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We succeeded in a simple procedure where CPO is titrated with purified equine butyrylcholinesterase.
Picric acid is a much stronger acid than phenol; it decomposes carbonates and may be titrated with bases.
TPR2A (20 μM) loaded with equimolar Tb3+ was titrated with increasing concentrations of EGFP-C90 (0–15 μM).
To obtain KD values, 20 μM of the LBT-TPR2A-Tb3+ complex was titrated with increasing concentrations of EGFP-C90.
The extracellular solution included 160 mM MeSO3K, 10 mM HEPES, pH 7.0, 2 mM MgCl2 titrated with MeSO3H.
Some solutions were titrated with 0.1 mol/dm^3 HCl, or acetic acid, to be pH = 4.5.
Two oxide ion acceptors (acids), NaPO3 and Na4P2O7 were titrated with oxide ion donors (bases) in fused KNO3.
The enzyme immobilized nanoparticles were titrated with different concentrations of H2O2 and a fixed concentration of O-phenylenediamine (OPD).
50 μM of reduced, 15N-labelled Cc in 5 mM sodium phosphate buffer (pH 6.3) was titrated with unlabeled 14-3-3ε 14-3-3ε 14-3-3εfer.
The solution was finally titrated with 0.0045 N-KOH.
Finally the released EDTA is back titrated with lead nitrate.
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