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1 P can strongly bind only its own PB in 0.8 m potassium phosphate.
2 igands that were aggregated at pH 7 in 70 mM potassium phosphate, 100 mM KCl, 1 mM EDTA buffer also d
3 ed the non-idealities of solutions including potassium phosphate and other solutes.
4  an ATPS of 16% (w/w) 2-propanaol, 19% (w/w) potassium phosphate, and 5% (w/v) NaCl at pH 7.5.
5  and ethanol), type of salt (sodium citrate, potassium phosphate, and ammonium sulphate), pH, and NaC
6 -response relationships of sodium, chloride, potassium, phosphate, and calcium excretion were assesse
7                  All cells contain much more potassium, phosphate, and transition metals than modern
8                           In the presence of potassium phosphate at pH 7.4, MutL forms primarily stab
9 rom alpha-fluoroindanones in the presence of potassium phosphate base during the reactions.
10 socratic mobile system consisting of 17.5 mM potassium phosphate buffer (ph 6.5) and methanol (30:70)
11  to detect glucose or lactate in both 100 mM potassium phosphate buffer and artificial sweat.
12 ted best characteristics at pH 7.5 in 100 mM potassium phosphate buffer at an applied potential of +0
13 d MnCl2.4H2O) concentrations and buffers/pH (potassium phosphate buffer pH 6-8, Tris buffer pH 8-10)
14  cell-free system is 1.84 mM-1 min-1 (100 mM potassium phosphate buffer, 5% ethanol, pH 7.5, 25 degre
15 tored at micromolar concentrations in 0.05 M potassium phosphate buffer, pH 7.0, at 10 degrees C.
16 d electrode is incubated in pH 3.0 of 0.10 M potassium phosphate buffer-based cocktail containing ani
17     Lp(a) is then dialyzed for up to 24 h in potassium phosphate buffer.
18 V in steps of adding a glucose solution to a potassium phosphate buffer.
19  SSPE, PBS, TRIS, MES, sodium phosphate, and potassium phosphate buffers, and found that PBS and MES
20  analytes were chosen for aggregating AgNPs, potassium phosphate for neutralizing the charges and a d
21                                  The sucrose-potassium phosphate-glyoxylic acid method was also used
22            The open-state crystals, in 1.8 M potassium phosphate, have an expanded unit cell dimensio
23 stallizes from poly(ethylene glycol) 8000 in potassium phosphate in space group P2(1)2(1)2 with cell
24 h hydroxyl groups (sodium phosphate dibasic, potassium phosphate monobasic, and glucose) exhibited in
25 sorbed at low ionic strength (pH 7.0, 4.4 mM potassium phosphate) onto 10 microm diameter gold partic
26 olumns with a mobile phase of methanol:10 mM potassium phosphate (pH 7.2):1 M tetrabutylammonium dihy
27  mutants of r Hb S were carried out in 1.8 M potassium phosphate (pH 7.34) by a temperature jump from
28 e the equilibrium solubility (Csat) in 0.1 M potassium phosphate (pH 7.35) at 25 degrees C of the thr
29  Sedimentation equilibrium analysis in 0.1 M potassium phosphate, pH 5.7, shows (i) the strong and we
30 tion, measurements were carried out in 10 mM potassium phosphate, pH 5.7.
31 trile/2-propanol (3+1, v+v) followed by 0.1M potassium phosphate, pH 6.7, and (2) purification using
32 obtained at 15 000 rpm for mixtures in 10 mM potassium phosphate, pH 7.5, by means of the psi functio
33  under a range of salts (potassium chloride, potassium phosphate, potassium acetate and sodium acetat
34 ion (polyetilenglycol (PEG, 1.6-2.4 g/L) and potassium phosphate (PP, 1-1.3 g/L) was applied for XR p
35 icular, we examined the effect of sodium and potassium phosphate salts and the detergent beta-octylgl
36     To achieve this, PFASs were reacted with potassium phosphate salts under solvent-free mechanochem
37 1.03 V vs Ag/AgCl in aqueous buffered (0.2 M potassium phosphate) solution as found by square wave vo
38 lated by Ac~P and either sodium phosphate or potassium phosphate, which are not phosphate donors, ful