Protein A/G/L-Sepharose is prepared by covalently coupling recombinant Protein A/G/L (Cat.# P9102-17D; containing five Ig-binding regions of protein L, five IgG binding domains from Protein A , and three Ig-binding regions of protein G. Cell wall binding regions, albumin binding regions and other non-specific binding regions have all been eliminated from the fusion protein to ensure the maximum specific IgG binding) to 6% cross-linked sepharose beads. The coupling technique is optimized to give a high binding capacity. ||The capacity of IgG binding could be greater than 10mg of human IgG per ml of wet gel.||Source: E. coli||Endotoxin: ≤0.1EU/mg||Applications:|Suitable for use in the purification of monoclonal and polyclonal antibodies and Immunoprecipitation.Other applications not tested.||Specificity: Protein A/G/L binds to all IgG subclasses from various mammalian species, including all IgGs that bind to Protein A, Protein G, and Protein L, individually. The binding capacity is greater than 10mg/ml of gel. High flow rate. Low falling off of rProtein A/G/L. pH stability 2-10.||Storage and Stability:|May be stored at 4°C. For long-term storage, aliquot and store at 4°C. Do not freeze. Aliquots are stable for at least 6 months. For maximum recovery of product, centrifuge the original vial prior to removing the cap. Further dilutions can be made in assay buffer.

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