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SW 1353细胞

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产品名称: SW 1353细胞
产品型号: SW 1353
产品展商: HZbscience
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简单介绍

SW 1353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。SW 1353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。


SW 1353细胞  的详细介绍

SW 1353细胞

年限: 72 years

运输方式: 冻存运输

ATCC Number: HTB-94™

相关**: 其他**

数量: 大量

细胞形态: 成纤维样

生长状态: 贴壁生长

器官来源: 骨

是否是肿瘤细胞: 1

物种来源: 人

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

Depositors: A Leibovitz

SW 1353细胞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细胞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细胞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细胞(without the additional supplements or serum described under ATCC Medium):ATCC 30-2008

recommended serum:ATCC 30-2020

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