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</html><thumbnail_url>https://www.sopachem.com/lifesciences/wp-content/uploads/2014/01/ChIP.jpg</thumbnail_url><thumbnail_width>310</thumbnail_width><thumbnail_height>225</thumbnail_height><description>The Protein A/G magnetic particles have a specific&#xA0;surface designed for efficient Protein/DNA complex immunoprecipitation and to minimize non-specific enrichment. Proteins and other contaminants are eliminated in the washing steps. The ChIP protocol is greatly simplified by using blocked Protein A/G-coated nanoparticles. Some steps have been completely eliminated. Unlike traditional agarose beads, chromatin pre-clearing is not required. ChIP-Adembeads combined to especially designed buffers reduce background and maximize the amount of templates available for the reaction, achieving greater sensitivity where maximum DNA recovery is critical. Higher efficiency Effective IP and low non specific binding due to optimized magnetic nanoparticles ChIP-Adembeads Protein A/G after incubation with Blocking buffer have a specific surface designed for efficient Protein DNA complex immunoprecipitation and to minimize non-specific enrichment ChIP-Adembeads combined to&#xA0;Blocking Buffer&#xA0;reduce background No sedimentation problem Save time and effort Spin steps have been replaced by rapid magnetic separations, reducing the amount of hands-on time during the assay Time consuming steps are reduced or eliminated No pre-clearing step Easy to use:&#xA0;ChIP-adem-Kit contains all necessary components for successful monitoring of transcriptions factors and histones / DNA interactions Enhance sensitivity:&#xA0;method&#xA0;more effective compare to sepharose beads Ideal for many samples processing &nbsp;</description></oembed>
