Description
- Most sensitive of Advansta’s HRP substrates, for low-abundance proteins
- Long-lasting signal for flexible imaging
- Low background for high signal-to-noise
- Image by CCD or film
Description

WesternBright Sirius HRP substrate
WesternBright® Sirius® is the most sensitive HRP substrate available from Advansta for chemiluminescent Western blotting. With attomole sensitivity and a long-lasting signal, WesternBright Sirius allows you to detect bands not visualized with other substrates. High signal-to-noise and a large dynamic range make it ideal for quantifying low-intensity bands.
WesternBright Sirius is the most sensitive of the HRP substrates
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WesternBright Sirius is designed for sensitive detection and low antibody concentrations. With low background and a strong, long-lasting chemiluminscent signal, WesternBright Sirius is the best choice for quantifying low-abundance bands.
WesternBright Sirius provides a strong chemiluminscent signal
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WesternBright Sirius is the most sensitive chemiluminescent HRP substrate offered by Advansta, specially engineered to produce an extremely strong signal to detect low-abundance proteins and to work with very low antibody concentrations.
High sensitivity, low background

Sensitivity of chemiluminescent substrates from various suppliers. 2-fold serial dilutions of purified transferrin were electrophoresed by SDS-PAGE then transferred to a PVDF membrane. The blots were blocked then probed with a rabbit anti-transferrin primary antibody followed by an HRP- conjugated anti-rabbit secondary antibody. Various substrates were applied to the membranes then signal was measured with a CCD camera.
Image blots hours after substrate incubation
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A slot blot containing a serial dilution of an HRP-conjugated antibody was incubated with WesternBright Sirius, and imaged at the times indicated. After 8 hours, the bands are still easily detected with a 2 minute exposure.
Low background for sensitive detection and better quantitation
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WesternBright Sirius provides sensitive detection combined with extremely low background. Duplicate Western blots were performed with samples of plasma, diluted either 1:100 (left lanes) or 1:600 (right lanes) in PBS, and probed with a goat antisera primary antibody and an HRP-conjugated secondary antibody. After detection with either WesternBright Sirius or SuperSignal® West Femto (Thermo Scientific), the blots were imaged for 8.3 minutes. The signal-to-noise ratio is shown for each band.





