KATO III 人胃癌细胞-细胞株/菌种-试剂-生物在线
KATO III 人胃癌细胞

KATO III 人胃癌细胞

商家询价

产品名称: KATO III 人胃癌细胞

英文名称: KATO III

产品编号: HTB-103

产品价格: 0

产品产地: 美国

品牌商标: ATCC

更新时间: null

使用范围: null

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 HTB-103 KATO III 人胃癌细胞

Organism Homo sapiens, human
Tissue
stomach:derived from metastatic pleural effusion; supraclavicular and axillary lymph nodes and Douglas cul-de-sac
Product Format frozen
Morphology spherical
Culture Properties mixed, adherent and suspension
Biosafety Level 1
Disease gastric carcinoma
Age 55 years adult
Gender male
Ethnicity Asian                  HTB-103 KATO III 人胃癌细胞
Storage Conditions liquid nitrogen vapor phase
Karyotype The stemline chromosome number is hypotetraploid with the 2S component occurring at 6.2%. Nine markers were common to most S metaphases, four markers were less frequent. One (occasionally 2 copies) homogenous staining region (HSR) (t(11;HSR) was present in all metaphases examined, but no double minutes (DM) were detected.
Clinical Data
55 years adult
Asian
male
Tumorigenic Yes
Effects
Yes, in cheek pouches of anti thymocyte serum treated hamsters
No, in nude mice
Complete Growth Medium The base medium for this cell line is ATCC-formulated Iscoves Modified Dulbeccos Medium, Catalog No. 30-2005. To make the complete growth medium, add the following components to the base medium: fetal bovine serum to a final concentration of 20%. 
  HTB-103 KATO III 人胃癌细胞
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 culture medium with floating cells to a centrifuge tube. 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. 2.. 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 10 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. 3. Add 6.0 to 8.0 ml of complete growth medium and aspirate cells by gently pipetting. 4. To remove trypsin-EDTA solution, transfer cell suspension to the centrifuge tube with the medium and cells from step #1 and spin at approximately 125 xg for 5 to10 minutes. 5. Discard supernatant and resuspend cells in fresh growth medium. Add appropriate aliquots of cell suspension to new culture vessels. 6. Place culture vessels in incubator at 37°C.
Subcultivation Ratio: A subcultivation ratio of 1:2 to 1:8 is recommended
Medium Renewal: Every 2 to 3 days
Cryopreservation
Freeze medium: Complete growth medium, 95%; DMSO, 5%
Storage temperature: liquid nitrogen vapor phase
Culture Conditions
Atmosphere: 5% CO2 in air recommended
Temperature: 37°C           HTB-103 KATO III 人胃癌细胞