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Enhanced chemiluminescence western blotting reagents

Manufactured by Thermo Fisher Scientific
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Sourced in Japan

Enhanced chemiluminescence western blotting reagents are a set of reagents designed for the detection and visualization of proteins in western blot analysis. These reagents utilize chemiluminescent technology to generate a luminescent signal that can be captured and quantified using appropriate imaging equipment.

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Lab products found in correlation

Horseradish peroxidase, by Thermo Fisher Scientific (1 mentions) Anti glyceraldehyde 3 phosphate dehydrogenase, by Merck Group (1 mentions) Anti p53 antibody, by Santa Cruz Biotechnology (1 mentions)

Close spelling variants of this product

Enhanced chemiluminescence (ECL) Western blotting reagents Enhanced Chemiluminescence (ECL) Western blotting detection reagents Western blotting chemiluminescence reagent Western blotting reagents Enhanced chemiluminescence reagent Enhanced chemiluminescence Chemiluminescence reagent

2 protocols using enhanced chemiluminescence western blotting reagents

1

Immunoblotting of NOX1 Protein

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For immunoblotting, proteins were separated by a SDS–polyacrylamide gel electrophoresis (PAGE), transferred to a nitrocellulose membrane and detected with the anti-NOX1 primary antibody (Sigma, Rehovot, Israel) and horseradish peroxidase-conjugated secondary antibody using enhanced chemiluminescence western blotting reagents (Thermo Scientific) and film (Fujifilm, Tokyo, Japan).
Sela M., Tirza G., Ravid O., Volovitz I., Solodeev I., Friedman O., Zipori D., Gur E., Krelin Y, & Shani N. (2015). NOX1-induced accumulation of reactive oxygen species in abdominal fat-derived mesenchymal stromal cells impinges on long-term proliferation. Cell Death & Disease, 6(4), e1728-.
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2

Immunoblotting with Chemiluminescence Detection

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For immunoblotting, proteins were separated by SDS–PAGE, transferred to a nitrocellulose membrane and detected with the anti-p53 antibody (Santa Cruz) or primary antibody or an anti-glyceraldehyde-3-phosphate dehydrogenase (Sigma) and horseradish peroxidase-conjugated secondary antibody using enhanced chemiluminescence western blotting reagents (Thermo Scientific) and film (Fujifilm, Tokyo, Japan). Densitometry was conducted using ImageJ software ().
Ravid O., Shoshani O., Sela M., Weinstock A., Sadan T.W., Gur E., Zipori D, & Shani N. (2014). Relative genomic stability of adipose tissue derived mesenchymal stem cells: analysis of ploidy, H19 long non-coding RNA and p53 activity. Stem Cell Research & Therapy, 5(6), 139.
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