宁波泰斯拓生物

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NCI-H187 [H187]

货号 TS211319
中文名称 null
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产品名称: NCI-H187 H187
商品货号: TS211319
Organism: Homo sapiens, human
Tissue: lung; derived from metastatic site: pleural effusion
Cell Type: Retinoblastoma
Product Format: frozen
Morphology: epithelial
Culture Properties: suspension, multicell aggregates
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: carcinoma; classic small cell lung cancer
Age: 47 years
Gender: male
Ethnicity: Caucasian
Applications: These cells are useful for transfection studies.
Storage Conditions: liquid nitrogen vapor phase
Derivation:
This line was derived by A.F. Gazdar, H.K. Oie, J.D. Minna and associates from cells recovered from pleural effusion obtained from a patient prior to therapy.
Clinical Data:
Caucasian
male
47 years

Oncogene: c-kit +; N-myc +
Tumorigenic: Yes
Effects:
Yes, the cells produce tumors in athymic nude mice
Comments:

NCI-H187 expresses elevated levels of the 4 biochemical markers of SCLC: neuron-specific enolase, the brain isoenzyme of creatine kinase, L-dopa carboxylase and bombesin-like immunoreactivity.

Only trace amounts of the retinoblastoma susceptibility gene (RB) mRNA, were detected.xa0RB protein was not detected.xa0The cells express the c-kit gene as well as the N-myc gene.

N-myc is not amplified.

The cells are not able to synthesize the peptide neuromedin B (NMB) or the gastrin-releasing peptide (GRP).

They express easily detectable levels of p53 mRNA compared to levels found in normal lung.


Complete Growth Medium: The base medium for this cell line is ATCC-formulated RPMI-1640 Medium, ATCC 30-2001. To make the complete growth medium, add the following components to the base medium: fetal bovine serum (ATCC 30-2020) to a final concentration of 10%.
Subculturing:

Cultures can be maintained by addition of fresh medium or replacement of medium. Alternatively, cultures can be established by centrifugation of the suspension with subsequent resuspension in fresh medium. Add medium as the cell density increases.xa0

Medium Renewal: Add fresh medium every 2 to 3 days (depending on cell density).
Cryopreservation:
Freeze medium: Complete growth medium, 95%; DMSO, 5%
Storage temperature: liquid nitrogen vapor phase
Culture Conditions:
Temperature: 37°C
STR Profile:
Amelogenin: X
CSF1PO: 11
D13S317: 12
D16S539: 11
D5S818: 12
D7S820: 9,10
THO1: 9.3
TPOX: 8
vWA: 16,17
Name of Depositor: AF Gazdar, JD Minna
Deposited As: Homo sapiens
References:

Little CD, et al. Amplification and expression of the c-myc oncogene in human lung cancer cell lines. Nature 306: 194-196, 1983. PubMed: 6646201

Takahashi T, et al. p53: A frequent target for genetic abnormalities in lung cancer. Science 246: 491-494, 1989. PubMed: 2554494

Carney DN, et al. Establishment and identification of small cell lung cancer cell lines having classic and variant features. Cancer Res. 45: 2913-2923, 1985. PubMed: 2985257

Hensel CH, et al. Altered structure and expression of the human retinoblastoma susceptibility gene in small cell lung cancer. Cancer Res. 50: 3067-3072, 1990. PubMed: 2159370

Plummer H, et al. c-myc expression correlates with suppression of c-kit protooncogene expression in small cell lung cancer cell lines. Cancer Res. 53: 4337-4342, 1993. PubMed: 7689933

Kaye FJ, et al. A single amino acid substitution results in a retinoblastoma protein defective in phosphorylation and oncoprotein binding. Proc. Natl. Acad. Sci. USA 87: 6922-6926, 1990. PubMed: 2168563

Giaccone G, et al. Neuromedin B is present in lung cancer cell lines. Cancer Res. 52: 2732s-2736s, 1992. PubMed: 1563005

NCI-Navy Medical Oncology Branch Cell Line Supplement. J. Cell. Biochem. suppl. 24: 1996.