宁波泰斯拓生物

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NCI-H358 [H-358, H358]

货号 TS211269
中文名称 null
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产品名称: NCI-H358 H-358, H358
商品货号: TS211269
Organism: Homo sapiens, human
Tissue: lung/bronchiole; derived from metastatic site: alveolus
Product Format: frozen
Morphology: epithelial
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: bronchioalveolar carcinoma; non-small cell lung cancer
Gender: male
Applications:
This line was derived by A.F. Gazdar, H.K. Oie, J.D. Minna and associates in 1981 from tumor tissue obtained from a patient prior to initiation of chemotherapy.
Ultrastructural studies demonstrated the presence of cytoplasmic structures characteristic of Clara cells.
Storage Conditions: liquid nitrogen vapor temperature
Images: TS211269 Cell Micrograph
Derivation:
This line was derived by A.F. Gazdar, H.K. Oie, J.D. Minna and associates in 1981 from tumor tissue obtained from a patient prior to initiation of chemotherapy.
Clinical Data:
male
Genes Expressed:
lung surfactant associated protein A (SP-A),The cells expressed protein and RNA of SP-A, the major lung surfactant associated protein.
Cellular Products:
lung surfactant associated protein A (SP-A)
Tumorigenic: Yes
Effects:
Yes, the cells produce tumors in athymic nude mice
Comments:
Ultrastructural studies demonstrated the presence of cytoplasmic structures characteristic of Clara cells.
The cells expressed protein and RNA of SP-A, the major lung surfactant associated protein.
SP-B and SP-C RNA was not expressed.
They have a reported colony forming efficiency of 0.83% in soft agarose.
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:

Remove medium, and rinse with 0.25% trypsin, 0.53 mM EDTA solution. Remove the solution and add an additional 1 to 2 mL of trypsin-EDTA solution. Allow the flask to sit at room temperature (or at 37°C) until the cells detach. Add fresh culture medium, aspirate and dispense into new culture flasks.

Subcultivation Ratio: A subcultivation ratio of 1:3 to 1:6 is recommended

Medium Renewal: Every 2 to 3 days

Cryopreservation:
Freeze medium: Complete growth medium, 95%; DMSO, 5%
Storage temperature: liquid nitrogen vapor temperature
Culture Conditions:
Temperature: 37°C
STR Profile:
Amelogenin: X,Y
CSF1PO: 11,12
D13S317: 8,12
D16S539: 12,13
D5S818: 10,12
D7S820: 10,11
THO1: 6
TPOX: 8,9
vWA: 17
Population Doubling Time: 38 hrs
Name of Depositor: AF Gazdar, JD Minna
Deposited As: Homo sapiens
Year of Origin: 1981
References:

Brower M, et al. Growth of cell lines and clinical specimens of human non-small cell lung cancer in a serum-free defined medium. Cancer Res. 46: 798-806, 1986. PubMed: 3940644

Gazdar AF, et al. Peripheral airway cell differentiation in human lung cancer cell lines. Cancer Res. 50: 5481-5487, 1990. PubMed: 2386953

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

Sordella R, et al. Gefitinib-sensitizing EGFR mutations in lung cancer activate anti-apoptotic pathways. Science 305: 1163-1167, 2004. PubMed: 15284455