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NCI-H676B细胞

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  • 产品名称:NCI-H676B细胞
  • 产品型号:NCI-H676B
  • 产品展商:HZbscience
  • 产品文档:无相关文档
  • 发布时间:2018-07-10
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简单介绍
NCI-H676B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-H676B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。
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NCI-H676B细胞

年限: 63 years

运输方式: 冻存运输

生长状态: 悬浮生长

细胞形态: 上皮样

器官来源: 肺

ATCC Number: HTB-179™

相关**: 腺癌

数量: 大量

是否是肿瘤细胞: 0

物种来源: 人

Designations: NCI-H676B [H676B]

Depositors: AF Gazdar, JD Minna

Biosafety Level: 1

Shipped: frozen

Medium & Serum: See Propagation

NCI-H676B细胞Growth Properties: suspension, multicell aggregates (gland-like clusters in suspension; the viability of cells in clusters is better than the viability of the single cells in the cultures)

Organism: Homo sapiens

Morphology: epithelial


Source: Organ: lung

Disease: adenocarcinoma

Derived from metastatic site: pleural effusion

Cellular Products: mucin

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.

DNA Profile (STR): Amelogenin: X

CSF1PO: 9

D13S317: 10

D16S539: 11,12

D5S818: 11

D7S820: 12

THO1: 9.3

TPOX: 8,11

vWA: 16,19

Cytogenetic Analysis: This is a hypodiploid cell line; modal number = 43; range = 39 to 47. Marker chromosomes consisted of over 70% of the chromosomes in each cell complement. Among the identifiable markers were t(1q8q), der(3)t(3;?)(q29;?), t(2q7q), der(9)t(9;14)(p13;q11) and der(11)t(?q23;?). NCI-H676B细胞All markers had a single copy per cells. The N5, N9, N10, N17, N18, N20, N21 and the X were the only structurally normal chromosomes found. Except for the paired N5, all others had single copies per cell.

Isoenzymes: AK-1, 2

ES-D, 1

G6PD, B

GLO-I, 1-2

Me-2, 0

PGM1, 1-2

PGM3, 2

Age: 63 years

Gender: male

Ethnicity: Caucasian

Comments: The NCI-H676B cell line was derived by A.F. Gazdar and H. Oie in 1984 from the pleural fluid of a patient with adenocarcinoma of the lung taken prior to treatment.

The cells produce a abnormal size p53 mRNA (2.3 kb) as well as the normal size mRNA (2.8 kb).

The line does not exhibit any gross structural DNA abnormalities.

The cells produce mucin, and occasionally signet ring cells are formed.

Propagation: NCI-H676B细胞ATCC complete growth medium: ACL-4 medium (serum-free)

The base medium for this cell line is ATCC formulated DMEM: F12 Medium Catalog No. 30-2006. To make the complete growth medium, add the following components to the base medium:

0.02 mg/ml insulin

0.01 mg/ml transferrin

25 nM sodium selenite (final conc.)

50 nM Hydrocortisone (final conc.)

1 ng/ml Epidermal Growth Factor (do not filter)

0.01 mM ethanolamine (final conc.)

0.01 mM phosphorylethanolamine (final conc.)

100 pM triiodothyronine (final conc.)

0.5% (w/v) bovine serum albumin (final conc.)

0.5 mM sodium pyruvate (final conc.)

extra 2mM L-glutamine (for final conc. of 4.5mM)


Temperature: 37.0°C

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

Subculturing: Protocol: This line grows as aggregates of cells in suspension. Culture can be maintained by addition of medium or by replacement of medium. Alternatively, the cells may be collected by centrifugation and dispersed into fresh medium.

Subcultivation Ratio: NCI-H676B细胞A subcultivation ratio of 1:2 to 1:5 is recommended

Medium Renewal: 2 to 3 times per week

Preservation: Freeze medium: culture medium, 82.5%; fetal bovine serum, 10%; DMSO, 7.5%

Storage temperature: liquid nitrogen vapor phase

Related Products: Recommended medium (without the additional supplements or serum described under ATCC Medium):ATCC 30-2006

References: 1806: Takahashi T, et al. p53: A frequent target for genetic abnormalities in lung cancer. Science 246: 491-494, 1989. PubMed: 2554494

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