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GDM-1细胞

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产品名称: GDM-1细胞
产品型号: GDM-1
产品展商: HZbscience
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简单介绍

GDM-1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。GDM-1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。


GDM-1细胞  的详细介绍

GDM-1细胞

生长状态: 悬浮生长

器官来源: 外周血

细胞类型: 其他细胞类型

是否是肿瘤细胞: 0

物种来源: 人

运输方式: 冻存运输

年限: 66 - 67 years

ATCC Number: CRL-2627™

数量: 大量

相关**: 其他**

细胞形态: **样

GDM-1细胞Designations: GDM-1

Depositors: H Ben-Bassat

Biosafety Level: 1

Shipped: frozen

Medium & Serum: See Propagation

Growth Properties: suspension

Organism: Homo sapiens deposited as human

Morphology: lymphoblast


Source: Organ: peripheral blood

Disease: myelomonoblastic leukemia

Cell Type: monoblast;

Cellular Products: lysozyme [53284]

myeloperoxidase [53284]

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. GDM-1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: complement (C3) [53284]

Fc [53284]

Tumorigenic: No

Antigen Expression: Ia +; myeloid leukemia antigen (M-1) [53284]

Age: 66 - 67 years

Gender: female

Ethnicity: White

Comments: The GDM-1 cell line was established in 1980 from the peripheral blood of a patient with a Philadelphia chromosome negative myeloproliferative disorder, after transformation to acute myelomonoblastic leukemia. [53284]

The cells lack B- and T-cell surface markers including T-associated antigens, E-rosetting capacity, surface and intracytoplasmic immunoglobulins. They are non-specific esterase positive. [53284]

GDM-1细胞The cells are phagocytic for latex beads and iron particles. Exposure to phorbol 12-myristate 13-acetate (TPA) increases the phagocytic activity. TPA also induces macrophage-like differentiation. [53284]

The cells are negative for Epstein-Barr virus nuclear antigen (EBNA-). [53284]

This cell line is a model system for studying myelomonocytic disorders and leukemias.

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: 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 3 - 5 X 10 exp5 viable cells/ml. Maintain cultures at cell concentrations between 3 X 10 exp5 and 3 X 10 exp6 viable cells/ml.

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

Preservation: Freeze medium: Complete growth medium 95%; DMSO, 5%

Storage temperature: liquid nitrogen vapor temperature

Doubling Time: 24 to 36 hrs

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

recommended serum:ATCC 30-2020

References: 53284: Ben-Bassat H, et al. GDM-1细胞Establishment and characterization of a new permanent cell line (GDM-1) from a patient with myelomonoblastic leukemia. Leuk. Res. 6: 743-752, 1982. PubMed: 6296552

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