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-RO0863
Host Cell : HEK293T Size : >1x106 frozen cells/vial
| Cat. No. | CSC-RO0863 |
| Description | This cell line is engineered to stably overexpress mouse ICOSL. |
| Target Gene | Icosl |
| Gene Species | Mus musculus (Mouse) |
| Host Cell | HEK293T |
| Host Cell Species | Homo sapiens (Human) |
| Applications |
1. Studying the interactions between immune cells and cancer cells 2. Studying the mechanisms of resistance to immune checkpoint blockade 3. High-throughput screening 4. Drug target validation |
| 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. |
| Growth Properties | Cells are cultured as a monolayer at 37°C in a humidified atmosphere with 5% CO2. Split at 80-90% confluence, approximately 1:3-1:6. |
| 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 |
| Gene Name | Icosl icos ligand [ Mus musculus ] |
| Gene Symbol | Icosl |
| Synonyms | B7h; GI50; GL50; B7-H2; LICOS; B7RP-1; GL50-B; ICOS-L; Icoslg; Ly115l; AU044799; BG071784; mKIAA0653 |
| Gene Description | icos ligand |
| Gene ID | 50723 |
| Uni Prot ID | Q544C7 |
| m RNA Refseq | NM_015790.3 |
| Protein Refseq | NP_056605.1 |
| Chromosome Location | 10 C1; 10 |
| Function | protein binding; receptor binding; |
| Pathway | Adaptive Immune System, organism-specific biosystem; Cell adhesion molecules (CAMs), organism-specific biosystem; Cell adhesion molecules (CAMs), conserved biosystem; Costimulation by the CD28 family, organism-specific biosystem; Immune System, organism-specific biosystem; Intestinal immune network for IgA production, organism-specific biosystem; Intestinal immune network for IgA production, conserved biosystem; |
A: The Mouse Icosl Stable Cell Line - HEK293T is typically derived from HEK293T cells by stable transfection of the Icosl gene. Its stability is ensured through continuous culturing and monitoring of Icosl gene expression.
A: In studies of immune co-stimulatory signals, Mouse Icosl Stable Cell Line - HEK293T can simulate T cell activation by expressing Icosl, thereby allowing the investigation of the signaling mechanisms involved in T cell co-stimulation.
A: In tumor immunotherapy research, Mouse Icosl Stable Cell Line - HEK293T can be used to evaluate the efficacy of immunotherapeutic strategies, such as Icosl antibody treatment, and to study its role in enhancing T cell immune responses.
A: The activity of the ASIC3 channel is typically evaluated in Mouse Icosl Stable Cell Line - HEK293T through electrophysiological recordings of channel activity and calcium ion imaging, among other techniques. The effects of drugs can be assessed using these experiments.
A: Addressing potential cell toxicity or adaptation issues may require optimizing culture conditions, screening for appropriate culture media, and adding relevant cytokines to ensure the health and adaptability of the cells in research.
A: Innovative applications of Mouse Icosl Stable Cell Line - HEK293T in immune co-stimulation research include studying novel co-stimulatory molecules, exploring new mechanisms of immune therapy, and evaluating new drugs for immunotherapy.
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