Once received, cells were grown to 90% confluence in 75 cm2 tissue culture flasks and passaged according to methods described in their respective publications or as communicated by the creators of the cell lines. The culture media, serum, and substrate used for each cell line are indicated in
Establishing Chordoma Cell Line Collection
Once received, cells were grown to 90% confluence in 75 cm2 tissue culture flasks and passaged according to methods described in their respective publications or as communicated by the creators of the cell lines. The culture media, serum, and substrate used for each cell line are indicated in
Corresponding Organization :
Other organizations : Universität Ulm, Chordoma Foundation, National Cancer Institute, Duke University, Durham VA Medical Center
Protocol cited in 7 other protocols
Variable analysis
- Search terms used to identify chordoma cell line references ("chordoma cell line," "chordoma cell culture," and "chordoma AND in vitro")
- Solicitation of unpublished chordoma cell lines from attendees of the First (2007) and Second (2008) International Chordoma Workshops and through personal communication (JS) with researchers and clinicians
- Whether each resulting article described or reported use of a chordoma cell line
- Growth of received cell lines to 90% confluence in 75 cm^2 tissue culture flasks
- Culture media, serum, and substrate used for each cell line as indicated in Table 1
- Methods and media used for growing and passaging all other cell lines as recommended by the providers
- Primary human cultures consisting of middle passage MRC-5 (American Type Tissue Culture) derived from human embryonic lung or NHF1, a gift from M. Cordeiro-S`tone, derived from newborn foreskin
- Positive control: Not explicitly mentioned
- Negative control: Not explicitly mentioned
Annotations
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