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bEnd.3细胞

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  • 产品名称:bEnd.3细胞
  • 产品型号:bEnd.3
  • 产品展商:HZbscience
  • 产品文档:无相关文档
  • 发布时间:2018-09-19
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简单介绍
bEnd.3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。bEnd.3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

bEnd.3细胞

组织来源: cerebral cortex

相关**: 其他**

ATCC Number: CRL-2299™

品系: BALB/c

生长状态: 贴壁生长

物种来源: 小鼠

是否是肿瘤细胞: 0

细胞形态: 内皮样

细胞类型: 其他细胞类型

运输方式: 冻存运输

年限: 6 weeks

器官来源: 大脑

数量: 大量

Designations: bEnd.3

Depositors: EC Butcher

bEnd.3细胞Biosafety Level: 1

Shipped: frozen

Medium & Serum: See Propagation

Growth Properties: adherent

Organism: Mus musculus

Morphology: endothelial


Source: Organ: brain

Strain: BALB/c

Tissue: cerebral cortex

Disease: endothelioma

Cell Type: endothelialpolyoma middle T antigen transformed

Cellular Products: von Willebrand factor

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.

Restrictions: bEnd.3细胞The bEnd.3 cell line is provided for research use only under the following terms:1. bEnd.3 cells, or products derived from them, must not be sold or used for commercial purposes. Nor can the cells be distributed to third parties for purpose of sale, or producing for sale, bEnd.3 cells or their products. Commercial interests are the exclusive property of The Max Planck Society. 2. Any proposed commercial use of bEnd.3 cells, or products derived from them, must first be negotiated with Dr. Britta Engelhardt, on behalf of the late Dr. Werner Risau, Max-Planck-Institut fur physiologische und klinische Forschung, W.G. Kerckoff Institut, Abteilung molekulare Zellbiologie, Parkstrasse 1, 61231 Bad Nauheim, Germany. Telephone: 49-6032-705203/265; FAX: 49-6032-072259; email: b.engelhardt@kerckoff.mpg.de3. In all papers reporting any use of bEnd.3 cells, or products derived from them, a direct reference will be made to the original publication (Montesano, et al. Cell 62:435-445, 1990).

Antigen Expression: ICAM-1 +; VCAM-1 +; MAdCAM-1 +

Age: 6 weeks

Comments: The cells were transformed by infection with the NTKmT retrovirus vector that expresses polyomavirus middle T antigen. [39039]

The endothelial nature of these cells was confirmed by the observed expression of von Willebrand factor and uptake of fluorescently labeled low density lipoprotein (LDL). [39039]

The expression of Peyer's Patch high endothelial receptor for lymphocytes, the mucosal vascular addressin (MAdCAM-1) and E-selectin can be induced on bEnd.3 cells by cytokines and lipopolysaccharide (LPS). [39040]

This induction by Tumor Necrosis Factor alpha (TNF alpha), interleukin 1 (IL-1) or LPS is concentration and time dependent. [39040]

MAdCAM-1 is expressed on the surface of unstimulated bEnd.3 cells at early passages but not at passages greater than 30.

Intracellular adhesion molecule 1 (ICAM-1) is constitutively expressed on the cells, and expression is increased by treatment with LPS, IL-1 and TNF alpha.bEnd.3细胞 [39040]

Vascular cell adhesion molecule 1 (VCAM-1) is constitutively expressed on the cells at early passages but not at passages over 30.

P-selectin can be induced on bEnd.3 cells by Tumor Necrosis Factor alpha (TNF alpha) at both early and late passages but expression is greater at passages over 30.

Propagation: ATCC complete growth medium: The base medium for this cell line is ATCC-formulated Dulbecco's Modified Eagle's Medium, Catalog No. 30-2002. To make the complete growth medium, add the following components to the base medium: fetal bovine serum to a final concentration of 10%.

Temperature: 37.0°C

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

Subculturing: Protocol: Remove and discard culture medium. Briefly rinse the cell layer with 0.25% (w/v) Trypsin-0.03% (w/v) EDTA solution to remove all traces of serum which contains trypsin inhibitor.Add 1.0 to 2.0 ml of Trypsin-EDTA solution to flask and observe cells under an inverted microscope until cell layer just begins to detach. Add 6.0 to 8.0 ml of complete growth medium and aspirate cells by gently pipetting. Add appropriate aliquots of the cell suspension to new culture vessels.

Subcultivation Ratio: A subcultivation ratio of 1:6 to 1:10 is recommended

Medium Renewal: Every 2 to 3 days

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

Storage temperature: liquid nitrogen vapor temperature

Related Products: Recommended medium (without the additional supplements or serum described under ATCC Medium):ATCC 30-2002

recommended serum:ATCC 30-2020

References: 39039: Montesano R, et al. Increased proteolytic activity is responsible for the aberrant morphogenetic behavior of endothelial cells expressing the middle T oncogene. bEnd.3细胞Cell 62: 435-445, 1990. PubMed: 2379237

39040: Sikorski EE, et al. The Peyer's patch high endothelial receptor for lymphocytes, the mucosal vascular addressin, is induced on a murine endothelial cell line by tumor necrosis factor-alpha and IL-1. J. Immunol. 151: 5239-5250, 1993. PubMed: 7693807

39041: Williams RL, et al. Embryonic lethalities and endothelial tumors in chimeric mice expressing polyoma virus middle T oncogene. Cell 52: 121-131, 1988. PubMed: 3345558

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