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產品資料

Lec8細胞

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產品名稱: Lec8細胞
產品型號: Lec8
產品展商: HZbscience
產品文檔: 無相關文檔

簡單介紹

Lec8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?jié){菌。主要的污染原因為無菌操作技術不當、操作室環(huán)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(huán)境、與品質良好之細胞來源和培養(yǎng)基配制是減低污染之*好方法。Lec8細胞何時須更換培養(yǎng)基?視細胞生長密度而定,或遵照細胞株基本數(shù)據(jù)上之更換時間,按時更換培養(yǎng)基即可。


Lec8細胞  的詳細介紹

Lec8細胞

ATCC Number: CRL-1737?

細胞形態(tài): 上皮樣

是否是腫瘤細胞: 0

物種來源: 倉鼠

器官來源: 卵巢

運輸方式: 凍存運輸

Lec8細胞數(shù)量: 大量

生長狀態(tài): 單層生長

Designations: Lec8 [originally named Pro-5WgaRVIII3D]

Depositors: P Stanley

Biosafety Level: 1

Shipped: frozen

Medium & Serum: See Propagation

Growth Properties: monolayer

Organism: Cricetulus griseus

Morphology: epithelial


Source: Lec8細胞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. 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 UDP-galactose into the Golgi compartment, and may be useful for studying the role of galactose residues 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 250 cells), and should be cloned if it is desired to use the Pro- marker in complementation studies.

These cells may also be grown as a suspension culture if agitated. Keep the cell concentration between 2 x 104 and 1 x 106 cells/ml.

Propagation: Lec8細胞ATCC complete growth medium: Alpha minimum essential medium, 90%; fetal bovine serum, 10%

Temperature: 37.0°C

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: 1202: Stanley P. Selection of specific wheat germ agglutinin-resistant (WgaR) phenotypes from Chinese hamster ovary cell populations containing numerous lecR genotypes. Mol. Cell. Biol. 1: 687-696, 1981. PubMed: 9279382

22486: Deutscher SL, Hirschberg CB. Lec8細胞Mechanism of galactosylation in the Golgi apparatus. A Chinese hamster ovary cell mutant deficient in translocation of UDP-galactose across Golgi vesicle membranes. J. Biol. Chem. 261: 96-100, 1986. PubMed: 3510203

滬公網(wǎng)安備 31011702004356號

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