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產(chǎn)品資料

C1R-neo細(xì)胞

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產(chǎn)品名稱: C1R-neo細(xì)胞
產(chǎn)品型號(hào): C1R-neo
產(chǎn)品展商: HZbscience
產(chǎn)品文檔: 無相關(guān)文檔

簡(jiǎn)單介紹

C1R-neo細(xì)胞應(yīng)如何避免細(xì)胞污染,細(xì)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?yàn)闊o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(xì)胞等。嚴(yán)格之無菌操作技術(shù)、清潔的環(huán)境、與品質(zhì)良好之細(xì)胞來源和培養(yǎng)基配制是減低污染之*好方法。C1R-neo細(xì)胞何時(shí)須更換培養(yǎng)基?視細(xì)胞生長(zhǎng)密度而定,或遵照細(xì)胞株基本數(shù)據(jù)上之更換時(shí)間,按時(shí)更換培養(yǎng)基即可。


C1R-neo細(xì)胞  的詳細(xì)介紹

C1R-neo細(xì)胞

生長(zhǎng)狀態(tài): 懸浮生長(zhǎng)

細(xì)胞類型: B**細(xì)胞

是否是腫瘤細(xì)胞: 0

物種來源: 人

數(shù)量: 大量

ATCC Number: CRL-2369?

運(yùn)輸方式: 凍存運(yùn)輸

器官來源: 外周血

細(xì)胞形態(tài): **樣

Designations: C1R-neo

Depositors: F Grumet

C1R-neo細(xì)胞Biosafety Level: 2 [Cells contain herpesvirus ]

Shipped: frozen

Medium & Serum: See Propagation

Growth Properties: suspension

Organism: Homo sapiens

Morphology: lymphoblast


Source: Organ: peripheral blood

Cell Type: B lymphoblast; Epstein-Barr virus (EBV) transformed

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.

DNA Profile (STR): Amelogenin: X

CSF1PO: 6,10

D13S317: 11,13

D16S539: 9,13

C1R-neo細(xì)胞D5S818: 10,13

D7S820: 7,12

THO1: 8

TPOX: 8

vWA: 17

Comments: C1R-neo is a stable transfectant cell line established in 1987 by transfection by electroporation of the C1R cell line with a modified neomycin drug-resistant eukaryotic vector, pSP65-Neo. The vector did not carry an insert. [38581]

C1R-neo does not secrete or express HLA B7.

C1R is a human B-cell lymphoblastoid line lacking surface HLA A and B antigens. C1R was derived from Hmy.2 B-LCL by gamma irradiation followed by selection for Class I monoclonal antibodies and complement. [23312]

C1R-neo may be used as a control for C1R-sB7 (CRL-2370), in CTL experiments and for producing control supernatants.

Propagation:C1R-neo細(xì)胞 ATCC complete growth medium: The base medium for this cell line is ATCC-formulated Iscove's Modified Dulbecco's Medium, Catalog No. 30-2005. To make the complete growth medium, add the following components to the base medium: fetal bovine serum to a final concentration of 10%.

Temperature: 37.0°C

Subculturing: Medium Renewal: Add fresh medium every 2 to 3 days (depending on cell density)

Cultures can be maintained by addition of fresh medium or replacement of medium. Alternatively, cultures can be established by centrifugation with subsequent resuspension in fresh medium at 5 X 10(5) viable cells/ml.

Maintain cultures at cell concentrations between 5 X 10(5) and 2 X 10(6) viable cells/ml.

Preservation: culture medium 95%; DMSO, 5%

Related Products: Recommended medium (without the additional supplements or serum described under ATCC Medium):ATCC 30-2005

recommended serum:ATCC 30-2020

parental cell line:ATCC CRL-1993

derived from same cell line:C1R-neo細(xì)胞ATCC CRL-2370

derived from same cell line:ATCC CRL-2371

References: 23312: Storkus WJ, et al. Reversal of natural killing susceptibility in target cells expressing transfected class I HLA genes. Proc. Natl. Acad. Sci. USA 86: 2361-2364, 1989. PubMed: 2784569

38581: Grumet FC, et al. Soluble form of an HLA-B7 class I antigen specifically suppresses humoral alloimmunization. Hum. Immunol. 40: 228-234, 1994. PubMed: 7960967

38582: Hiraki DD, et al. Bioengineered soluble HLA-B7. Genesis, characterization, and occurrence of dimerization. Hum. Immunol. 40: 235-246, 1994. PubMed: 7960968

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