產(chǎn)品名稱 | SW480-Luc2 |
---|---|
商品貨號 | B161384 |
Organism | Homo sapiens, human |
Tissue | colon |
Product Format | frozen 1.0 mL |
Morphology | epithelial-like |
Culture Properties | adherent |
Biosafety Level | 2
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 | Duke's type B, colorectal adenocarcinoma |
Age | 50 years |
Gender | male |
Ethnicity | Caucasian |
Applications | Excellent signal/background ratio and stable Luciferase expression make this cell line ideal for in vivo bioluminescence imaging of xenograft animal model to study human cancer and monitor activity of anti-cancer drug. It also can be used in cell-based assays for cancer research. |
Storage Conditions | liquid nitrogen vapor phase |
Comments | This luciferase expressing cell line was derived from parental line CCL-228 by transduction with lentiviral vector encoding firefly luciferase gene (luc2) under control of EF-1 alpha promoter. This cell line was established through single cell cloning, and the cells constitutively express high levels of enzymatically active luciferase protein, which can be detected via in vitro and in vivo bioluminescence assays. The cells should be maintained in blasticidin (8 μg/mL) containing medium in routine cell culture. It is recommended to remove blasticidin prior to and during the experiment procedure when the cells are injected into animals in vivo, or co-cultured with other cell types in vitro. |
Complete Growth Medium | The base medium for this cell line is ATCC-formulated Leibovitz's L-15 Medium (ATCC 30-2003). To make the complete growth medium, add the following components to the base medium:
Note: The L-15 medium formulation was devised for use in a free gas exchange with atmospheric air. A CO2 and air mixture is detrimental to cells when using this medium for cultivation. |
Subculturing | Volumes used in this protocol are for 75 cm2 flask; proportionally reduce or increase amount of dissociation medium for culture vessels of other sizes. Corning® T-75 flasks (catalog #430641) are recommended for subculturing this product.
Interval: Maintain cultures at a cell concentration between 2 X 104 and 8 X 105 cell/cm2.
Subcultivation Ratio: A subcultivation ratio of 1:2 to 1:8 is recommended
Medium Renewal: 2 to 3 times per week |
Cryopreservation | Complete growth medium supplemented with 5% (v/v) DMSO (ATCC 4-X) |
Culture Conditions | Atmosphere: air, 100%;
Temperature: 37°C |
Cells per Vial | ≥ 1.0 x 106 cells |
Volume | 1.0 mL |
STR Profile | Amelogenin: X
CSF1PO: 13,14
D13S317: 12
D16S539: 13
D5S818: 13
D7S820: 8
THO1: 8
TPOX: 11
vWA: 16 |
Sterility Tests | Bacteria and yeast: No growth Mycoplasma: No growth |
Viral Testing | Hepatitis B: None detected Cytomegalovirus: None detected Human immunodeficiency virus: None detected Epstein-Barr virus: None detected Human papillomavirus: None detected |
Functional Tests | Luciferase activity: signal to noise ≥ 1,000 RLUs In Vitro Luminesence: 300,000 photons/cell/sec, subject to imaging and culturing conditions |
Population Doubling Time | approximately 55 hours |
Name of Depositor | ATCC |
Year of Origin | 2018 |
References | Zinn KR, et al. Noninvasive bioluminescence imaging in small animals. ILARJ 49: 103-115, 2008. PubMed: 18172337 Dothager RS, et al. Advances in bioluminescence imaging of live animal models. Curr Opin Biotechnol 20: 45-53, 2009. PubMed: 19233638 Fogh J, et al. Absence of HeLa cell contamination in 169 cell lines derived from human tumors. J. Natl. Cancer Inst. 58: 209-214, 1977. PubMed: 833871 Goodfellow M, et al. One hundred and twenty-seven cultured human tumor cell lines producing tumors in nude mice. J. Natl. Cancer Inst. 59: 221-226, 1977. PubMed: 77210034 Rangan SR. A new human cell line (FaDu) from a hypopharyngeal carcinoma. Cancer 29: 117-121, 1972. PubMed: 4332311 Faust JB, Meeker TC. Amplification and expression of the bcl-1 gene in human solid tumor cell lines. Cancer Res. 52: 2460-2463, 1992. PubMed: 1568216 Giard DJ, et al. In vitro cultivation of human tumors: establishment of cell lines derived from a series of solid tumors. J. Natl. Cancer Inst. 51: 1417-1423, 1973. PubMed: 4357758 |
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