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產(chǎn)品資料

Sol8細胞

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產(chǎn)品名稱: Sol8細胞
產(chǎn)品型號: Sol8
產(chǎn)品展商: HZbscience
產(chǎn)品文檔: 無相關文檔

簡單介紹

Sol8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(zhì)良好之細胞來源和培養(yǎng)基配制是減低污染之*好方法。Sol8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。


Sol8細胞  的詳細介紹

Sol8細胞


品系: C3H

組織來源: skeletal muscle

ATCC Number: CRL-2174?

運輸方式: 凍存運輸

數(shù)量: 大量

細胞類型: 其他細胞類型

生長狀態(tài): 貼壁生長

細胞形態(tài): 成纖維樣

是否是腫瘤細胞: 0

物種來源: 小鼠

年限: 4 weeks

Sol8細胞Designations: Sol8

Depositors: R Bassel-Duby

Biosafety Level: 1

Shipped: frozen

Medium & Serum: See Propagation

Growth Properties: adherent

Organism: Mus musculus

Morphology: fibroblast

Sol8細胞

Source: Tissue: skeletal muscle

Strain: C3H

Cell Type: myoblast myoblast;

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. Sol8細胞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.

Age: 4 weeks

Comments: Sol8 is a myogenic cell line isolated by Daubas et al. from primary cultures of soleus muscle taken from the leg of a normal C3H mouse.

The cells were split two times and then cloned by limiting dilution.

Sol8 cells will differentiate into myotubes with serum deprivation.

They have a phenotype similar to slow twitch fibers.

Note: do not allow the cells to become confluent.

The myoblast component of the population will rapidly become depleted if the culture becomes confluent.

Propagation: ATCC complete growth medium: The base medium for this cell line is ATCC-formulated Dulbecco's Modified Eagle's Medium, Catalog No. 30-2002. To make the complete growth medium, add the following components to the base medium: fetal bovine serum to a final concentration of 20%.

Subculturing: Subcultivation Ratio: A subcultivation ratio of 1:8 to 1:12 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.

Subculture at 50% of confluence.

Preservation: Sol8細胞Culture medium, 95%; DMSO, 5%

Doubling Time: 16 to 18 hrs

References: 23248: Daubas P, et al. Functional activity of the two promoters of the myosin alkali light chain gene in primary muscle cell cultures: comparison with other muscle gene promoters and other culture systems. Nucleic Acids Res. 16: 1251-1271, 1988. PubMed: 2894633


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