cellular processes through luminescence. The intensity of the emitted light is directly related to the level of luciferase expression, providing a highly sensitive and non-invasive method for monitoring biological activity in real time.
The SU-DHL-1 cell line engineered to express green fluorescent protein (GFP) is a powerful tool in various fields of biomedical research. Here are some of its major applications:
Cancer research: SU-DHL-1 is a human diffuse large B-cell lymphoma (DLBCL) cell line. The introduction of GFP enables real-time visualization and tracking of tumor cell proliferation, invasion, and development in vitro and in vivo. This is particularly useful for studying mechanisms of lymphoma progression and testing the efficacy of anticancer drugs.
Drug screening and development: Researchers can use the GFP-expressing SU-DHL-1 cell line to perform high-throughput screening of potential therapeutic compounds. The fluorescent tag can easily identify the effects of drugs on cell viability, growth, and apoptosis, thereby accelerating the drug discovery process.
Gene expression studies: GFP acts as a reporter gene, allowing scientists to monitor the activity of other genes of interest. This makes it possible to study gene regulation, signaling pathways, and gene modifications in lymphoma cells. It helps dissect molecular pathways implicated in cancer and helps identify new molecular targets for treatment.
In vivo imaging: Cells expressing GFP can be implanted into animal models and tumor growth and metastasis can be monitored in real time using fluorescence imaging techniques. This application is critical for understanding tumor biology in a physiological context and for preclinical evaluation of anticancer therapies.
Cell tracking and migration studies: The fluorescence of GFP allows for detailed studies of cell migration and localization. In the context of lymphoma, it allows researchers to track the movement of cancer cells within tissues and understand how they spread in vivo. This information is critical for developing strategies to prevent metastasis.
Protein interaction studies: GFP-tagged proteins can be used to study protein-protein interactions within SU-DHL-1 cells. This can help identify key proteins involved in the pathogenesis of lymphoma and potentially discover new therapeutic targets.
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When we purchased the GFP Reporter Cell Line - SU-DHL-1, the customer support was excellent. They provided a detailed protocol and responded quickly to our inquiries.
The cells are easy to culture, and the GFP expression remains stable over time. This greatly enhances our ability to observe and analyze cell behavior. Great product!
The GFP signal is bright and easy to detect, which allows us to perform high-throughput screening with high precision. This product has exceeded our expectations.
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