PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 20052520-2 2010 Adsorption of bovine serum albumin (BSA) and lysozyme (LSZ) on the composite material was observed in 2 and 10 mol m(-3) phosphate buffer solutions. Phosphates 121-130 lysozyme Homo sapiens 21-53 21940222-4 2011 High desorption of lysozyme from Fe(3)O(4) (PEG+CM-CTS) NPs were achieved using phosphate buffer solution (PBS) (20 mM, pH 5.0, 0.2 M NaCl), PBS (20 mM, pH 5.0, 0.5 M NaCl) and acetic acid (0.2 M, pH 4.0) as eluents. Phosphates 80-89 lysozyme Homo sapiens 19-27 20824660-5 2010 trypsin, ribonuclease A, lysozyme and cytochrome c) was successfully achieved at pH 3.5 of 10 mmol/L phosphate buffer. Phosphates 102-111 lysozyme Homo sapiens 25-33 19856993-2 2009 We examined the enthalpy changes accompanying the binding of met-hemoglobin, met-myoglobin, and lysozyme to layered alpha-Zr(IV)phosphate (20 mM NaPipes, 1 mM TBA, pH 7.2, 298 K) by titration calorimetry, under specific conditions. Phosphates 128-137 lysozyme Homo sapiens 96-104 15881359-6 2005 Ovalbumin and lysozyme were successfully purified to homogeneity and ovaltransferrin to ca 60% purity from the hen egg white sample with yields over 90% in 15.0% PEG1000-17.0% phosphate ATPs at pH 9.2 with the apparatus rotating at 850 r/min and mobile phase flow rate of 1.0 mL/min. Phosphates 176-185 lysozyme Homo sapiens 14-22 17633207-3 2007 Moreover, the non-covalent complexes of lysozyme with the four new genistein phosphates were detected by ESI-MS. Phosphates 77-87 lysozyme Homo sapiens 40-48 26049224-2 2008 The inactivation of lysozyme in phosphate buffer was a function of electric field strength, treatment time, electrical conductivity, and enzyme concentration. Phosphates 32-41 lysozyme Homo sapiens 20-28 9268541-6 1997 In particular, the permeability coefficient of phosphate through the lysozyme-adsorbed membrane increased to twice that of the nonadsorbed membrane. Phosphates 47-56 lysozyme Homo sapiens 69-77 15648573-4 2004 It was shown that the amount of complexed lysozyme reached to 1.7 g/g dry gel, when high content of a phosphate-carrying monomer with 5 ethylene glycol units was incorporated into a hydrogel. Phosphates 102-111 lysozyme Homo sapiens 42-50 15648573-5 2004 It was further found that lysozyme complexed with phosphate-carrying network could be released by immersion of the lysozyme/hydrogel composite in a phosphate buffer solution of pH 7.4 owing to the pH-sensitivity of the hydorgel but no lysozyme was released at pH 1.4. Phosphates 50-59 lysozyme Homo sapiens 26-34 15648573-5 2004 It was further found that lysozyme complexed with phosphate-carrying network could be released by immersion of the lysozyme/hydrogel composite in a phosphate buffer solution of pH 7.4 owing to the pH-sensitivity of the hydorgel but no lysozyme was released at pH 1.4. Phosphates 50-59 lysozyme Homo sapiens 115-123 15648573-5 2004 It was further found that lysozyme complexed with phosphate-carrying network could be released by immersion of the lysozyme/hydrogel composite in a phosphate buffer solution of pH 7.4 owing to the pH-sensitivity of the hydorgel but no lysozyme was released at pH 1.4. Phosphates 50-59 lysozyme Homo sapiens 115-123 15648573-5 2004 It was further found that lysozyme complexed with phosphate-carrying network could be released by immersion of the lysozyme/hydrogel composite in a phosphate buffer solution of pH 7.4 owing to the pH-sensitivity of the hydorgel but no lysozyme was released at pH 1.4. Phosphates 148-157 lysozyme Homo sapiens 26-34 15648573-5 2004 It was further found that lysozyme complexed with phosphate-carrying network could be released by immersion of the lysozyme/hydrogel composite in a phosphate buffer solution of pH 7.4 owing to the pH-sensitivity of the hydorgel but no lysozyme was released at pH 1.4. Phosphates 148-157 lysozyme Homo sapiens 115-123 15648573-5 2004 It was further found that lysozyme complexed with phosphate-carrying