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HT-1197細胞

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產品名稱: HT-1197細胞
產品型號: HT-1197
產品展商: HZbscience
產品文檔: 無相關文檔

簡單介紹

HT-1197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。HT-1197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。


HT-1197細胞  的詳細介紹

HT-1197細胞

年限: 44 years

生長狀態: 貼壁生長

運輸方式: 凍存運輸

ATCC Number: CRL-1473?

相關**: 腫瘤

器官來源: 膀胱

數量: 大量

是否是腫瘤細胞: 1

物種來源: 人

Designations: HT-1197

Depositors: S Rasheed

HT-1197細胞Biosafety Level: 1

Shipped: frozen

Medium & Serum: See Propagation

Growth Properties: adherent

Organism: Homo sapiens

Morphology:

Source: Organ: urinary bladder

Disease: carcinoma

Cellular Products: fibrinolytic activity

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.

Tumorigenic: Yes

Isoenzymes: G6PD, B

Age: 44 years

Gender: HT-1197細胞male

Ethnicity: Caucasian

Comments: The cells will also grow in soft agar.

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%.

Subculturing: Protocol: Volumes used in this protocol are for 75 cm2 flask; proportionally reduce or increase amount of dissociation medium for culture vessels of other sizes. 1. Remove and discard culture medium.2. Briefly rinse the cell layer with 0.25% (w/v) Trypsin-0.53mM EDTA solution to remove all traces of serum, which contains trypsin inhibitor.3. HT-1197細胞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.4. Add 6.0 to 8.0 ml of complete growth medium and aspirate cells by gently pipetting. 5. Add appropriate aliquots of the cell suspension to new culture vessels. 6. Incubate cultures at 37?C.

Subcultivation Ratio: Subcultivation Ratio: 1:5 to 1:10

Medium Renewal: HT-1197細胞Twice per week

Preservation: Storage temperature: liquid nitrogen vapor phase

Related Products: purified DNA:ATCC CRL-1473D

References: 22538: Rasheed S, et al. Human bladder carcinoma: characterization of two new tumor cell lines and search for tumor viruses. J. Natl. Cancer Inst. 58: 881-890, 1977. PubMed: 191628

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