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產(chǎn)品資料

SW 156細胞

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產(chǎn)品名稱: SW 156細胞
產(chǎn)品型號: SW 156
產(chǎn)品展商: HZbscience
產(chǎn)品文檔: 無相關文檔

簡單介紹

SW 156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。SW 156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。


SW 156細胞  的詳細介紹

SW 156細胞

器官來源: 腎臟

細胞形態(tài): 上皮樣

生長狀態(tài): 貼壁生長

運輸方式: 凍存運輸

數(shù)量: 大量

是否是腫瘤細胞: 1

物種來源: 人

ATCC Number: CRL-2175?

相關**: 其他**

SW 156細胞年限: 75 years

Designations: SW 156 [SW-156, SW156]

Depositors: W McCombs

Biosafety Level: 1

Shipped: frozen

Medium & Serum: See Propagation

Growth Properties: adherent

Organism: Homo sapiens

Morphology: epithelial


Source: Organ: kidney

Disease: hypernephroma

Permits/Forms: SW 156細胞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.

Restrictions: These cells are distributed for research purposes only. The Scott and White Clinic releases the line subject to the following: 1) The cells or products derived from them must not be sold or used for commercial purposes. Nor can the cells be distributed to third parties for purpose of sale, or producing for sale, cells or their products. Commercial interests are the exclusive property of the Scott and White Clinic. 2) Any proposed commercial use of these cells or products produced by them must first be negotiated with the Scott and White Clinic, 2401 S. 31 Street, Temple, Texas 76508. Telephone (817) 774-2432

Antigen Expression: Blood Type O; Rh +

Age: 75 years

Gender: male

Ethnicity: Caucasian

Comments: The SW 156 line was established in 1972 by A. Leibovitz from a hypernephroma.

SW 156細胞Propagation: ATCC complete growth medium: Leibovitz's L-15 medium with 2mM L-glutamine, 90%; fetal bovine serum, 10%

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

Medium Renewal: 2 to 3 times per week

Remove spent medium, add fresh 0.25% trypsin, 0.03% EDTA solution, rinse and remove trypsin.

Add fresh trypsin solution (1 to 2 ml), and let the culture sit at room temperature (or at 37C) until the cells detach.

Add fresh medium, aspirate and dispense into new flasks.

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

References: 22536: Fogh J, et al. SW 156細胞Absence of HeLa cell contamination in 169 cell lines derived from human tumors. J. Natl. Cancer Inst. 58: 209-214, 1977. PubMed: 833871

24381: Fogh J. Cultivation, characterization, and identification of human tumor cells with emphasis on kidney, testis, and bladder tumors. Natl. Cancer Inst. Monogr. 49: 5-9, 1978. PubMed: 571047

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