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產(chǎn)品資料

Lec2細(xì)胞

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產(chǎn)品名稱: Lec2細(xì)胞
產(chǎn)品型號(hào): Lec2
產(chǎn)品展商: HZbscience
產(chǎn)品文檔: 無相關(guān)文檔

簡單介紹

Lec2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)格之無菌操作技術(shù)、清潔的環(huán)境、與品質(zhì)良好之細(xì)胞來源和培養(yǎng)基配制是減低污染之*好方法。Lec2細(xì)胞何時(shí)須更換培養(yǎng)基?視細(xì)胞生長密度而定,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。


Lec2細(xì)胞  的詳細(xì)介紹

Lec2細(xì)胞

細(xì)胞形態(tài): 上皮樣

運(yùn)輸方式: 凍存運(yùn)輸

ATCC Number: CRL-1736?

是否是腫瘤細(xì)胞: 0

物種來源: 倉鼠

數(shù)量: 大量

器官來源: 卵巢

生長狀態(tài): 單層(少量懸浮)

Lec2細(xì)胞Designations: Lec2 [originally named Pro-5WgaRII6A]

Depositors: P Stanley

Biosafety Level: 1

Shipped: frozen

Medium & Serum: See Propagation

Growth Properties: monolayer or suspension

Organism: Cricetulus griseus

Morphology: epithelial


Source: Organ: ovary

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. Lec2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.

Gender: female

Comments: This line is a mutant clone derived from the parental CHO clone Pro-5 (a proline auxotroph, see ATCC CRL-1781) by selection for resistance to wheat germ agglutinin.

The cells exhibit a drastic reduction in the transport of CMP-sialic acid into the Golgi compartment, and may be useful for studying the role of sialic acid in the function and compartmentalization of glycosylated macromolecules.

The cells are proline auxotrophs and must be grown in a medium that contains proline (40 mg/L).

The population contains Pro+ revertants at high frequency (approximately 1 in 25 cells), and should be cloned if it is desired to use the Pro- marker in complementation studies.

Propagation: Lec2細(xì)胞ATCC complete growth medium: Alpha minimum essential medium, 90%; fetal bovine serum, 10%

Subculturing: Protocol: Remove medium, add fresh 0.25% trypsin, let sit for 2 to 3 minutes, remove trypsin and let the culture sit at room temperature for 5 to 10 minutes or until the cells detach. Add fresh medium, aspirate and dispense into new flasks.

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

Medium Renewal: 2 to 3 times per week

References: 22626: Deutscher SL, et al. Translocation across Golgi vesicle membranes: a CHO glycosylation mutant deficient in CMP-sialic acid transport. Cell 39: 295-299, 1984. PubMed: 6498937

58070: Stanley P, Siminovitch L. Complementation between mutants of CHO cells resistant to a variety of plant lectins. Somatic Cell Genet. 3: 391-405, 1977. Lec2細(xì)胞PubMed: 601679

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