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產品資料

SW 1353細胞

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產品名稱: SW 1353細胞
產品型號: SW 1353
產品展商: HZbscience
產品文檔: 無相關文檔

簡單介紹

SW 1353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。SW 1353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。


SW 1353細胞  的詳細介紹

SW 1353細胞

年限: 72 years

運輸方式: 凍存運輸

ATCC Number: HTB-94?

相關**: 其他**

數量: 大量

細胞形態: 成纖維樣

生長狀態: 貼壁生長

器官來源: 骨

是否是腫瘤細胞: 1

物種來源: 人

Designations: SW 1353 [SW 1353, SW-1353]

Depositors: A Leibovitz

SW 1353細胞Biosafety Level: 1

Shipped: frozen

Medium & Serum: See Propagation

Growth Properties: adherent

Organism: Homo sapiens

Morphology: fibroblast


Source: Organ: bone

Disease: chondrosarcoma

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 (Roche Transfection Reagents)

Antigen Expression: Blood type O-

DNA Profile (STR): Amelogenin: X

CSF1PO: 12

D13S317: 12,13

D16S539: 11,12

D5S818: 10,11

D7S820: 9,11

THO1: 6,9

TPOX: 8,11

vWA: 16,17

Cytogenetic Analysis: SW 1353細胞hyperdiploid 47, XX, +7; Except for the trisomic N7 no other chromosome markers are evident

Isoenzymes: AK-1, 1

ES-D, 2

G6PD, B

GLO-I, 2

PGM1, 1

PGM3, 2

Age: 72 years

Gender: female

Ethnicity: Caucasian

Comments: The SW 1353 cell line was initiated by A. Leibovitz at the Scott and White Clinic, Temple, Texas in 1977 from a primary grade II chondrosarcoma of the right humerus obtained from a 72 year old female Caucasian.

SW 1353細胞The initial culture medium was L-15 containing cortisone and insulin plus 10% fetal bovine serum and antibiotics.

A frozen ampule at passage 12 was received at the ATCC in January, 1982.

Propagation: ATCC complete growth medium: The base medium for this cell line is ATCC-formulated Leibovitz's L-15 Medium, Catalog No. 30-2008. 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

Atmosphere: air, 100%

Subculturing: Protocol: 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.

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

Medium Renewal: 2 to 3 times per week

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

Storage temperature: liquid nitrogen vapor temperature

Related Products: Recommended medium SW 1353細胞(without the additional supplements or serum described under ATCC Medium):ATCC 30-2008

recommended serum:ATCC 30-2020

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