Pierce™ Gaussia 荧光素酶闪光检测试剂盒
Pierce™ Gaussia 荧光素酶闪光检测试剂盒
Thermo Scientific™

Pierce™ Gaussia 荧光素酶闪光检测试剂盒

Thermo Scientific Pierce Gaussia 荧光素酶闪光检测试剂盒为研究人员提供了高度灵敏的测定,用于检测哺乳动物细胞培养基和全细胞裂解物中调节元素的转录活性。Gaussia荧光素酶闪光检测试剂盒的特点:•灵敏 — 提高1000倍的灵敏度允许使用较少的细胞• 具有成本效益了解更多信息
Have Questions?
更改视图buttonViewtableView
货号数量
16158100 次反应试剂盒
161591000 次反应试剂盒
货号 16158
价格(CNY)
1,153.00
Each
添加至购物车
数量:
100 次反应试剂盒
价格(CNY)
1,153.00
Each
添加至购物车
Thermo Scientific Pierce Gaussia 荧光素酶闪光检测试剂盒为研究人员提供了高度灵敏的测定,用于检测哺乳动物细胞培养基和全细胞裂解物中调节元素的转录活性。

Gaussia荧光素酶闪光检测试剂盒的特点:

灵敏 — 提高1000倍的灵敏度允许使用较少的细胞
具有成本效益 — 极灵敏的测定减少了试剂消耗
分泌荧光素酶 — 在不破坏细胞的前提下支持实时测定和动力学研究
节省时间 — 采用分泌荧光素酶进行测定只需要极少的样品处理
适合自动化 — 适合用于高通量筛选
便利 — 包含一种通用的细胞裂解缓冲液和经过优化的闪光型测定试剂
安全 — 允许用户执行非放射性测定

该闪光测定试剂盒包含的试剂用于测定哺乳动物细胞培养基和裂解物中 Gaussia 荧光素酶的活性。当与 Thermo Scientific Gaussia Luc 载体一起使用时,该试剂盒提供了一个非常灵敏的生物发光报告基因测定系统,用于对启动子或通路活性进行分泌或细胞内检测。Gaussia 荧光素酶在细胞培养基中高度分泌,可对报告基因活性进行活细胞监测。Gaussia 所产生的信号要比在类似条件下测定的萤火虫或海肾荧光素酶的信号高得多。

包括:
细胞裂解缓冲液、反应缓冲液和底物

需要:
Gaussia 荧光素酶和光度计或其他能够监测发光的仪器(如 Thermo Scientific Luminoskan Ascent 和 Varioskan 闪光微孔板读数仪)。

应用:
• 用于分析顺式调节元素和反式作用因子的启动子研究
• 药物筛选
• siRNA 和 miRNA 筛选
• 用于研究脱靶效应的多通路测定
• 分泌通路/蛋白定位报告基因测定
• 信号转导通路分析
• RNA 剪接研究

Gaussia 荧光素酶是来自海洋桡脚类动物 Gaussia princeps 的 20kDa 蛋白。生物发光酶在细胞培养基中高度分泌,可对报告基因活性进行活细胞监测。荧光素酶反应产生的光输出可与生成的 Gaussia 荧光素酶蛋白的量相关,并可用于测定驱动 Gaussia 表达的启动子的活性。Gaussia 荧光素酶所产生的信号表现出很强的闪光动力学特征,并且比在类似条件下测定的萤火虫或海肾荧光素酶的信号高得多。该检测试剂盒针对与 Gaussia Luc 载体搭配使用进行了优化,但与其他使用腔肠素作为底物的 Gaussia 荧光素酶和衍生物完全兼容。(对于辉光测定,请使用我们的 Gaussia-Dura Luc 载体。)

更多产品数据
极灵敏的多通路荧光素酶报告基因测定
难以转染的 Jurkat 细胞中的荧光素酶测定
使用多通路荧光素酶报告基因监测神经元分化
通过农药化学品激活抗氧化反应途径
多功能荧光素酶:微孔板光度计和闪光荧光素酶测定
仅供科研使用。不可用于诊断程序。
规格
检测报告基因酶、荧光素酶报告基因检测
适用细胞哺乳动物细胞
检测方法生物发光
适用于(设备)化学发光酶标仪(微孔板)
产品规格384 孔板、96 孔板
标签类型酶标记
产品线Pierce™
数量100 次反应试剂盒
底物腔肠素
底物属性化学底物
底物类型荧光素酶底物
足够用于100 次荧光素酶检测
靶标荧光素酶、Gaussia 荧光素酶
技术增强的化学发光法
类型检测试剂盒
Unit SizeEach
内容与储存
足够用于:100微孔板孔中的荧光素酶测定
• Gaussia 闪光测定缓冲液,5 mL(在 4°C 下储存)
• 100X 腔肠素,50 μL(在 -80°C 下储存)
• 荧光素酶细胞裂解缓冲液 (2X),6 mL(在室温下储存)

