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MEG-01细胞

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  • 产品名称:MEG-01细胞
  • 产品型号:MEG-01
  • 产品展商:HZbscience
  • 产品文档:无相关文档
  • 发布时间:2018-08-26
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简单介绍
MEG-01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。MEG-01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。
产品描述

MEG-01细胞

年限: 55 years

运输方式: 冻存运输

细胞类型: 其他细胞类型

是否是肿瘤细胞: 0

物种来源: 人

细胞形态: **样

数量: 大量

ATCC Number: CRL-2021™

相关**: 其他**

生长状态: 混合型生长

Designations: MEG-01

Depositors: M Tekeuchi, MJ Fitzgerald

Biosafety Level: 1

MEG-01细胞Shipped: frozen

Medium & Serum: See Propagation

Growth Properties: mixed, adherent and suspension

Organism: Homo sapiens

Morphology: lymphoblast


Source: Disease: chronic myelogenous leukemia (CML)

Cell Type: megakaryoblast;

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

Antigen Expression: CD41 +; CD61 +; CDw14 +

DNA Profile (STR): Amelogenin: X,Y

CSF1PO: 10

D13S317: 8

D16S539: 9

D5S818: 13

D7S820: 11

THO1: 7

TPOX: 8,11

vWA: 16

Cytogenetic Analysis: MEG-01细胞hyperdiploid; modal number = 56 to 58; the Philadelphia chromosome (Ph1) is present

Age: 55 years

Gender: male

Comments: The MEG-01 cell line was derived in 1983 at the Nagoya University School of Medicine, Nagoya, Japan from bone marrow cells taken from a patient in megakaryoblastic crisis of CML.

The cells are positive for cytoplasmic Factor VIII and surface GPIIb/IIIa, periodic acid - Schiff (PAS) reaction, alpha naphthyl acetate esterase and acid phosphatase.

They are negative for myeloperoxidase, alpha naphthyl butyrate esterase, naphthol AS-D chloroacetate esterase and alkaline phosphatase.

The stain positively with monoclonal antibodies BA-1 (anti B cell, granulocyte), HPL-3 (anti gpIIb/IIIa) and 20.3 (anti monocyte, platelet).

They are negative for other lymphoid and myeloid seris antigens.

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%.

Temperature: 37.0°C

Subculturing: Protocol: MEG-01细胞Subcultures are prepared by scraping the adherent cells into the medium. From the resulting suspension dilute cells to a concentration 1-2 X 10exp5 cells/ml into fresh medium in a new flasks. Keep culture below approximate density of 10exp6 cells/ml.

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

Medium Renewal: 2 to 3 times per week

Subcultures are prepared by scraping the adherent cells into the medium, and diluting the resulting suspension into fresh medium in new flasks.

Doubling Time: 36 to 48 hrs

Related Products: Recommended medium (without the additional supplements or serum described under ATCC Medium):ATCC 30-2001

recommended serum:ATCC 30-2020

References: 23348: Ogura M, et al. Establishment of a novel human megakaryoblastic leukemia cell line, MEG- 01, with positive Philadelphia chromosome. Blood 66: 1384-1392, 1985. MEG-01细胞PubMed: 2998511

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