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ECL化学发光底物

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  • ¥575 - 1975
  • pierce
  • 2025年12月23日
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    • 详细信息
    • 询价记录
    • 文献和实验
    • 技术资料
    • 库存

      大量现货

    • 保存条件

      4℃

    • 英文名

      ECL Western Blotting Substrate

    • 供应商

      上海伟进生物

    • 规格

      50ML/500ML

    规格:产品价格:¥575
    规格:50ML产品价格:¥575
    规格:500ML产品价格:¥1975
    Thermo Scientific Pierce ECL Western Blotting Substrate is a value-priced, entry-level peroxidase substrate for enhanced chemiluminescence (ECL) that directly replaces costlier products without the need to re-optimize conditions.
    Pierce ECL Western Blotting Substrate provides reliability and performance equivalent to other standard enhanced chemilumescent (ECL) substrates for detection of horseradish peroxidase (HRP) enzyme activity. Yet, Pierce ECL Substrate costs much less. Because the luminol and peroxide reagent-formulations are identical to other commercially available substrate products, one can switch to Pierce ECL without needing to optimize probing conditions or incubation protocols. Simply switch to Pierce ECL and save a bundle.
    Highlights:
    ECL substrate – an enhanced chemiluminescent substrate for detection of horseradish peroxidase (HRP) activity from antibodies and other Western blot probes
    About half the cost of other ECL Substrates – low overhead and a commitment to customer value enables Thermo Fisher Scientific to make this product available to you at a significantly lower price than other companies (these claims are based on the 2010 U.S. list prices)
    No optimization required – switching to Pierce ECL substrate from other entry-level ECL substrates does not require optimization or protocol changes
    A name you can can rely on – count on the strong quality assurance, technical support and reputation behind Thermo Scientific Pierce Protein Research Products
    Product Details:
    Pierce ECL Western Blotting Substrate provides performance identical to the original Amersham ECL Western Blotting Detection Reagent from GE Healthcare, but it costs much less. If you are currently using a needlessly expensive entry-level ECL substrate, you can switch to Pierce ECL Western Blotting Substrate without any optimization. Because these products are identical, they perform the same.

    Signal intensity of Thermo Scientific Pierce ECL Western Blotting Substrate is comparable to GE Healthcare ECL Substrate. HeLa cell lysate was separated by SDS-PAGE and transferred to nitrocellulose membrane to detect β-actin. The signal was detected and analyzed using the Kodak 1D Imaging Station. Error bars represent ±20% difference in relative intensity units.


    Thermo Scientific Pierce ECL Western Blotting Substrate for detection of proteins on nitrocellulose or PVDF. β-actin and β-galactosidase protein in HeLa cell and E. coli lysates were detected by Western blotting. The membranes were blocked with 5% skim milk and probed with primary antibody at 1µg/mL. The membranes were washed and then incubated with 0.2µg/mL of HRP-conjugated goat anti-mouse IgG (Part No. 31430) and then washed again. Working solutions of the Pierce ECL Substrate and GE Healthcare ECL Reagent were prepared according to the manufacturers’ instructions and added to replicate membranes for 1 minute. The membranes were removed from the substrates and placed in plastic sheet protectors and exposed to Thermo Scientific CL-XPosure Film (Part No. 34090) and developed.

    Pierce ECL Substrate Western blot detection of recombinant protein. Dilutions of recombinant bovine TNF-a (Thermo Scientific) were prepared, electrophoresed and transferred to nitrocellulose membranes (Part No. 88025). The membranes were blocked with 5% skim milk and probed with 4µg/mL of rabbit anti-bovine TNF-a (Thermo Scientific). The membranes were washed and then incubated with 0.4µg/mL of HRP-conjugated goat anti-rabbit IgG (Part No. 31460) and then washed again. Working solutions of the substrates were prepared according to the manufacturers’ instructions and added to the membranes for 1 minute. The membranes were removed from the substrates and placed in plastic sheet protectors. Each membrane was exposed to Hyperfilm* Film (GE Healthcare).








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    相关实验
    • 化学发光底物

      反应迅速,在1~5s内即可完成;具有背景低、信比高的优点,其检测极限可达5×10-9mol,发光量与AE浓度呈良好的线性反应,是一类的标记物。 3.电化学发光(electrochemiluminescence,ECL)反应在电极表面进行。发光底物为三联吡啶钌[Ru(bpy) 3 2+],另一反应物为三丙胺(TPA)。在阳电极表面,以上两化学物质可同时失去电子发生氧化反应。二价的Ru(bpy) 3 2+ 被氧化成三价Ru(bpy) 3

    • 化学发光底物

      酯(acridiniumester,AE)类类发光剂不需催化剂的存在,在有过氧化氢的稀碱溶液中即能发光。反应式如下: 电化学发光原理 上式反应迅速,在1~5s内即可完成;具有背景低、信比高的优点,其检测极限可达5×10 -9 mol,发光量与AE浓度呈良好的线性反应,是一类的标记物。 3、电化学发光(electrochemiluminescence,ECL)反应在电极表面进行。发光底物为三联吡啶钌[Ru(bpy)32+],另一反应物为三丙胺(TPA)。在阳

    • 增强化学发光法(ECL)

      Ecl 显色原理:鲁米诺在免疫测定中既可用作标记物,也可用作过氧化物酶的底物。在Ecl底物中,含有H2O2和鲁米诺,在HRP(辣根过氧化物酶)的作用下,发出荧光来。 试验步骤: 1)将两种显色底物1:1等体积混合(一般各1ml/membrane)。 2)将混合物覆盖在膜表面,1-2分钟,摇晃使均匀。 3)用保鲜膜把膜包起来,放入夹板中。 4)在暗室中将X光片,覆盖在膜的上面,夹好夹子,曝光1min。 5)显影、定影。 6)根据结果调整曝光时间和曝光区域,得到

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    ¥575 - 1975