Immortalized Mouse Cranial Suture Cells (iMSu) are immortalized through infection with non-replicating retrovirus carrying the loxP-flanked SV40 large T antigen. In vitro, the cells can be genetically manipulated for further research. Thus it is a reliable tool for research in mouse cranial suture biology and molecular signalling mechanism implicated in cranial sutures pathophysiology such as craniosynostosis.Immortalization Method: Serial passaging and infection with retrovirus carrying loxP-flanked SV40 large T antigen BioSafety Level: IISpecies: MouseSource Organ: CraniumGrowth Properties: AdherentMorphology: PolygonalPopulation Doubling: 21 hoursSeeding Density: 20,000 cells/cm²Markers: N/ADonor Age: N/ADonor Gender: N/ADonor Ethnicity: N/APropagation: The base medium for this cell line is Prigrow III medium available at abm (TM003). To make the completed growth medium, add the following components to the base medium: fetal bovine serum (TM999)* to final concentration of 10% and Penicillin/Streptomycin Solution (G255) to a final concentration of 1%. Carbon dioxide (CO2): 5%, Temperature: +37.0°C.* abm does not recommend to use heat-inactivated FBS for cell culture unless specified otherwise.Quality Control: N/AShipping Condition: Dry IceStorage Condition: liquid nitrogen or -180°C