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LS513细胞

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  • 产品名称:LS513细胞
  • 产品型号:LS513
  • 产品展商:HZbscience
  • 产品文档:无相关文档
  • 发布时间:2018-07-07
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简单介绍
LS513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。LS513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。
产品描述

LS513细胞

器官来源: 盲肠

生长状态: 贴壁生长

运输方式: 冻存运输

年限: Dukes' type C

细胞形态: 上皮样

数量: 大量

ATCC Number: CRL-2134™

相关**: 大肠癌

是否是肿瘤细胞: 1

物种来源: 人

Designations: LS513

Depositors: L Suardet

LS513细胞Biosafety Level: 1

Shipped: frozen

Medium & Serum: See Propagation

Growth Properties: adherent

Organism: Homo sapiens

Morphology: epithelial


Source: Organ: cecum

Tumor Stage: Dukes' type C

Disease: colorectal carcinoma

Cellular Products: transforming growth factor beta 1 (TGF beta-1, 83 pg per 10 exp6 cells per 24 hours)

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. LS513细胞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

Oncogene: p53 + (wild type)

Antigen Expression: carcinoembryonic antigen (CEA); ICAM-1; HLA class I positive

DNA Profile (STR): Amelogenin: X,Y

CSF1PO: 10,13

D13S317: 9,10

D16S539: 12,13

D5S818: 9,11

D7S820: 8,11

THO1: 8

TPOX: 8

vWA: 16,17

Cytogenetic Analysis: LS513细胞Two stem lines could be distinguished. The main one was represented in 65% of the cells, with a modal number of 51,XY and 3 markers, M1 - der(1)t(1;15), M2 - der(2)t(2;3)der(3)t(2;3), M3, and a monosomy 15., The second stem line had a modal chromosome number of 52,XY and presented M2 and M3 plus an isochromosome for the long arm of chromosome 1 called M4., A trisomy 5,7, a tetrasomy 13, and a monosomy 2 and 3 were present in all of the cells analyzed; the line did not exhibit monosomy 15.

Age: 63 years

Gender: male

Ethnicity: Caucasian

Comments: LS513 is a colorectal carcinoma cell line isolated in 1985 from a primary tumor biopsy from a 63 year old Caucasian male patient diagnosed with a Dukes' C mucin secreting cecal tumor located at the Bauhin valve.

Approximately 50% of LS513 cells express surface carcinoembryonic antigen (CEA).

LS513 cells express the major histocompatibility (MHC) class I antigens HLA and beta 2 microglobulin.

MHC class II antigens (HLA-DR, DQ, and DP were not detected).

TGF beta-1 is inhibitory for proliferation of LS513 cells, whereas TGF beta-2 has no effect on the growth of these cells.

LS513 cells are 100-fold less sensitive to TGF beta-1 than the LS1034 (ATCC CRL-2158) cell line.

LS513 cells are multidrug resistant (MDR) and are tumorigenic in nude mice.

Colony forming efficiency was 30% in methylcellulose.

Propagation: ATCC complete growth medium: The base medium for this cell line is ATCC-formulated RPMI-1640 Medium, Catalog No. 30-2001. To make the complete growth medium, add the following components to the base medium: fetal bovine serum to a final concentration of 10%.

Subculturing: Subcultivation Ratio: LS513细胞A subcultivation ratio of 1:3 to 1:4 is recommended

Medium Renewal: Twice per week

Remove spent medium, add fresh 0.25% trypsin, 0.03% EDTA solution, rinse and remove trypsin.

Add fresh trypsin solution (1 to 2 ml) and let the culture sit at room temperature (or at 37C) until the cells detach.

Add fresh medium, aspirate and dispense into new flasks.

Preservation: Freeze medium: 50% Culture Medium + 40% FBS + 10% DMSO

Storage temperature: liquid nitrogen vapor phase

Doubling Time: 25 hrs

References: 23099: Suardet L, et al. Responsiveness of three newly established human colorectal cancer cell lines to transforming growth factors beta 1 and beta 2. Cancer Res. 52: 3705-3712, 1992. PubMed: 1617643

23339: Burmester JK, et al. Characterization of distinct functional domains of transforming growth factor beta. Proc. Natl. Acad. Sci. USA 90: 8628-8632, 1993. PubMed: 7690965

23418: Li CY, et al. Potential role of WAF1/Cip1/p21 as a mediator of TGF-beta cytoinhibitory effect. J. Biol. Chem. 270: 4971-4974, 1995. PubMed: 7890601

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