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Hs 578Bst细胞

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  • 产品名称:Hs 578Bst细胞
  • 产品型号:Hs 578Bst
  • 产品展商:HZbscience
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  • 发布时间:2018-07-28
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简单介绍
Hs 578Bst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。Hs 578Bst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。
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Hs 578Bst细胞

器官来源: **

细胞形态: 成纤维样

ATCC Number: HTB-125™

数量: 大量

是否是肿瘤细胞: 0

物种来源: 人

运输方式: 冻存运输

生长状态: 贴壁生长

年限: 74 years

Designations: Hs 578Bst

Hs 578Bst细胞Biosafety Level: 1

Shipped: frozen

Medium & Serum: See Propagation

Growth Properties: adherent

Organism: Homo sapiens

Morphology: fibroblast


Source: Organ: mammary gland; breast

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.

Receptors: epidermal growth factor (EGF)

DNA Profile (STR): Amelogenin: X

CSF1PO: 11,13

D13S317: 11,13

D16S539: 9,12

D5S818: 11,13

D7S820: 10

THO1: 9,9.3

TPOX: 8

vWA: 17

Cytogenetic Analysis: modal number = 46; range = 42 to 48..

This is a diploid human cell line with 46,XX karyotype.Hs 578Bst细胞 Polyploidy occurred at 6.9%. Both X chromosomes were normal. The chromosome N9 pair was heteromorphic for the centromeric heterochromatin having one with the normal size and the other about twice the size of the normal.

Isoenzymes: AK-1, 1

ES-D, 1

G6PD, B

GLO-I, 1

Me-2, 0

PGM1, 1

PGM3, 1

Age: 74 years

Gender: female

Ethnicity: Caucasian

Comments: Hs 578Bst was derived by A.J. Hackett, et al. from normal breast tissue peripheral to an infiltrating ductal carcinoma which was the source for Hs 578T (see ATCC HTB-126).

Hs 578Bst may have been myoepithelial in origin since the cells possessed microfilaments and clusters of pinocytotic vesicles similar to those seen in myoepithelia in vivo.

No desmosomes were observed, estrogen receptor protein was not present, and no endogenous viruses were detected.

Note: A frozen ampule at unknown population doubling (PDL) was received at the ATCC in 1983. Cells had the potential to reach approximately 22 more population doublings before the onset of senescence. See Batch Specific information for PDL of current Distribution freeze.

Propagation: Hs 578Bst细胞ATCC complete growth medium: The base medium for this cell line is ATCC Hybri-Care Medium, Catalog No. 46-X. Hybri-Care Medium is supplied as a powder and should be reconstituted in 1 L cell-culture-grade water and supplemented with 1.5 g/L sodium bicarbonate. To make the complete growth medium, add the following components to the base medium: 30 ng/ml mouse EGF; fetal bovine serum to a final concentration of 10%.

Temperature: 37.0°C

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

Subculturing: Protocol: Remove medium, and rinse with 0.25% trypsin, 0.53 EDTA solution. Remove the solution and add an additional 1 to 2 ml of trypsin-EDTA solution. Allow the flask to sit at room temperature (or at 37C) until the cells detach. Add fresh culture medium, aspirate and dispense into new culture flasks.

Subcultivation Ratio: A subcultivation ratio of 1:3 to 1:8 is recommended

Medium Renewal: 2 to 3 times per week

Preservation: Freeze medium: Complete growth medium, 95%; DMSO, 5%

Storage temperature: liquid nitrogen vapor phase

Related Products: recommended serum:ATCC 30-2020

Recommended medium (without the additional supplements or serum described under ATCC Medium):ATCC 46-X

tumor cell line established from the same patient:ATCC HTB-126

References: 1119: Hackett AJ, et al. Two syngeneic cell lines from human breast tissue: the aneuploid mammary epithelial (Hs 578T) and the diploid myoepithelial (Hs 578Bst) cell lines. J. Natl. Cancer Inst. 58: 1795-1806, 1977. PubMed: 864756

21947: Hancock ME, et al. Method for predicting chemosensitivity of anti-cancer drugs. US Patent 4,937,182 dated Jun 26 1990

24344: Stampfer MR, et al. Hs 578Bst细胞Enhanced growth medium and method for culturing human mammary epithelial cells. US Patent 4,423,145 dated Dec 27 1983

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