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人子宫内膜腺癌细胞

简要描述:HTB-111 AN3 CA 人子宫内膜腺癌细胞,
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  • 产品型号:AN3 CA
  • 厂商性质:生产厂家
  • 更新时间:2021-11-11
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HTB-111 AN3 CA 人子宫内膜腺癌细胞

ATCC® Number: HTB-111™ Price: $399.00

Designations: AN3 CA

Depositors: CJ Dawe

Biosafety Level: 1

Shipped: frozen

Medium & Serum: See Propagation

Growth Proper sapiens (human)

Morphology: epties: adherent

Organism: Homoithelial

HTB-111 AN3 CA 人子宫内膜腺癌细胞

Source: Organ: uterus

Tissue: endometrium

Disease: adenocarcinoma

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 ultimay responsible for obtaining the permits. Please click here for information regarding the specific requirements for shipment to your location.


Tumorigenic: Yes

DNA Profile (STR): Amelogenin: X

CSF1PO: 12,14,15

D13S317: 12,14

D16S539: 10,14

D5S818: 11,14

D7S820: 7,10,7.1

THO1: 10,9.3

TPOX: 8,10

vWA: 14,20

Isoenzymes: AK-1, 1-2

ES-D, 1

G6PD, B

GLO-I, 2

PGM1, 1

PGM3, 1-2

Age: 55 years

Gender: female

Ethnicity: Caucasian

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%.

Atmosphere: air, 95%; carbon dioxide (CO2), 5%

Temperature: 37.0°C

Subculturing: Protocol: Volumes used in this protocol are for 75 sq. cm 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-0.53 mM EDTA solution to remove all traces of serum which contains trypsin inhibitor.

3.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 37C 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 37C.

Subcultivation Ratio: A subcultivation ratio of 1:3 to 1:6 is recommended

Medium Renewal: 2 to 3 times per week

Preservation: Freeze medium: Culture medium, 95%; DMSO, 5%

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: 22517: Dawe CJ, et al. Growth in continuous culture, and in hamsters, of cells from a neoplasma assoicated with Acanthosis nigricans. J. Natl. Cancer Inst. 33: 441-456, 1964. PubMed: 14207855

22539: Fogh J, et al. One hundred and twenty-seven cultured human tumor cell lines producing tumors in nude mice. J. Natl. Cancer Inst. 59: 221-226, 1977. PubMed: 327080

29988: Hendricks DT, et al. FHIT gene expression in human ovarian, endometrial, and cervical cancer cell lines. Cancer Res. 57: 2112-2115, 1997. PubMed: 9187105



HTB-111 AN3 CA




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