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- 详细信息
- 询价记录
- 文献和实验
- 技术资料
- 生长状态:
贴壁生长
- 细胞形态:
内皮样
- 库存:
大量
- 运输方式:
冻存运输
- 物种来源:
人
- 是否是肿瘤细胞:
0
- 组织来源:
somatic cell hybrid
- ATCC Number:
CRL-2922™
| Designations: | EA.hy926 | ||
| Depositors: | CS Edgell | ||
| Biosafety Level: | 1 | ||
| Shipped: | frozen | ||
| Medium & Serum: | See Propagation | ||
| Growth Properties: | adherent | ||
| Organism: | Homo sapiens | ||
| Morphology: | endothelial |
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| Source: | Tissue: somatic cell hybrid | ||
| 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. | ||
| Antigen Expression: | Factor VIII-related antigen; Homo sapiens, expressed | ||
| DNA Profile (STR): | Amelogenin: X CSF1PO: 10,11,12 D13S317: 11 D16S539: 11,12 D5S818: 11 D7S820: 8,9,10 THO1: 6,8,9.3 TPOX: 8,9 vWA: 14,17 |
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| Comments: | The human umbilical vein cell line, EA.hy926, was established by fusing primary human umbilical vein cells with a thioguanine-resistant clone of A549 by exposure to polyethylene glycol (PEG). Hybrid clones were selected in HAT medium and screened for factor VIII-related antigen. EA.hy926 cells have been maintained for more than 100 population doublings (PDLs). Electron photomicrographs demonstrate cytoplasmic distribution of Weibel-Palade bodies and tissue-specific organelles, characteristics of differentiated endothelial cell functions such as angiogenesis, homeostasis/thrombosis, blood pressure and inflammation. [PubMed: 6407019] [PubMed: 2079463] | ||
| 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%. Atmosphere: air, 95%; carbon dioxide (CO2), 5% Temperature: 37.0°C |
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| Subculturing: | Protocol: Volumes used in this protocol are for 75 sq cm flasks; proportionally reduce or increase amount of dissociation medium for culture vessels of other sizes.
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| Preservation: | Freeze medium: Complete Growth medium, 95%; DMSO, 5% Storage temperature: liquid nitrogen vapor phase |
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| Related Products: | Recommended medium (without the additional supplements or serum described under ATCC Medium):ATCC 30-2002 recommended serum:ATCC 30-2020 0.25% (w/v) Trypsin - 0.53 mM EDTA in Hank' BSS (w/o Ca++, Mg++):ATCC 30-2101 phosphate-buffered saline:ATCC 30-2200 Cell culture tested DMSO:ATCC 4-X Erythrosin B vital stain solution:ATCC 30-2404 Trypan Blue vital stain solution:ATCC 30-2402 |
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| References: | 92902: Edgell CJ, et al. Permanent cell line expressing human factor VIII-related antigen established by hybridization. Proc. Natl. Acad. Sci. USA 80: 3734-3737, 1983. PubMed: 6407019 92903: Bauer J, et al. In vitro model of angiogenesis using a human endothelium-derived permanent cell line: contributions of induced gene expression, G-proteins, and integrins. J. Cell. Physiol. 153: 437-449, 1992. PubMed: 1280276 92904: Edgell CJ, et al. Endothelium specific Weibel-Palade bodies in a continuous human cell line, EA.hy926. In Vitro Cell. Dev. Biol. 26: 1167-1172, 1990. PubMed: 2079463 92905: Rieber AJ, et al. Extent of differentiated gene expression in the human endothelium-derived EA.hy926 cell line. Thromb. Haemostasis 69: 476-480, 1993. PubMed: 8322270 |
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- 作者
- 内容
- 询问日期
文献和实验ESCO-1520 ESCO 温度探头EA701CA-4 EA701CA-4
ESCO-1526 ESCO 刷子EA109E-1 刷子EA109E-1 ESCO-1525 ESCO 夹具EA500-100 夹具EA500-100 ESCO-1524 ESCO 超音厚度计EA706X-10 EA706X-10 ESCO-1523 ESCO 扳手EA614CE-13 EA614CE-13 ESCO-1522 ESCO 扳手EA616BB-13 EA616BB-13 ESCO-1521 ESCO 翘片修正器EA
ESCO-2185 ESCO 特殊扎带EA475HB-2 EA475HB-2
ESCO-20130001 ESCO 插座EA940CH-2 EA940CH-2 CP-1310090072 ESCO 胶锤EA575D-25 EA575D-25 CP-1310090071 ESCO 胶锤EA575VH-60 EA575VH-60 ESCO-1310 ESCC 加长改锥EA550AK EA550AK ESCO-10041 ESCO 丝维套装EA829B EA829B ESCO-10040 ESCO 板手EA613
相关专题 原理 B淋巴细胞有表面Fc受体,以鸡红细胞作为指示细胞与相应的抗红细胞抗体形成EA,B淋巴细胞可以通过Fc受体与EA形成花环,以此计算B淋巴细胞的数目。Fc受体并非B细胞所特有,中性粒细胞、单核细胞及巨噬细胞表面均有这种受体,但这些细胞可以通过形态学加以区别。此方法简单,目前较常采用,以检测B淋巴细胞的百分率。 材料与试剂 基本同EAC花环试验,只是不需要补体。 操作方法 1.EA悬液的制备 取4%鸡红细胞
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