network could be released by immersion of the lysozyme/hydrogel composite in a phosphate buffer solution of pH 7.4 owing to the pH-sensitivity of the hydorgel but no lysozyme was released at pH 1.4. Phosphates 148-157 lysozyme Homo sapiens 115-123 15648573-6 2004 The initial rate of lysozyme release was varied depending on the length of the ethylene glycol chains possessed by a network polymer and the content of the phosphate-carrying monomer unit. Phosphates 156-165 lysozyme Homo sapiens 20-28 15648573-7 2004 Lysozyme released from the phosphate-carrying hydrogel was proved to retain enzymatic activity at a level similar to the activity of lysozyme, which had been kept in buffer solution. Phosphates 27-36 lysozyme Homo sapiens 0-8 3028504-2 1987 Protein is mainly associated in 0.01 phosphate buffer (pH 7.3) at 5-30 degrees C. Formation of the complex of lysozyme with competitive inhibitor (3-N-AGA) leads to changes of tau M. It may be due to a decrease of polymerization degree and increase of the protein packing. Phosphates 37-46 lysozyme Homo sapiens 110-118 9505202-0 1997 Lysozyme loading and release from hydrogels carrying pendant phosphate groups. Phosphates 61-70 lysozyme Homo sapiens 0-8 9505202-2 1997 The phosphate-carrying monomer yielded anionic hydrogels, which formed ionic complexes with the cationic protein, lysozyme. Phosphates 4-13 lysozyme Homo sapiens 114-122 9505202-3 1997 It was shown that the amount of complexed lysozyme reached 2.1 g g-1 dry gel, corresponding to 1.3 x 10(-3) mol phosphate group per gram lysozyme, when 40 mol% of phosphate-carrying monomer was incorporated in a hydrogel. Phosphates 112-121 lysozyme Homo sapiens 42-50 9505202-3 1997 It was shown that the amount of complexed lysozyme reached 2.1 g g-1 dry gel, corresponding to 1.3 x 10(-3) mol phosphate group per gram lysozyme, when 40 mol% of phosphate-carrying monomer was incorporated in a hydrogel. Phosphates 163-172 lysozyme Homo sapiens 42-50 35260871-2 2022 The zeta potential of lysozyme varies significantly at the same buffer concentration, in the order Tris > phosphate > citrate, with citrate even inverting the zeta potential, usually positive at pH 7.15, to a negative value. Phosphates 106-115 lysozyme Homo sapiens 22-30 30665033-8 2019 Electrochemical properties of selected BQs were monitored using cyclic voltammetry in phosphate buffered aqueous solution, and it was found that quinone reduction potentials correlate well with their reactivity trend toward lysozyme. Phosphates 86-95 lysozyme Homo sapiens 224-232 33676694-5 2021 Thanks to the recognition sites of phosphate and the template-shaped cavities, Fe3O4@TiO2@Lys MIPs showed great sensitivity (0.01 ng*muL-1) and selectivity (Lysozyme: BSA: beta-casein = 1:100:100, mass ratio) in standard phosphoprotein solution. Phosphates 35-44 lysozyme Homo sapiens 157-165 3697362-3 1986 The laser Raman spectra of human airway lysozyme and hen egg-white lysozyme in phosphate buffer solution (pH 7.2) are recorded in the range 300-1900 cm-1 at 488 nm. Phosphates 79-88 lysozyme Homo sapiens 40-48 3697362-3 1986 The laser Raman spectra of human airway lysozyme and hen egg-white lysozyme in phosphate buffer solution (pH 7.2) are recorded in the range 300-1900 cm-1 at 488 nm. Phosphates 79-88 lysozyme Homo sapiens 67-75 31330280-8 2019 Lysozyme can be adsorbed using 20 mmol/L phosphate buffer (pH 7.0) and eluted with 20 mmol/L phosphate buffer (pH 2.0). Phosphates 41-50 lysozyme Homo sapiens 0-8 30912776-2 2019 In this article, we have studied the interaction of citrate-capped GNPs of 16, 28, 41, and 69 nm sizes with Lyz by the non-destructive label-free second harmonic light scattering (SHLS) technique at physiological pH in phosphate buffer. Phosphates 219-228 lysozyme Homo sapiens 108-111 25728660-8 2015 The adsorbed lysozyme can be eluted using 20mM phosphate buffer (pH 7.0) containing 1.0M NaCl with a recovery of 96%. Phosphates 47-56 lysozyme Homo sapiens 13-21