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- 文献和实验
- 技术资料
- 供应商:
上海研卉生物科技有限公司
- 保存条件:
-20℃
- 英文名:
Luciferase Reporter Assay Kit
- 库存:
大量
- 规格:
200次分析
Kit Summary:
• Detection method- Luminescence
• Sample type- Cell and Tissue culture homogenates (eukaryotic cells)
• Species reactivity- Mammalian
• Application- This Luciferase Reporter Assay Kit provides a simple means for detecting luciferase activity in transfected eukaryotic cells.
Features & Benefits:
• Simple procedure; takes ~ 20-30 minutes
• Fast and convenient
• The assay ensures maximal sensitivity, consistent light output, as well as accuracy and consistency when working with multiple samples.
Kit components:
• Substrate A
• Substrate B
• Cell Lysis Buffer
Description:
Firefly luciferase has been used as a sensitive reporter for studying gene regulation and function. Luciferase provides a 1000-fold increase in sensitivity in comparison to the standard chloramphenicol acetyltransferase (CAT) assay. Firefly luciferase catalyzes the oxidative carboxylation of luciferin, a reaction with the highest efficiency of any known bioluminescence reaction. The light emission from the reaction can be recorded using a luminometer. BioVision’s Luciferase Reporter Assay Kit provides a simple means for detecting luciferase activity in transfected eukaryotic cells. For measurement of expressed luciferase in vitro, luciferase is first extracted from transfected cells through cell lysis. Then CoA, ATP, Mg²ᶧ and buffer are added to the lysate (Inclusion of CoA yields a nearly constant light emission rather than typical flash Kinetics). The luminescent reaction is then triggered by an injection of luciferin, and the emitted light is recorded by a luminometer. By providing CoA, along with ATP, Mg²ᶧ in an optimized buffer solution, BioVision’s Luciferase Reporter Assay Kit ensure maximal sensitivity, consistent light output, as well as convenience and consistency when working with multiple samples.
Storage Conditions:
-20°C
Shipping Conditions:
gel pack
USAGE: For Research Use Only! Not For Use in Humans.
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文献和实验水仙子2005 我想分别构建FOXO1 和 SIRT1基因启动子/luciferase报告质粒,用于研究X基因是否能够调控这两个启动子。但是不知道该扩增两个基因启动子区域的哪一段插入pGL3(promega)中。 另外,promega的pGL3有pGL3-basic和pGL3-enhancer,该选择哪个? 水仙子2005 继续求助 sxd5266 pGL3-basic 没有SV
在用萤火虫荧光素酶定量基因表达时 ,通常采用第二个报告基因来减少实验的变化因素。但传统的共报告基因(比如CAT,β-Gal,GUS)不够便利。因为各自的测试化学,处理要求,检测特点存在差异。Promega提供一种先进的双报告基因技术,结合了萤火虫荧光素酶测试和海洋腔肠荧光素酶测试。双荧光素酶报告基因测试系统,结合pRL载体系统,表达第二个报告基因海洋腔肠荧光素酶,在单管中进行双荧光素酶报告基因测试,快速,灵敏,简便。系统还提供PLB裂解液,用来裂解在多孔板中培养的哺乳细胞,不需操作单个样品
Luciferase 报告基因技术 自然界中广泛分布着生物发光有机体,其中包括细菌、真菌、鱼、昆虫等。 在这些生物发光有机体中催化生物发光反应的各种酶都称之为荧光素酶 (Luciferases),底物则命名为荧光素(Luciferin)。自1986― 1987 年首次被当作 报告基因使用以来,荧光素酶基因已成为目前运用最广泛的报告基因之一。尽管 来自不同物种的荧光素酶及底物存在有很大的差异,但有一个共同点,即在生物 发光反应体系中均需发生氧化反应。它通过两个步骤
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