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NCI-H929细胞

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产品名称: NCI-H929细胞
产品型号: NCI-H929
产品展商: HZbscience
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简单介绍

NCI-H929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。NCI-H929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。


NCI-H929细胞  的详细介绍

NCI-H929细胞

ATCC Number: CRL-9068™

数量: 大量

相关**: 多发性骨髓瘤

细胞类型: B**细胞

是否是肿瘤细胞: 1

物种来源: 人

运输方式: 冻存运输

细胞形态: **样

**类型: IgA kappa (Recent tests for IgA, kappa have not detected the production of IgA; the cells are producing kappa light chain.)

年限: 62 years

器官来源: 骨髓

生长状态: 悬浮生长

Designations: NCI-H929 [H929]

NCI-H929细胞Depositors: National Cancer Institute

Isotype: IgA kappa (Recent tests for IgA, kappa have not detected the production of IgA; the cells are producing kappa light chain.)

Biosafety Level: 1

Shipped: frozen

Medium & Serum: See Propagation

Growth Properties: suspension

Organism: Homo sapiens

Morphology: lymphoblast


Source: Organ: bone marrow

Disease: plasmacytoma; myeloma

Cell Type: B lymphocyte;

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.

Receptors: transferrin

Antigen Expression: PCA-1; CD38 +

DNA Profile (STR): NCI-H929细胞Amelogenin: X

CSF1PO: 11

D13S317: 12

D16S539: 9,13

D5S818: 11,12

D7S820: 10,12

THO1: 9.3

TPOX: 8,11

vWA: 14,15

Cytogenetic Analysis: Near tetraploid. Most copies of chromosome 8 have the 8q+ abnormality.

Age: 62 years

Gender: female

Ethnicity: Caucasian

Comments: This cell line was established from a malignant effusion in a patient with myeloma.

The cells are positive for plasma cell antigen 1 (PCA-1), transferrin receptor, CD38 (T10), but are negative for HLA DR, CALLA and markers of early B cell development.

NCI-H929细胞They are negative for Epstein-Barr virus nuclear antigen (EBNA).

The cells have a rearrangement of the c-myc proto oncogene and express c-myc RNA.

There is also an activated ras allele.

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: 2-mercaptoethanol to a final concentration of 0.05 mM; fetal bovine serum to a final concentration of 10%.

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

Temperature: 37.0°C

Subculturing: Protocol: Cultures can be maintained by the addition of fresh medium or replacement of medium. Alternatively, cultures can be established by centrifugation with subsequent resuspension at 4 X 10(5) viable cells/ml.

Interval: Maintain cultures at cell concentrations between 5 X 10(5) and 1 X 10(6) viable cells/ml.

Medium Renewal: 2 to 3 times per week

Preservation: Freeze medium: Complete growth medium supplemented with 5% (v/v) DMSO

Storage temperature: liquid nitrogen vapor phase

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

recommended serum:ATCC 30-2020

References: 22372: Hollis GF, et al. NCI-H929细胞Complex translocation disrupts c-myc regulation in a human plasma cell myeloma. Mol. Cell. Biol. 8: 124-129, 1988. PubMed: 3275865

23349: Gazdar AF, et al. Establishment and characterization of a human plasma cell myeloma culture having a rearranged cellular myc proto-oncogene. Blood 67: 1542-1549, 1986. PubMed: 2423157

23351: Ernst TJ, et al. Identification of a second transforming gene, rasn, in a human multiple myeloma line with a rearranged c-myc allele. Blood 72: 1163-1167, 1988. PubMed: 3048435

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