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NCI-H128細胞

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產品名稱: NCI-H128細胞
產品型號: NCI-H128
產品展商: HZbscience
產品文檔: 無相關文檔

簡單介紹

NCI-H128細胞應如何避免細胞污染,細胞污染的種類可分成**、酵母菌、霉菌、病毒和霉漿菌。主要的污染原因為無菌操作技術不當、操作室環境不佳、污染之血清和污染之細胞等。嚴格之無菌操作技術、清潔的環境、與品質良好之細胞來源和培養基配制是減低污染之*好方法。NCI-H128細胞何時須更換培養基?視細胞生長密度而定,或遵照細胞株基本數據上之更換時間,按時更換培養基即可。


NCI-H128細胞  的詳細介紹

NCI-H128細胞

是否是腫瘤細胞: 1

物種來源: 人

年限: 60 years

數量: 大量

生長狀態: 漂浮生長

細胞形態: 其他

ATCC Number: HTB-120?

相關**: 小細胞肺癌

器官來源: 肺

運輸方式: 凍存運輸

Designations: NCI-H128 [H128]

Depositors: AF Gazdar

NCI-H128細胞Biosafety Level: 1

Shipped: frozen

Medium & Serum: See Propagation

Growth Properties: floating aggregates

Organism: Homo sapiens

Morphology: floating aggregates


Source: Organ: lung

Disease: carcinoma; small cell lung cancer

Derived from metastatic site: pleural effusion

Permits/Forms: In addition to the MTA mentioned above, other ATCC and/or regulatory permits may be required for the transfer of this ATCC material. Anyone purchasing ATCC material is ultimately responsible for obtaining the permits. Please click here for information regarding the specific requirements for shipment to your location.

Tumorigenic: Yes

DNA Profile (STR): Amelogenin: X

CSF1PO: 10

D13S317: 12

D16S539: 13

D5S818: 9

D7S820: 8,10

THO1: 6,9

TPOX: 8

vWA: 17

Cytogenetic Analysis: NCI-H128細胞There are 2 distinct aneuploid peaks, both have characteristic 3p deletion.

Isoenzymes: AK-1, 1

ES-D, 1

G6PD, A

GLO-I, 1-2

Me-2, 1

PGM1, 1

PGM3, 1

Age: 60 years

Gender: male

Ethnicity: Black

Comments: This cell line is aneuploid.

Will form colonies in soft agar.

It retains small cell carcinoma morphology and ultrastructure as well as APUD cell characteristics.

NCI-H128 cells do well on a rotary shaker flask at 70 to 80 rpm at 37C.

It is normal for cultures of this line to have fairly large amounts of cell debris.

Propagation: ATCC complete growth medium: RPMI 1640 medium, 80%; fetal bovine serum, 20% - OR - Iscove's modified Dulbecco's medium, 80%; fetal bovine serum, 20%

Subculturing: Subcultivation Ratio: A subcultivation ratio of 1:2 to 1:4 is recommended

Medium Renewal: Twice per week

NCI-H128細胞Allow cell aggregates to settle to the bottom of the flask, discard the supernatant medium, disperse the cells with gentle pipetting and dispense into new flasks. Subculture every 6 to 8 days.

Preservation: Culture medium, 90%; DMSO, 10%

Related Products: normal (or near-normal) cell line established from the same patient:ATCC CRL-5947

References: 1805: 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

23036: Gazdar AF, et al. Establishment of continuous, clonable cultures of small-cell carcinoma of lung which have amine precursor uptake and decarboxylation cell properties. Cancer Res. 40: 3502-3507, 1980. PubMed: 6108156

23037: . . Cancer Res. 40: 4556-4563, 1980.

23056: 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

23057: Gazdar AF, et al. Characterization of variant subclasses of cell lines derived from small cell lung cancer having distinctive biochemical, morphological, and growth properties. Cancer Res. 45: 2924-2930, 1985. PubMed: 2985258

23080: 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

32276: Cairns P, et al. NCI-H128細胞Genomic organization and mutation analysis of Hel-N1 in lung cancers with chromosome 9p21 deletions. Cancer Res. 57: 5356-5359, 1997. PubMed: 9393760

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