The immunodetection phase of Western blotting, consisting of blocking, antibody incubations, and washing steps, may be subject to experimental variability. The SNAP i.d. 2.0 system both accelerates immunodetection, shortening time to results, and enables parallel processing of blots, making it easy to apply consistent conditions across experiments.
The SNAP i.d. 2.0 system uses a vacuum manifold to drive blocking reagents, antibodies, and wash buffers directly through the PVDF or nitrocellulose membrane of the blot. As a result, immunodetection is much faster: a process requiring 4-24 hours using traditional, platform shaker-dependent Western blot processing takes only 30 minutes.
Watch Video: How the vacuum-driven SNAP i.d. 2.0 System enables 30-minute immunodetection of Western blots.
The SNAP i.d. 2.0 Protein Detection System is intended for research use only. It is not for use in diagnostic procedures.
The system consists of the following components:
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