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Hs 695T細胞

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產品名稱: Hs 695T細胞
產品型號: Hs 695T
產品展商: HZbscience
產品文檔: 無相關文檔

簡單介紹

Hs 695T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?jié){菌。主要的污染原因為無菌操作技術不當、操作室環(huán)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(huán)境、與品質良好之細胞來源和培養(yǎng)基配制是減低污染之*好方法。Hs 695T細胞何時須更換培養(yǎng)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(yǎng)基即可。


Hs 695T細胞  的詳細介紹

Hs 695T細胞

數量: 大量

運輸方式: 凍存運輸

細胞形態(tài): 上皮樣

器官來源: 皮膚

是否是腫瘤細胞: 1

物種來源: 人

生長狀態(tài): 貼壁生長

年限: 26 years *****

ATCC Number: HTB-137?

相關**: 其他**

Designations: Hs 695T

Depositors: RB Owens

Hs 695T細胞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細胞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細胞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細胞Biological properties of human melanoma cells in culture. In Vitro 15: 342-350, 1979. PubMed: 478563

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