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- 详细信息
- 文献和实验
- 技术资料
- 保存条件:
-20℃保存
- 保质期:
有效期1年
- 英文名:
EGR1 luciferase reporter plasmid
- 库存:
大量
- 供应商:
翌圣生物科技(上海)股份有限公司
- 规格:
1μg
| 产品名称 |
产品编号 |
规格 |
价格(元) |
| EGR1 luciferase reporter plasmid (EGR1-Luc萤光素酶报告基因质粒) |
11529ES03 |
1 μg |
3365.00 |
产品描述
EGR1-Luc萤光素酶报告基因(报告基因质粒)(EGR1 luciferase reporter plasmid)是翌圣生物自主研发的用于检测EGR1转录活性水平为目的的报告基因。早期生长反应基因1(early growth response gene 1 , EGR1) 为早期生长反应基因家族重要成员,其蛋白产物是一个59KD的锌指样转录因子。EGR1的目的基因是分化和有丝分裂所必须的。
ERG1报告基因主要检测细胞中ERG1的活性、药物研究以及基因过表达和RNAi的表型分析等。

pEGR1-Luc是翌圣生物改造后的哺乳动物真核表达载体,在其多克隆位点插入了多个EGR1结合位点,可以高灵敏度地检测EGR1的激活水平。同时,对载体中预测出的其它转录因子以外的结合位点进行了适当的突变,增加了质粒的转录因子结合特异性。由于质粒体积减小,使得EGR1报告基因质粒更易于转染。
质粒图谱

质粒元件信息
| EGR1 response element (EGR1) |
32-71 |
| Minimal TA promoter (pTA) |
100-122 |
| Luciferase reporter gene |
154-1816 |
| SV40 late poly(A) signal |
1851-2072 |
| SV40 early promoter |
2120-2538 |
| Synthetic neomycin phosphotransferase(Neor) coding region |
2563-3357 |
| Synthetic poly(A) signal |
3382-3430 |
| Synthetic Beta-lactamase(Ampr) coding region |
4545-5405 |
| Synthetic poly(A) signal/transcriptional pause site |
5510-5663 |
运输与保存方法
冰袋运输。-20℃保存。保质期1年。
注意事项
1)本质粒未经翌圣生物允许不得用于任何商业用途,也不得移交给订货人实验室以外的任何人或单位。
2)为了您的健康,实验操作时请穿实验服和戴一次性手套。
3)本产品仅作科研用途!
使用说明
pEGR1-Luc可以采用常规转染方法转染哺乳动物细胞。用萤光素酶检测试剂盒或双萤光素酶检测试剂盒进行检测。
参考文献
[1] Stern C, Schreier B, Nolze A, et al. Knockout of vascular smooth muscle EGF receptor in a mouse model prevents obesity-induced vascular dysfunction and renal damage in vivo[J]. Diabetologia, 2020, 63(10): 2218-2234.
[2] Polovic M, Dittmar S, Hennemeier I, et al. Identification of a novel lncRNA induced by the nephrotoxin ochratoxin A and expressed in human renal tumor tissue[J]. Cellular and Molecular Life Sciences, 2018, 75(12): 2241-2256.
[3] Dussmann P, Pagel J I, Vogel S, et al. Live in vivo imaging of Egr-1 promoter activity during neonatal development, liver regeneration and wound healing[J]. BMC developmental biology, 2011, 11(1): 1-11.
[4] Fan Y, Zou W, Green L A, et al. Activation of Egr-1 expression in astrocytes by HIV-1 Tat: new insights into astrocyte-mediated Tat neurotoxicity[J]. Journal of Neuroimmune Pharmacology, 2011, 6(1): 121-129.
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文献和实验[1] Stern C, Schreier B, Nolze A, et al. Knockout of vascular smooth muscle EGF receptor in a mouse model prevents obesity-induced vascular dysfunction and renal damage in vivo[J]. Diabetologia, 2020, 63(10): 2218-2234.
[2] Polovic M, Dittmar S, Hennemeier I, et al. Identification of a novel lncRNA induced by the nephrotoxin ochratoxin A and expressed in human renal tumor tissue[J]. Cellular and Molecular Life Sciences, 2018, 75(12): 2241-2256.
[3] Dussmann P, Pagel J I, Vogel S, et al. Live in vivo imaging of Egr-1 promoter activity during neonatal development, liver regeneration and wound healing[J]. BMC developmental biology, 2011, 11(1): 1-11.
[4] Fan Y, Zou W, Green L A, et al. Activation of Egr-1 expression in astrocytes by HIV-1 Tat: new insights into astrocyte-mediated Tat neurotoxicity[J]. Journal of Neuroimmune Pharmacology, 2011, 6(1): 121-129.
Measurement of Mouse Cytomegalovirus-Induced Interferon- with Immortalized Luciferase Reporter Cells
(MCMV) infection of immortalized fibroblasts derived from mice expressing the firefly luciferase reporter downstream of the IFN-β promoter. Common methods to determine IFN-β production, including ELISA, quantitative real-time PCR (qPCR), and transient
Reporter Gene Expression for Monitoring Microorganisms in the Environment
of an organism and using it as the reporter. However, by far the commonest approach is to introduce a reporter gene into a cell to allow detection of a particular organism or to monitor its activity. The reporter gene can be located on a plasmid or to increase
pyralis和海参Renilla reniformis的luc和ruc基因是广泛应用的BL报告基因。此外,一些新的基因cDNAs也已克隆和表达。有意思的是一些新的基因,如那些能够发射红光和绿光的Phrixothrix hirtus荧光素酶,各种突变的发不同波长光的萤火虫荧光素酶。不同的荧光素酶的特性如表1。此外最近克隆和纯化的重组辣根过氧化物酶(HRP)成为一个新的生物技术工具,在不久的将来有较大的期待。实际上,高效的HRP的底物已经商业化。HRP是与CL检测组合应用最广泛的酶之一。双报告基因系统在多重
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