Specifications
Description | AXL is a tyrosine kinase receptor and is involved in pathways and in cellular functions such as growth, migration, or aggregation. Some studies suggests AXL may play a role in susceptibility to ZIKV infection. This control cell line may be used with AXL knockout cell lines, such as T6232 or T6233 for comparison studies. |
---|---|
SKU | T8264 |
Species | Human (H. sapiens) |
Tissue/Organ/Organ System | Skeletal |
Donor Gender | Female |
Donor Disease | Fibrosarcoma |
Growth Properties | Adherent |
Cell Morphology | Epithelial-like |
Population Doubling Time | 20-30 hours |
Applications | For Research Use Only |
Unit quantity | 1×106 cells / 1.0 ml |
Cell Type | Tumor Cells |
Propagation Requirements |
Use of PriCoatTM T25 Flasks (G299) or Applied Cell Extracellular Matrix (G422) is required for cell adhesion to the culture vessels. Grow cells in ECM-coated culture vessels unless otherwise specified in the Propagation Requirements below. The base medium for this cell line is Prigrow III medium available at abm, Cat. No. TM003. To make the complete growth medium, add the following components to the base medium: fetal bovine serum (TM999) to a final concentration of 5%, Penicillin/Streptomycin Solution (G255) to a final concentration of 1%, and HEPES to a final concentration of 10 mM. |
Preservation Protocol | 1. Freeze Medium: Complete growth medium with 20% FBS and 10% DMSO. 2. Storage Temperature: Liquid nitrogen vapour phase. |
QC | 1) STR profiling |
Disclaimer |
|
Depositor | Mayo |
There are no FAQs for this product yet!
3
- Hitora, T., Yamamoto, T., Akisue, T., Marui, T., Nakatani, T., Kawamoto, T., … & Kurosaka, M. (2005). Establishment and characterization of a KIT‐positive and stem cell factor‐producing cell line, KTHOS, derived from human osteosarcoma. Pathology international, 55(2), 41-47.
- Persaud, M., Martinez-Lopez, A., Buffone, C., Porcelli, S. A., & Diaz-Griffero, F. (2018). Infection by Zika viruses requires the transmembrane protein AXL, endocytosis and low pH. Virology, 518, 301–312. https://doi.org/10.1016/j.virol.2018.03.009