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產品資料

NG108-15細胞

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產品名稱: NG108-15細胞
產品型號: NG108-15
產品展商: HZbscience
產品文檔: 無相關文檔

簡單介紹

NG108-15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、病毒和霉漿菌。主要的污染原因為無菌操作技術不當、操作室環境不佳、污染之血清和污染之細胞等。嚴格之無菌操作技術、清潔的環境、與品質良好之細胞來源和培養基配制是減低污染之*好方法。NG108-15細胞何時須更換培養基?視細胞生長密度而定,或遵照細胞株基本數據上之更換時間,按時更換培養基即可。


NG108-15細胞  的詳細介紹
NG108-15細胞

ATCC Number: HB-12317?

相關**: 其他**

細胞類型: 其他細胞類型

是否是腫瘤細胞: 0

物種來源: 小鼠

生長狀態: 貼壁生長

運輸方式: 凍存運輸

細胞形態: 其他

數量: 大量

器官來源: 大腦

NG108-15細胞Designations: NG108-15 [108CC15]

Depositors: Univ. Texas Southwestern Medical Cntr.

Biosafety Level: 1

Shipped: frozen

Medium & Serum: See Propagation

Growth Properties: adherent

Organism: Mus musculus (neuroblastoma); Rattus norvegicus (glioma) deposited as mouse (neuroblastoma); rat (glioma)

Morphology: flat; round; 10 to 100 micrometers diameter


Source: Organ: brain

Disease: glioblastoma; neuroblastoma

Cell Type: somatic cell hybrid

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.

Applications: transfection host NG108-15細胞(Roche Transfection Reagents)

Comments: The NG108-15 cell line, originally named 108CC15, was developed in 1971 by Bernd Hamprecht. [112482]

The line was formed by fusing mouse N18TG2 neuroblastoma cells with rat C6-BU-1 glioma cells in the presence of inactivated Sendai virus. [51493]

Propagation: ATCC complete growth medium: The base medium for this cell line is Dulbecco's Modified Eagle's Medium (GIBCO/InVitrogen Catalog No.12100-061, DMEM without sodium pyruvate ). To make the complete growth medium, add the following components to the base medium:

0.1 mM hypoxanthine (final conc.)

400 nM aminopterin (final conc.)

0.016 mM thymidine (final conc.)

10% fetal bovine serum (final conc.)

1.5 g/L sodium bicarbonate


Temperature: 37.0°C

Atmosphere: air, 95%; carbon dioxide (CO2), 5%

Subculturing: Subcultivation Ratio: A subcultivation ratio of 1:6 to 1:10 is recommended

Medium Renewal: Every 2 to 3 days

Remove medium, and rinse with 0.25% trypsin, 0.03% EDTA solution. Remove the solution and add an additional 1 to 2 ml of trypsin-EDTA solution. NG108-15細胞Allow the flask to sit at room temperature (or at 37C) until the cells detach.

Add fresh culture medium, aspirate and dispense into new culture flasks.

Preservation: Freeze medium: Complete growth medium, 92.5%; DMSO, 7.5%

Storage temperature: liquid nitrogen vapor phase

Related Products: recommended serum:ATCC 30-2020

References: 51492: Hamprecht B. Structural, electrophysiological, biochemical, and pharmacological properties of neuroblastoma-glioma cell hybrids in cell culture. Int. Rev. Cytol. 49: 99-170, 1977. PubMed: 16829

51493: Hamprecht B, et al. Culture and characteristics of hormone-responsive neuroblastoma X glioma hybrid cells. Methods Enzymol. 109: 316-341, 1985. NG108-15細胞PubMed: 2985920

112482: Bernd Hamprecht, personal communication

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