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- W2020200099 abstract "To procure an affinity gel capable of purifying antibody against the cytochrome P 450 component of estrogen synthetase ( P 450 ES ), we coupled purified P 450 ES to agarose supports. Our purpose was to compare two differently-activated agarose gels (Affi-Gel 15 and Tresyl-activated Sepharose) with the same P 450 ES preparation to compare the efficiency of coupling and the yield of purified antibody. Using supplier-directed protocols to covalently attach P 450 ES to each of the supports, and identical procedures to bind and elute anti- P 450 ES , we reached the following conclusions. Tresyl-activated Sepharose bound greater amounts of antigen than Affi-Gel 15 based on the amount of residual antigen after the coupling procedure and the amount of bound antigen detected by an ELISA-type method. However, both ligand-coupled supports yielded comparable amounts of purified anti- P 450 ES at a 48-fold purification relative to the starting IgG preparation." @default.
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- W2020200099 title "Estrogen synthetase (aromatase). Affinity purification of antibody against the cytochrome P450 component" @default.
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- W2020200099 doi "https://doi.org/10.1016/0022-4731(90)90220-m" @default.
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