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MJ细胞

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产品名称: MJ细胞
产品型号: MJ
产品展商: HZbscience
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简单介绍

MJ细胞应如何避免细胞污染,细胞污染的种类可分成**、酵母菌、霉菌、病毒和霉浆菌。主要的污染原因为无菌操作技术不当、操作室环境不佳、污染之血清和污染之细胞等。严格之无菌操作技术、清洁的环境、与品质良好之细胞来源和培养基配制是减低污染之*好方法。MJ细胞何时须更换培养基?视细胞生长密度而定,或遵照细胞株基本数据上之更换时间,按时更换培养基即可。


MJ细胞  的详细介绍

MJ细胞

器官来源: 外周血

年限: 50 years

ATCC Number: CRL-8294™

数量: 大量

相关**: 其他**

生长状态: 悬浮生长

运输方式: 冻存运输

细胞类型: T**细胞

细胞形态: **样

是否是肿瘤细胞: 1

物种来源: 人

Designations: MJ [G11]

MJ细胞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细胞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细胞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细胞Isolation and transmission of human retrovirus (human t-cell leukemia virus). Science 219: 856-859, 1983. PubMed: 6600519

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