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HT-1197细胞

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产品名称: HT-1197细胞
产品型号: HT-1197
产品展商: HZbscience
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简单介绍

HT-1197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。HT-1197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。


HT-1197细胞  的详细介绍

HT-1197细胞

年限: 44 years

生长状态: 贴壁生长

运输方式: 冻存运输

ATCC Number: CRL-1473™

相关**: 肿瘤

器官来源: 膀胱

数量: 大量

是否是肿瘤细胞: 1

物种来源: 人

Designations: HT-1197

Depositors: S Rasheed

HT-1197细胞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细胞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细胞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细胞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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