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NCI-H510A細(xì)胞

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產(chǎn)品名稱: NCI-H510A細(xì)胞
產(chǎn)品型號(hào): NCI-H510A
產(chǎn)品展商: HZbscience
產(chǎn)品文檔: 無(wú)相關(guān)文檔

簡(jiǎn)單介紹

NCI-H510A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。NCI-H510A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。


NCI-H510A細(xì)胞  的詳細(xì)介紹

NCI-H510A細(xì)胞

生長(zhǎng)狀態(tài): 混合型生長(zhǎng)

運(yùn)輸方式: 凍存運(yùn)輸

數(shù)量: 大量

器官來(lái)源: 肺

細(xì)胞形態(tài): 上皮樣

ATCC Number: HTB-184?

相關(guān)**: 其他**

年限: 56 years

是否是腫瘤細(xì)胞: 1

物種來(lái)源: 人

NCI-H510A細(xì)胞Designations: NCI-H510A [H510A, NCI-H510]

Depositors: AF Gazdar, JD Minna

Biosafety Level: 1

Shipped: frozen

Medium & Serum: See Propagation

Growth Properties: mixed, adherent and suspension

Organism: Homo sapiens

Morphology: epithelial


Source: Organ: lung

Disease: carcinoma; small cell lung cancer; extrapulmonary origin

Derived from metastatic site: adrenal gland

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. NCI-H510A細(xì)胞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.

Applications: The NCI-H510A cell line was derived by D. Carney, A.F. Gazdar and associates in 1982 from an adrenal metastasis in an ***** male patient.

The cells produce easily detectable p53 mRNA at levels comparable to those in normal lung tissue.

The line does not exhibit any gross structural DNA abnormalities.

The cells express elevated levels of four biochemical markers of SCLC (neuron specific enolase, the brain isoenzyme of creatine kinase, L-DOPA decarboxylase and bombesin-like immunoreactivity.

Tumorigenic: Yes

DNA Profile (STR): Amelogenin: X

CSF1PO: 10,12

D13S317: 11,12

D16S539: 13

D5S818: 9,12

THO1: 7,9.3

TPOX: 8

vWA: 15

Cytogenetic Analysis: NCI-H510A細(xì)胞hypotriploid; modal number = 54; range = 46 to 57. Twenty to 25 marker chromosomes were common to all cells. These included t(13q21q), der(1)t(1;21)(p36.1;q11), der(7)t(7;7)(p22;q22), 11p+, 12p+, and 15p+. Neither DM nor HSR were detected; structurally normal N1, N2, N13 and N21 were absent. Generally, there were 3 copies of both F group chromosomes; the X chromosomes were paired, and structurally normal Y chromosome was not found.

Age: 56 years

Gender: male

Ethnicity: Caucasian

Comments: The NCI-H510A cell line was derived by D. Carney, A.F. Gazdar and associates in 1982 from an adrenal metastasis in an ***** male patient.

The cells produce easily detectable p53 mRNA at levels comparable to those in normal lung tissue.

The line does not exhibit any gross structural DNA abnormalities.

The cells express elevated levels of four biochemical markers of SCLC (neuron specific enolase, the brain isoenzyme of creatine kinase, L-DOPA decarboxylase and bombesin-like immunoreactivity.

Propagation: ATCC complete growth medium: The base medium for this cell line is ATCC-formulated F-12K Medium, Catalog No. 30-2004. To make the complete growth medium, add the following components to the base medium: fetal bovine serum to a final concentration of 10%.

Atmosphere: air, 95%; carbon dioxide (CO2), 5%

Temperature: 37.0°C

Subculturing: Protocol: This line grows as a mixture of cells in suspension and adherent cells. Subcultures can be prepared by scraping the adherent cells into the medium, collecting the cells by centrifugation, resuspending in fresh medium and dispensing into new flasks.

Subcultivation Ratio: NCI-H510A細(xì)胞A subcultivation ratio of 1:3 to 1:8 is recommended

Medium Renewal: 2 to 3 times per week

Preservation: Freeze medium: culture medium, 92.5%; DMSO, 7.5%

Storage temperature: liquid nitrogen vapor phase

References: 1806: Takahashi T, et al. p53: A frequent target for genetic abnormalities in lung cancer. Science 246: 491-494, 1989. PubMed: 2554494

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

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