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SW 1271細胞

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產品名稱: SW 1271細胞
產品型號: SW 1271
產品展商: HZbscience
產品文檔: 無相關文檔

簡單介紹

SW 1271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。SW 1271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。


SW 1271細胞  的詳細介紹

SW 1271細胞

細胞形態: 上皮樣

數量: 大量

年限: 69 years

是否是腫瘤細胞: 1

物種來源: 人

運輸方式: 凍存運輸

生長狀態: 貼壁生長

ATCC Number: CRL-2177?

器官來源: 肺

相關**: 小細胞肺癌

Designations: SW 1271 [SW-1271, SW1271]

SW 1271細胞Depositors: W McCombs

Biosafety Level: 1

Shipped: frozen

Medium & Serum: See Propagation

Growth Properties: adherent

Organism: Homo sapiens

Morphology: epithelial


Source: Organ: lung

Disease: carcinoma; small cell lung cancer

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.

Isolation: Isolation date: 1976

Antigen Expression: Blood Type A; Rh +

DNA Profile (STR): SW 1271細胞Amelogenin: X

CSF1PO: 11

D13S317: 13

D16S539: 11,12

D5S818: 12

D7S820: 9,12

THO1: 7,8

TPOX: 8

vWA: 17,20

Age: 69 years

Gender: male

Ethnicity: Caucasian

Propagation: ATCC complete growth medium: The base medium for this cell line is ATCC-formulated Leibovitz's L-15 Medium, Catalog No. 30-2008. 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, 100%

Temperature: 37.0°C

Subculturing: SW 1271細胞Protocol:

Remove and discard culture medium.

Briefly rinse the cell layer with 0.25% (w/v) Trypsin - 0.53% mM EDTA solution to remove all traces of serum which contains trypsin inhibitor.

Add 2.0 to 3.0 ml of Trypsin-EDTA solution to flask and observe cells under an inverted microscope until cell layer is dispersed (usually with 5 to 15 minutes).

Note: To avoid clumping do not agitate the cells by hitting or shaking the flask while waiting for the cells to detach. Cells that are difficult to detach may be placed at 37C to facilitate dispersal.

Add 6.0 to 8.0 ml of complete growth medium and aspirate cells by gently pipetting.

Add appropriate aliquots of cell suspension to new culture vessels.

Place culture vessels in incubators at 37C.


Subcultivation Ratio: A subcultivation ratio of 1:4 to 1:6 is recommended

Medium Renewal: 2 to 3 times per week

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

Storage temperature: SW 1271細胞liquid nitrogen vapor phase

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