Sensitive ECL Kit
Based on 8 publication(s) in Google Scholar
Sensitive ECL Kit enables low picogram detection of antigen by oxidizing luminol in the presence of HRP and peroxide. This reaction produces a prolonged chemiluminescence which can be visualized on X-ray film or digital imaging systems. The 100 mL is defined as the base specification. All larger sizes correspond to incremental volumes of this base.
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Storage :
4°C, 1 year
Protect from light
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Tel: 609-228-6898 E-mail: [email protected] [email protected]
Description & Advantages
MCE Sensitive ECL Kit enables low picogram detection of antigen by oxidizing luminol in the presence of HRP and peroxide. This reaction produces a prolonged chemiluminescence which can be visualized on X-ray film or digital imaging systems.
The Kit produces a strong, long-lived signal (6-8 hours), which, combined with very low background levels, allows for long exposure times and enables the detection of low-abundance proteins. In the Western Blot experiment, the storage solution of primary antibody (1 mg/mL) can be diluted at a ratio of 1:1,000-1:4,000 (the final concentration is about 0.25-1 μg/mL). The secondary antibody (1 mg/mL) storage solution can be diluted at a ratio of 1:5,000-1:10,000 (the final concentration is about 0.1-0.2 μg/mL).
Protocole
1. Take the High Sensitivity ECL Kit out of the refrigerator and allow it to equilibrate at room temperature for about 20 minutes.
2. Prepare the ECL working solution.
Note: Approximately 0.125 mL of High Sensitivity ECL Reagent is required per cm2 of membrane area.
a). Mix solutions A and B in a 1:1 ratio. Use a in sufficient volume to ensure that the blot is completely wetted with the ECL working solution.
b). It is recommended to prepare the working solution just before use, although the mixed reagent solution is stable for several hours at room temperature.
3. Place the blot, protein-side up, in a clean container, and add ECL working solution.
4. Incubate the blot for 3-5 minutes at room temperature.
5. Drain the excess substrate and place the blot in a plastic membrane protector. Remove all air bubbles between the blot and the surface of the membrane protector.
6. Visualize the blot using X-ray film or a CCD-based imaging system.
Publications
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Journal Impact Factor
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Most Recent
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Insect Biochem Mol Biol2026 Mar:188:104495. PMID: 41534801
Stockage
4°C, 1 year
Protect from light
Composants
| Components | HY-K2006-100 mL | HY-K2006-500 mL |
|---|---|---|
| Solution A | 50 mL | 50 mL × 5 |
| Solution B | 50 mL | 50 mL × 5 |
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