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A-427細(xì)胞

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產(chǎn)品名稱: A-427細(xì)胞
產(chǎn)品型號(hào): A-427
產(chǎn)品展商: HZbscience
產(chǎn)品文檔: 無(wú)相關(guān)文檔

簡(jiǎn)單介紹

A-427細(xì)胞應(yīng)如何避免細(xì)胞污染,細(xì)胞污染的種類可分成**、酵母菌、霉菌、病毒和霉?jié){菌。主要的污染原因?yàn)闊o(wú)菌操作技術(shù)不當(dāng)、操作室環(huán)境不佳、污染之血清和污染之細(xì)胞等。嚴(yán)格之無(wú)菌操作技術(shù)、清潔的環(huán)境、與品質(zhì)良好之細(xì)胞來(lái)源和培養(yǎng)基配制是減低污染之*好方法。A-427細(xì)胞何時(shí)須更換培養(yǎng)基?視細(xì)胞生長(zhǎng)密度而定,或遵照細(xì)胞株基本數(shù)據(jù)上之更換時(shí)間,按時(shí)更換培養(yǎng)基即可。


A-427細(xì)胞  的詳細(xì)介紹

A-427細(xì)胞

是否是腫瘤細(xì)胞: 1

物種來(lái)源: 人

運(yùn)輸方式: 凍存運(yùn)輸

年限: 52 years

器官來(lái)源: 肺

細(xì)胞形態(tài): 上皮樣

ATCC Number: HTB-53?

相關(guān)**: 腫瘤

數(shù)量: 大量

生長(zhǎng)狀態(tài): 貼壁生長(zhǎng)

Designations: A-427

A-427細(xì)胞Depositors: DJ Giard

Biosafety Level: 1

Shipped: frozen

Medium & Serum: See Propagation

Growth Properties: adherent

Organism: Homo sapiens

Morphology: epithelial


Source: Organ: lung

Disease: carcinoma

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,Y

CSF1PO: 10,12

A-427細(xì)胞D13S317: 11,12

D16S539: 11,13

D5S818: 12

D7S820: 8,12

THO1: 9

TPOX: 8,11

vWA: 17

Cytogenetic Analysis: at passage 60, hypotriploid to hypertriploid with abnormalities including dicentrics, minutes and large subtelocentric marker

Isoenzymes: AK-1, 2

ES-D, 1

G6PD, B

GLO-I, 1

PGM1, 1-2

PGM3, 1

Age: 52 years

Gender: male

Ethnicity: Caucasian

Comments: A-427細(xì)胞The A-427 line was derived by D.J. Giard, as indicated in the description for ATCC HTB-41.

Propagation: ATCC complete growth medium: The base medium for this cell line is ATCC-formulated Eagle's Minimum Essential Medium, Catalog No. 30-2003. To make the complete growth medium, add the following components to the base medium: fetal bovine serum to a final concentration of 10%.

Temperature: 37.0°C

Subculturing: Protocol: Remove medium, and rinse the monolayer with fresh 0.25% trypsin, 0.53 mM EDTA solution. Remove the trypsin, add fresh trypsin and let the culture sit at room temperature (or at 37C) until the cells detach (about 10 minutes). Add fresh medium, aspirate and dispense into new flasks.

Interval: every 6 to 8 days

Subcultivation Ratio: 1:2 to 1:6

Medium Renewal: Twice per week

Preservation: Freeze medium: culture medium, 95%; DMSO, 5%

Storage temperature: liquid nitrogen vapor phase

References: 22536: 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

22539: Fogh J, 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: 327080

23218: Giard DJ, et al. A-427細(xì)胞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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