PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 18234205-5 2008 We identified two characteristic binding sites of lysozyme on SP Sepharose Fast Flow and one multipoint interaction of lysozyme with SP Sepharose XL. Sepharose 65-74 lysozyme Homo sapiens 50-58 19739025-2 2009 Lysozyme and ovalbumin were separated with Q Sepharose Fast Flow anion exchange chromatography in the first step, resulting in two peaks of lysozyme and three peaks of ovalbumin with 87% and 70% purity by HPLC, respectively. Sepharose 45-54 lysozyme Homo sapiens 0-8 18289663-3 2008 Net-positively-charged Lys (pI=11) and net-negatively-charged HSA (pI=5.5) adsorb so strongly to sulfopropyl sepharose (SP; a negatively-charged, strong cation-exchange resin, -0.22 mmol/mL exchange capacity) that both resist displacement by net-neutral IgG (pI=7.0) in simultaneous adsorption competition experiments. Sepharose 120-122 lysozyme Homo sapiens 23-26 16038296-1 2005 This work provides a theoretical analysis of multicomponent adsorption kinetics for conditions typical of protein adsorption in porous ion exchangers as well as experimental results for the adsorption of lysozyme/cytochrome c mixtures in the cation exchanger SP-Sepharose-FF. Sepharose 262-271 lysozyme Homo sapiens 204-212 11217018-3 2001 The fraction with an average VI content of 8.5% was most efficient as a reusable displacer for IMAC of ovalbumin, lysozyme and other proteins of egg white on Cu2+-IDA-Sepharose. Sepharose 167-176 lysozyme Homo sapiens 114-122 33973097-3 2021 The objective of this work was to test the functionality of the strategy of Rational Design of Immobilized Derivatives for the immobilization by electrostatic adsorption of egg white lysozyme on SP-Sepharose FastFlow support. Sepharose 198-207 lysozyme Homo sapiens 183-191 33973097-7 2021 The enzymatic activity assay with the chitosan substrate showed the catalytic functionality of the lysozyme-SP-Sepharose immobilized derivative (35.85 +- 3.07 U/support g), which preserved 78% functional activity. Sepharose 111-120 lysozyme Homo sapiens 99-107 35350183-0 2022 Investigation of Lysozyme Diffusion in Agarose Hydrogels Employing a Microfluidics-Based UV Imaging Approach. Sepharose 39-46 lysozyme Homo sapiens 17-25 35350183-8 2022 The estimated diffusion coefficients for lysozyme were between 0.80 +- 0.04x10-10 m2 s-1 for 1.5% (w/w) low-melt agarose and 1.14 +- 0.02x10-10 m2 s-1 for 0.5% (w/w) unmodified agarose. Sepharose 113-120 lysozyme Homo sapiens 41-49 35350183-8 2022 The estimated diffusion coefficients for lysozyme were between 0.80 +- 0.04x10-10 m2 s-1 for 1.5% (w/w) low-melt agarose and 1.14 +- 0.02x10-10 m2 s-1 for 0.5% (w/w) unmodified agarose. Sepharose 177-184 lysozyme Homo sapiens 41-49 6430120-1 1984 Human milk lysozyme was purified by heparin-Sepharose affinity chromatography and Sepharose 4B gel-permeation chromatography. Sepharose 44-53 lysozyme Homo sapiens 11-19 6430120-1 1984 Human milk lysozyme was purified by heparin-Sepharose affinity chromatography and Sepharose 4B gel-permeation chromatography. Sepharose 82-94 lysozyme Homo sapiens 11-19 566118-2 1978 It was that gel filtration chromatography on agarose columns can be used selectively to purify lysozyme, due to the fact that this protein interacts with the agarose matrix and elutes later than the corresponding total volume for the column. Sepharose 45-52 lysozyme Homo sapiens 95-103 566118-2 1978 It was that gel filtration chromatography on agarose columns can be used selectively to purify lysozyme, due to the fact that this protein interacts with the agarose matrix and elutes later than the corresponding total volume for the column. Sepharose 158-165 lysozyme Homo sapiens 95-103 1000849-0 1976 Effect of agarose variability on the measurement of lysozyme activity. Sepharose 10-17 lysozyme Homo sapiens 52-60 1000849-1 1976 Lysozyme assays are often performed by a diffusion technique utilizing agarose gels impregnated with substrate organisms (lysoplates), but the results differ greatly from those obtained with spectrophotometric or immunologic techniques. Sepharose 71-78 lysozyme Homo sapiens 0-8 1000849-4 1976 The different agaroses had variable effects on determinations of normal serum lysozyme, and the results obtained on any given gel agreed with neither those found on other gels nor with independent assay in another system. Sepharose 14-22 lysozyme Homo sapiens 78-86 29652825-5 2018 Subsequently, the lysozyme loaded sericin/agarose composite gel was successfully prepared by the solution impregnation method. Sepharose 42-49 lysozyme Homo sapiens 18-26 14577450-7 2003 The numerical results show that gellified lysozyme (crystals "locked"on the matrix of agarose gel) precipitates to produce "spaced deposits". Sepharose 86-93 lysozyme Homo sapiens 42-50 711708-1 1978 For the isolation of human lysozyme from the urine of leukemia patients, a simple method has been established which involves precipitation of urinary proteins by 60% saturation with ammonium sulfate, fractionation of crude lysozyme on Sephadex G-50 and purification by CM-Sepharose chromatography. Sepharose 272-281 lysozyme Homo sapiens 27-35 191025-0 1977 Lysozyme-agarose interaction. Sepharose 9-16 lysozyme Homo sapiens 0-8 265197-0 1977 Electrophoresis of lysozyme into Microscoccus-containing agarose gel: quantitative and analytical applications. Sepharose 57-64 lysozyme Homo sapiens 19-27 265197-1 1977 Electrophoresis of lysozyme into agarose gel containing Micrococcus lysodeikticus causes lysis of the microorganism, allowing the development of two methods, one for quantitation ("lyso-rocket electrophoresis") and the other for electrophoretic characterization ("crossed lyso-electrophoresis") of lysozyme. Sepharose 33-40 lysozyme Homo sapiens 19-27 29652825-9 2018 So, the lysozyme loaded sericin/agarose gel is a potential alternative biomaterial for wound dressing. Sepharose 32-39 lysozyme Homo sapiens 8-16