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COLO 829細胞

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產品名稱: COLO 829細胞
產品型號: COLO 829
產品展商: HZbscience
產品文檔: 無相關文檔

簡單介紹

COLO 829細胞應如何避免細胞污染,細胞污染的種類可分成**、酵母菌、霉菌、病毒和霉漿菌。主要的污染原因為無菌操作技術不當、操作室環境不佳、污染之血清和污染之細胞等。嚴格之無菌操作技術、清潔的環境、與品質良好之細胞來源和培養基配制是減低污染之*好方法。COLO 829細胞何時須更換培養基?視細胞生長密度而定,或遵照細胞株基本數據上之更換時間,按時更換培養基即可。


COLO 829細胞  的詳細介紹

COLO 829細胞

年限: 45 years

生長狀態: 貼壁生長

器官來源: 皮膚

運輸方式: 凍存運輸

細胞形態: 成纖維樣

ATCC Number: CRL-1974?

相關**: 惡性黑色素瘤

數量: 大量

是否是腫瘤細胞: 1

物種來源: 人

Designations: COLO 829

Depositors: GE Moore

COLO 829細胞Biosafety Level: 1

Shipped: frozen

Medium & Serum: See Propagation

Growth Properties: adherent

Organism: Homo sapiens

Morphology: fibroblast


Source: Organ: skin

Disease: malignant melanoma

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): COLO 829細胞Amelogenin: X

CSF1PO: 11

D13S317: 11,12

D16S539: 13

D5S818: 11

D7S820: 8,10

THO1: 10

TPOX: 8,11

vWA: 17,19

Age: 45 years

Gender: male

Ethnicity: Caucasian

Comments: The COLO 829 cell line was established by G.E. Moore from a biopsy specimen taken from a patient prior to chemotherapy for metastatic melanoma.

COLO 829細胞A cell line was also produced from peripheral blood B cells, and is available as COLO 829BL (ATCC CRL-1980).

Early passages of COLO 829 still contain a small percentage of melanin producing cells.

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: Subcultivation Ratio: A subcultivation ratio of 1:3 to 1:6 is recommended

Medium Renewal: 2 to 3 times per week

Remove medium, and rinse with 0.25% trypsin, 0.03% EDTA solution. Remove the solution and add an additional 1 to 2 ml of trypsin-EDTA solution. Allow the flask to sit at room temperature (or at 37C) until the cells detach.

Add fresh culture medium, aspirate and dispense into new culture flasks.

Preservation: culture medium 95%; DMSO, 5%

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

recommended serum:ATCC 30-2020

normal (or near-normal) cell line established from the same patient:COLO 829細胞ATCC CRL-1980

滬公網安備 31011702004356號

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