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MJ細胞

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產品名稱: MJ細胞
產品型號: MJ
產品展商: HZbscience
產品文檔: 無相關文檔

簡單介紹

MJ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。MJ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。


MJ細胞  的詳細介紹

MJ細胞

器官來源: 外周血

年限: 50 years

ATCC Number: CRL-8294?

數量: 大量

相關**: 其他**

生長狀態: 懸浮生長

運輸方式: 凍存運輸

細胞類型: T**細胞

細胞形態: **樣

是否是腫瘤細胞: 1

物種來源: 人

Designations: MJ [G11]

MJ細胞Depositors: President and Fellows of Harvard College

Biosafety Level: 2 [Cells Contain RETROVIRUS ]

Shipped: frozen

Medium & Serum: See Propagation

Growth Properties: suspension

Organism: Homo sapiens

Morphology: lymphoblast


Source: Organ: peripheral blood

Disease: cutaneous T cell lymphoma; mycosis fungoides

Cell Type: T lymphocyte;

Cellular Products: HTLV-I

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. MJ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.

Receptors: interleukin 2 (IL-2)

Antigen Expression: CD2 +; CD3 +; CD4 +

DNA Profile (STR): Amelogenin: X,Y

CSF1PO: 11,12

D13S317: 12,14

D16S539: 11,12

D5S818: 11,13

D7S820: 8,11

THO1: 6,7

TPOX: 8,11

vWA: 15,17

Age: 50 years

Gender: male

Ethnicity: Caucasian

Comments: MJ細胞This line was established by Popovic et al. in 1983 from peripheral blood of a patient with CTCL.

The cells produce Human T cell Leukemia virus (HTLV-I) and HTLV related antigens.

The cells express a cell surface glycoprotein of 61000 daltons (45000 dalton when not glycosylated) that is characteristic of HTLV infection.

Propagation: ATCC complete growth medium: Iscove's modified Dulbecco's medium, 80%; fetal bovine serum, 20%

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

Temperature: 37.0°C

Subculturing: Protocol: Pellet cells by centrigation, save one third of the spent medium and to two volumes of fresh medium. Resuspend the cell pellet in the mixture and dispense into new flasks. Establish new cultures at about 1 X 10(6) cells/ml.

Subcultivation Ratio: A subcultivation ratio of 1:2 to 1:3 is recommended

Medium Renewal: Twice per week

References: 4002: Essex ME, Lee TH. Method and products for detection of human T cell leukemia virus. US Patent 4,743,678 dated May 10 1988

22945: Popovic M, et al. MJ細胞Isolation and transmission of human retrovirus (human t-cell leukemia virus). Science 219: 856-859, 1983. PubMed: 6600519

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