试剂盒可能在 -80°C 下储存或单独储存在指定温度下。

常见问题解答 (FAQ)

I got a high background signal with a Gaussia/Cypridina/Renilla Luciferase Glow/Luciferase Flash assay. What went wrong?

Here are possible causes and solutions:

- Non-specific oxidation of substrate: Use less serum in the cell culture media; Note: Albumin can increase the auto-oxidation of Vargulin; Avoid repeated freezing and thawing of the sample.
- Control sample is contaminated: Use new sample; Change pipette tips after each well.

Find additional tips, troubleshooting help, and resources within our Protein Assays and Analysis Support Center.

I am getting a high saturating signal with a Gaussia/Cypridina/Renilla Luciferase Glow/Luciferase Flash assay. What could have happened?

This could be due to high luciferase expression. Here are some suggestions:

  • Reduce incubation time before collecting samples. 
  • Decrease the integration time on the instrument.
  • Dilute the sample: for secreted Gaussia/Cypridina Luciferase, dilute the sample using media from the cell culture; for cell lysate, dilute the sample using lysis buffer 


  • Note: A low sample volume can increase assay variability. Dilute the sample and use the recommended volume of 10-20 µL per assay.

    Find additional tips, troubleshooting help, and resources within our Protein Assays and Analysis Support Center.

    Why am I getting a low signal in lysate using a Gaussia/Cypridina/Renilla Luciferase Glow/Luciferase Flash assay? Can you provide some suggestions?

    Here are possible causes and solutions:

    - Non-optimized lysis buffer used: Assay luciferase activity in the media to confirm good expression of luciferase; Use only the provided lysis buffer.
    - Low luciferase expression: Lyse cells in smaller volume of 1X Cell Lysis Buffer; Use a different promoter or growth conditions to improve expression; Increase the integration time on the instrument; Scale up volume of sample and reagent per well.

    Find additional tips, troubleshooting help, and resources within our Protein Assays and Analysis Support Center.

    I got a low signal in media when I used a Gaussia/Cypridina/Renilla Luciferase Glow/Luciferase Flash assay. What happened?

    Here are possible causes and solutions:

    - Insufficient luciferase accumulation in media: Incubate cells for a longer time.
    - Low luciferase expression: Use less media per well during the experiment;.Use a different promoter or growth conditions to improve expression;.Increase the integration time on the instrument;.Scale-up the volume of sample and reagent per well.
    - Treatment interfered with cellular secretory pathway: Transfect cells with a plasmid for constitutive expression of Luciferase (i.e., with pTK or pCMV promoter); Determine if luciferase actively expresses in media without treatment. Add treatment; Determine if there is a corresponding drop in luciferase activity from the constitutively expressed plasmid.

    Find additional tips, troubleshooting help, and resources within our Protein Assays and Analysis Support Center.

    I am getting no signal with my Gaussia/Cypridina/Renilla Luciferase Glow/Luciferase Flash assay. Why is this?

    Here are possible causes and solutions:

    - Low transfection efficiency: Optimize transfection conditions using a visual transfection control (e.g., a plasmid over-expressing a fluorescent protein); Verify plasmid DNA quality - use only transfection grade DNA; Use actively dividing, low passage cells; Use a different cell type.
    - No or low promoter activity: Use conditions known for promoter activation; Incubate cells for a longer time; Change growth conditions to improve expression; Use a different promoter.
    - Substrate auto-oxidized: Protect substrate from light and air; Maintain 100X Coelenterazine at -80 degrees C; maintain 100X Vargulin at -80 degrees C; Prepare new Coelenterazine Working Solution if used longer than 8 hours; Prepare new Vargulin Working Solution if used longer than 2 hours

    Find additional tips, troubleshooting help, and resources within our Protein Assays and Analysis Support Center.