Permits and Restrictions |
View Permits |
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Organism | Mus musculus, mouse |
Tissue | intestine |
Cell Type | intestinal neuroendocrine tumor cells |
Product Format | frozen 1.0 mL |
Morphology | epithelial-like |
Culture Properties | adherent |
Biosafety Level |
1
Biosafety classification is based on U.S. Public Health Service Guidelines, it is the responsibility of the customer to ensure that their facilities comply with biosafety regulations for their own country. |
Disease | invasive small intestinal neuroendocrine carcinoma |
Age | 10 to 13 weeks |
Strain | C57B1/6J |
Applications |
This cell line may be a useful model for human neuroendocrine neoplasms of the gut, and useful tools for studying hormone secretin. |
Storage Conditions | liquid nitrogen vapor phase |
Derivation | The STC-1 cell line was derived from the intestinal tumors of RIP1Tag2/Rip2pyST1 double transgenic mice. |
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Cellular Products | secretin |
Comments | The STC-1 cell line was derived from the intestinal tumors of double transgenic mice. Transgenic mice harboring a hybrid gene linking the rat insulin promoter (RIP) to polyoma small T (PyST) antigen were mated with transgenic mice harboring rat insulin promoter (RIP) linked to SV40 early region (Tag) creating off-spring harboring both transgenes (double transgenics). These mice were found to have frequent intestinal tumors in addition to pancreatic Beta-cell tumors. Gene expression studies suggested that the intestinal and pancreatic tumors arose as separate entities. The STC-1cell line produces the hormone secretin. This cell line may be a useful model for human endocrine neoplasms of the gut. |
Complete Growth Medium | The base medium for this cell line is ATCC-formulated Dulbecco's Modified Eagle's Medium, Catalog No. 30-2002. To make the complete growth medium, add the following components to the base medium: fetal bovine serum to a final concentration of 10%. |
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Subculturing |
Cells must be subcultured when they reach ~70% confluence, or else they start to come off the flask into suspension.
Volumes used in this protocol are for 75 cm2 flasks; proportionally reduce or increase amount of dissociation medium for culture vessels of other sizes.
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Cryopreservation | Freeze medium: Complete growth medium supplemented with 10% (v/v) DMSOStorage temperature: liquid nitrogen vapor phase |
Culture Conditions | Temperature: 37°C Atmosphere: air, 95%; carbon dioxide (CO2), 5% |
Cells per Vial | 1.0 x 10^6 |
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Volume | 1.0 mL |
Name of Depositor | Douglas Hanahan, PhD Cold Spring Harbor Laboratory |
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Year of Origin | June 1990 |
References |
Rindi G, et al. Development of Neuroendocrine Tumors in the Gastrointestinal Tract of Transgenic Mice. Am J Pathol 136(6): 1349-1363, 1990. PubMed: 2162628 Grant SGN, et al. Early Invasiveness Characterizes Metastatic Carcinoid Tumors in Transgenic Mice. Cancer Res 51: 4917-4923, 1991. PubMed: 1654206 |
Permits |
These permits may be required for shipping this product to Australia:
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Basic Documentation | Product Sheet Certificate of Analysis SDS |
References |
Rindi G, et al. Development of Neuroendocrine Tumors in the Gastrointestinal Tract of Transgenic Mice. Am J Pathol 136(6): 1349-1363, 1990. PubMed: 2162628 Grant SGN, et al. Early Invasiveness Characterizes Metastatic Carcinoid Tumors in Transgenic Mice. Cancer Res 51: 4917-4923, 1991. PubMed: 1654206 |