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-RO1118
Host Cell : SK-N-AS Size : >1x106 frozen cells/vial
| Cat. No. | CSC-RO1118 |
| Description | This cell line is engineered to stably overexpress human GFRAL in SKNAS cells. |
| Target Gene | GFRAL |
| Gene Species | Homo sapiens (Human) |
| Host Cell | SK-N-AS |
| Host Cell Species | Homo sapiens (Human) |
| Applications |
1. Gene expression studies 2. Signaling pathway research 3. Drug screening and toxicology 4. Disease research |
| 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 |
| Gene Name | GFRAL GDNF family receptor alpha like [ Homo sapiens ] |
| Gene Symbol | GFRAL |
| Synonyms | GRAL; UNQ9356; C6orf144; bA360D14.1 |
| Gene Description | GDNF family receptor alpha like |
| GeneID | 389400 |
| Uni ProtID | Q6UXV0 |
| mRNA Refseq | NM_207410.2 |
| Protein Refseq | NP_997293.2 |
| Chromosome Location | 6p12.1 |
The GFRAL gene (GDNF family receptor alpha like) is located on human chromosome 6p12.1 and encodes a glycosylphosphatidylinositol-anchored receptor protein that functions as the canonical receptor for growth differentiation factor 15 (GDF15). GFRAL is predominantly expressed in the brainstem and plays a critical role in energy homeostasis, body weight regulation, and appetite control. Upon GDF15 binding, GFRAL recruits the RET tyrosine kinase coreceptor and activates downstream signaling cascades including the MAPK and PI3K/AKT pathways, which mediate the anorectic and metabolic effects of GDF15. The Human GFRAL Stable Cell Line - SK-N-AS is generated by transfecting the human SK-N-AS neuroblastoma cell line with a full-length human GFRAL expression construct, followed by antibiotic selection to establish stable clones that constitutively express GFRAL on the cell surface. This cell line provides a reliable and reproducible in vitro model for investigating GFRAL-mediated signaling, GDF15 binding affinity, and receptor activation mechanisms.
This stable cell line serves as a valuable tool for a wide range of research applications. It is particularly useful for high-throughput screening of small molecule compounds, antibodies, or therapeutic peptides that modulate GFRAL activity, either as agonists or antagonists. Researchers can use this cell line to study the GDF15-GFRAL signaling axis in the context of metabolic disorders such as obesity, cachexia, and type 2 diabetes, where GFRAL has emerged as a promising drug target. The line can also be employed for ligand-receptor binding assays, internalization studies, and downstream signaling analysis, including phosphorylation of ERK, AKT, and other pathway effectors. Additionally, it supports the development and characterization of GFRAL-targeting biologics, including monoclonal antibodies and fusion proteins, aimed at treating conditions like cancer cachexia or metabolic syndrome.
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When studying the SK-N-AS cell line, I achieved the desired expression effect with only the lowest concentration used in the experiment. Good results were also achieved in subsequent in vivo experiments on tumor mice.
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