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產(chǎn)品資料

NCCIT細胞

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

簡單介紹

NCCIT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(dāng)、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。NCCIT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。


NCCIT細胞  的詳細介紹

NCCIT細胞

生長狀態(tài): 貼壁生長

運輸方式: 凍存運輸

ATCC Number: CRL-2073?

相關(guān)**: 其他**

是否是腫瘤細胞: 1

物種來源: 人

數(shù)量: 大量

年限: *****

細胞形態(tài): 上皮樣

NCCIT細胞Designations: NCCIT

Depositors: I Damjanov

Biosafety Level: 1

Shipped: frozen

Medium & Serum: See Propagation

Growth Properties: adherent

Organism: Homo sapiens

Morphology: epithelial


Source: Disease: pluripotent embryonal carcinoma; teratocarcinoma

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.

Tumorigenic: NCCIT細胞Yes

DNA Profile (STR): Amelogenin: X

CSF1PO: 10,12

D13S317: 11

D16S539: 9,12

D5S818: 10,13

D7S820: 10

THO1: 7,9

TPOX: 8

vWA: 14,18

Age: *****

Gender: male

Ethnicity: Japanese

Comments: NCCIT細胞NCCIT was established by Shinichi Teshima (National Cancer Institute, Tokyo, Japan) in 1985 from a mediastinal mixed germ cell tumor.

This pluripotent stem cell line is capable of somatic and extraembryonic differentiation.

The undifferentiated cells are equivalent to a stage intermediate between seminoma and embryonal carcinoma.

They will differentiate in response to retinoic acid.

NCCIT cells are negative for keratin.

They are positive for vimentin and placental alkaline phosphatase.

The line was contaminated with mycoplasma, but was cured by the depositor prior to deposit at the ATCC .

Propagation: ATCC complete growth medium: The base medium for this cell line is ATCC-formulated RPMI-1640 Medium, Catalog No. 30-2001. To make the complete growth medium, add the following components to the base medium: fetal bovine serum to a final concentration of 10%.

Subculturing: Subcultivation Ratio: A subcultivation ratio of 1:4 to 1:8 is recommended

Medium Renewal: Add fresh medium at the time of subculture

Remove spent medium, add fresh 0.25% trypsin, 0.03% EDTA solution, rinse and remove trypsin. Let the culture sit at room temperature (or at 37C) for 2 to 5 minutes. NCCIT細胞Add fresh medium, aspirate and dispense into new flasks. Subculture two times weekly.

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

References: 22742: Teshima S, et al. Four new human germ cell tumor cell lines. Lab. Invest. 59: 328-336, 1988. PubMed: 2842544

22743: Damjanov I, et al. Retinoic acid-induced differentiation of the developmentally pluripotent human germ cell tumor-derived cell line, NCCIT. Lab. Invest. 68: 220-232, 1993. PubMed: 7680083

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