ROTI ® Garose-Biotin and Streptavidin beads offer the perfect solution for the isolation of biotinylated and streptavidinated molecules in benchtop column chromatography or in batch procedures. Rapid, mild and highly specific purification Suitable for isolation of DNA, proteins and other molecules of all sizes High binding capacity High recovery rates With a value of K a ~10 -14 /M, the affinity of avidin and streptavidin for biotin is the strongest non-covalent bond between molecules known in biochemistry. Efficient and highly specific isolation of biotinylatd or avidin/streptavidin-tagged molecules via affinity chromatography is based on this particular affinity. Directions for use The matrix is easy to pack and results in very evenly packed columns. Elution is carried out via 8 M guanidine-HCl or prior to gel loading during heating in gel loading buffer. Merely no unspecific binding of unlabelled molecules takes place, even during purification from raw extracts. ROTI ® Garose-Biotin Beads ROTI ® Garose for biochemistry Biotin coupled agarose beads for affinity chromatography. 50 % bead suspension in water stabilised with 0,02 % sodium azide. One-step isolation of avidin/streptavidin-tagged molecules from total lysates For batch mode and gravity flow Suitable for Recommended for isolation of avidin- or streptavidin labelled molecules in batch mode or via columns via low pressure affinity chromatography. Directions for use The matrix of ROTI ® Garose-Biotin Beads consists of beaded 4 % cross-linked agarose. Biotin is immobilised to the beads through a spacer arm and covalent carboxy/amide linkage, not only minimizing biotin leakage during elution, but also enhancing the binding capacity by reduction of steric effects. Merely no unspecific binding of unlabelled molecules takes place, even during purification from raw extracts.