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產(chǎn)品資料

36.5細胞

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產(chǎn)品名稱: 36.5細胞
產(chǎn)品型號: 36.5
產(chǎn)品展商: HZbscience
產(chǎn)品文檔: 無相關(guān)文檔

簡單介紹

36.5細胞應(yīng)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(shù)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(shù)、清潔的環(huán)境、與品質(zhì)良好之細胞來源和培養(yǎng)基配制是減低污染之*好方法。36.5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。


36.5細胞  的詳細介紹

36.5細胞

細胞形態(tài): 上皮樣

生長狀態(tài): 貼壁生長

ATCC Number: CRL-11116?

品系: 129/Sv+c/+p

數(shù)量: 大量

細胞類型: 其他細胞類型

器官來源: 胚胎

是否是腫瘤細胞: 0

物種來源: 小鼠

年限: embryo, blastocyst

36.5細胞運輸方式: 凍存運輸

Designations: 36.5

Depositors: Ontario Cancer Institute

Biosafety Level: 1

Shipped: frozen

Medium & Serum: See Propagation

Growth Properties: adherent

Organism: Mus musculus

Morphology: epithelial


Source: Organ: embryo

Strain: 129/Sv+c/+p

Cell Type: pluripotent embryonic stem cell;

Permits/Forms:36.5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.

Age: embryo, blastocyst

Comments: This line was derived by inserting a construct containing a disrupted murine Lyt-2 (CD8) gene.

The Lyt-2 genes was disrupted by insertion of a plasmid containing a neomycin resistance gene into the first exon of the Lyt-2 gene.

After selection for neomycin resistance and presence of Lyt-2 sequences upstream of the insertion, the 36.5 cell line was established.

This line has been used to produce mice deficient in expression of CD8.

The cells can be maintained in the undifferentiated state by frequent subculture on feeder layers of irradiated (12000 rads) or mitomycin C treated (0.01 mg/ml for 90 minutes) primary mouse embryonic fibroblasts or STO cells.

(see ATCC CRL-1503 or ATCC 56-X, irradiated STO cells).

Propagation: 36.5細胞ATCC complete growth medium: Dulbecco's modified Eagle's medium with 4 mM L-glutamine adjusted to contain 1.5 g/L sodium bicarbonate and 4.5 g/L glucose and supplemented with 0.1 mM 2-mercaptoethanol, 85%; fetal bovine serum, 15%

Temperature: 37.0°C

Subculturing: Subcultivation Ratio: A subcultivation ratio of 1:3 to 1:6 is recommended

Medium Renewal: Every 2 to 3 days

Remove medium and rinse the monolayer with fresh 0.25% trypsin, 0.03% EDTA solution. Remove the trypsin and incubate at 37C until the cells detach (approximately 10 minutes). Add fresh medium, aspirate and dispense onto fresh feeder layer cultures.

Preservation: culture medium 95%; DMSO, 5%

Related Products: Recommended medium (without the additional supplements or serum described under ATCC Medium):ATCC 30-2002

recommended serum:ATCC 30-2020

feeder layer cells:ATCC 56-X

References: 22100: Mak TW. 36.5細胞Mutant mouse lacking CD8 surface marker. US Patent 5,530,178 dated Jun 25 1996

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