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FeQ™ ECL Substrate Kit #226

一键复制产品信息
HEK293 cell lysates were separated by SDS-PAGE and immunoblotted with anti- ACTB (β-actin) antibody. The micrograms of total cell lysates were indicated on top of the graph. Letter A, a widely used ECL from a commercial vendor; B, PiQ™ECL; and C, FeQ™ ECL.The exposure time was indicated on the right.
30 μg of lysates from HeLa (human,A)and DF-1(chicken, B) cells were separated by SDS-PAGE and immunoblotted using anti-RRM1antibody (90 kDa). Comparison of PiQ™ and FeQ™ ECLs to an ECL from vendor X showed that our products outperformed the brand of vendor X. In particular, when it comes to weak band, our ECL products were much more sensitive and powerful than Brand-X.
A total of 30 μg of cell lysates from various cell lines were separated by SDS-PAGE and immunoblotted using anti-DLAT antibody (69 kDa). The same blot was first exposed for 30 seconds (A) using an ECL reagent from vendor X for 30 seconds, washed thoroughly with TBST, then exposed for 5 seconds using our FeQ™ECL(B). Note that the existing bands in HeLa cells were greatly enhanced, and the band not detected by the vendor's ECL appeared in the pig cell line using FeQ™ ECL.
  • 基因名:
  • 货号:
    226
  • 应用:
    WB
  • 物种反应性:
规格:
50 mL,100 mL,200 mL
价格:
¥ 1,428.00,¥ 2,388.00,¥ 4,068.00
Information

Product Name: FeQ™ ECL Substrate Kit

Background:

Enhanced chemiluminescence (ECL) reagents are used with horseradish peroxidase (HRP)-conjugated secondary antibodies to detect protein abundance in Western blot. HRP catalyzes luminol oxidation in the presence of hydrogen peroxide, producing light that can be detected by X-ray film and digital imagers. FeQ™ ECL Substrate Kit is formulated with proprietary enhancers that greatly increase the intensity and duration of emitted light. FeQ™ ECL reagents are ultrasensitive and suitable to detect proteins at femtogram level. When using these reagents, the recommended dilutions for primary and secondary antibodies are 1:10,000 and 1:100,000, respectively. Compared to other commonly used ECL reagents, ours exhibit superior performance by generating extremely intense signal with low background and require ten-fold less primary and secondary antibodies.

Application Information

Allow the ECL reagents to equilibRate to room tempeRature approximately 30 min before use. Wash the membrane thoroughly to reduce non-specific signals. Mix Reagent A and B at a 1:1 Ratio. Vortex to mix. Immerse the membrane in the mixed solution for 2–3 min. Drain the excess solution using a paper towel and wrap the membrane in plastic wrap or a clear plastic folder. Detect the chemiluminescence using X-ray film or a digital imager.

Storage

Stable at 4°C for at least 1 year.

Picture
  • HEK293 cell lysates were separated by SDS-PAGE and immunoblotted with anti- ACTB (β-actin) antibody. The micrograms of total cell lysates were indicated on top of the graph. Letter A, a widely used ECL from a commercial vendor; B, PiQ™ECL; and C, FeQ™ ECL.The exposure time was indicated on the right.
  • 30 μg of lysates from HeLa (human,A)and DF-1(chicken, B) cells were separated by SDS-PAGE and immunoblotted using anti-RRM1antibody (90 kDa). Comparison of PiQ™ and FeQ™ ECLs to an ECL from vendor X showed that our products outperformed the brand of vendor X. In particular, when it comes to weak band, our ECL products were much more sensitive and powerful than Brand-X.
  • A total of 30 μg of cell lysates from various cell lines were separated by SDS-PAGE and immunoblotted using anti-DLAT antibody (69 kDa). The same blot was first exposed for 30 seconds (A) using an ECL reagent from vendor X for 30 seconds, washed thoroughly with TBST, then exposed for 5 seconds using our FeQ™ECL(B). Note that the existing bands in HeLa cells were greatly enhanced, and the band not detected by the vendor's ECL appeared in the pig cell line using FeQ™ ECL.
Citation(0)
HEK293 cell lysates were separated by SDS-PAGE and immunoblotted with anti- ACTB (β-actin) antibody. The micrograms of total cell lysates were indicated on top of the graph. Letter A, a widely used ECL from a commercial vendor; B, PiQ™ECL; and C, FeQ™ ECL.The exposure time was indicated on the right.
30 μg of lysates from HeLa (human,A)and DF-1(chicken, B) cells were separated by SDS-PAGE and immunoblotted using anti-RRM1antibody (90 kDa). Comparison of PiQ™ and FeQ™ ECLs to an ECL from vendor X showed that our products outperformed the brand of vendor X. In particular, when it comes to weak band, our ECL products were much more sensitive and powerful than Brand-X.
A total of 30 μg of cell lysates from various cell lines were separated by SDS-PAGE and immunoblotted using anti-DLAT antibody (69 kDa). The same blot was first exposed for 30 seconds (A) using an ECL reagent from vendor X for 30 seconds, washed thoroughly with TBST, then exposed for 5 seconds using our FeQ™ECL(B). Note that the existing bands in HeLa cells were greatly enhanced, and the band not detected by the vendor's ECL appeared in the pig cell line using FeQ™ ECL.
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