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Hs 695T细胞

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产品名称: Hs 695T细胞
产品型号: Hs 695T
产品展商: HZbscience
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简单介绍

Hs 695T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。Hs 695T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。


Hs 695T细胞  的详细介绍

Hs 695T细胞

数量: 大量

运输方式: 冻存运输

细胞形态: 上皮样

器官来源: 皮肤

是否是肿瘤细胞: 1

物种来源: 人

生长状态: 贴壁生长

年限: 26 years *****

ATCC Number: HTB-137™

相关**: 其他**

Designations: Hs 695T

Depositors: RB Owens

Hs 695T细胞Biosafety Level: 1

Shipped: frozen

Medium & Serum: See Propagation

Growth Properties: adherent

Organism: Homo sapiens

Morphology: epithelial


Source: Organ: skin

Disease: melanoma, amelanotic

Derived from metastatic site: lymph node

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.

Isolation: Isolation date: 1973

Tumorigenic: Yes

DNA Profile (STR): Hs 695T细胞Amelogenin: X,Y

CSF1PO: 11

D13S317: 12

D16S539: 9,13

D5S818: 9

D7S820: 9,10

THO1: 6

TPOX: 8

vWA: 18

Cytogenetic Analysis: (P19-40) mode = 52; Y chromosome present

Isoenzymes: AK-1, 1

ES-D, 1

G6PD, B

GLO-I, 1

Me-2, 0

PGM1, 1

PGM3, 1

Age: 26 years *****

Gender: male

Ethnicity: Caucasian

Comments: Hs 695T细胞Hs 695T was isolated in 1973 from the lymph node metastasis of an amelanotic melanoma by A. Creasey et al. The cells had a doubling time of approximately 48 hours at passages 19 through 40 and grew moderately in semi-solid medium.

Propagation: ATCC complete growth medium: The base medium for this cell line is ATCC-formulated Eagle's Minimum Essential Medium, Catalog No. 30-2003. 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: Protocol:

Remove and discard culture medium.

Briefly rinse the cell layer with 0.25% (w/v) Trypsin- 0.53 mM EDTA solution to remove all traces of serum which contains trypsin inhibitor.

Add 2.0 to 3.0 ml of Trypsin-EDTA solution to flask and observe cells under an inverted microscope until cell layer is dispersed (usually within 5 to 15 minutes).

Note: To avoid clumping do not agitate the cells by hitting or shaking the flask while waiting for the cells to detach. Cells that are difficult to detach may be placed at 37�C to facilitate dispersal.

Add 6.0 to 8.0 ml of complete growth medium and aspirate cells by gently pipetting.

Add appropriate aliquots of the cell suspension to new culture vessels.

Incubate cultures at 37�C.


Subcultivation Ratio: A subcultivation ratio of 1:2 to 1:4 is recommended

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 30-2003

recommended serum:ATCC 30-2020

References: 22658: Creasey AA, et al. Hs 695T细胞Biological properties of human melanoma cells in culture. In Vitro 15: 342-350, 1979. PubMed: 478563

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