ライフサイエンスコーパス: potassium phosphate

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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 All cells contain much more potassium, phosphate, and transition metals than modern

7 In the presence of potassium phosphate at pH 7.4, MutL forms primarily stab

8 rom alpha-fluoroindanones in the presence of potassium phosphate base during the reactions.

9 socratic mobile system consisting of 17.5 mM potassium phosphate buffer (ph 6.5) and methanol (30:70)

10 d MnCl2.4H2O) concentrations and buffers/pH (potassium phosphate buffer pH 6-8, Tris buffer pH 8-10)

11 cell-free system is 1.84 mM-1 min-1 (100 mM potassium phosphate buffer, 5% ethanol, pH 7.5, 25 degre

12 tored at micromolar concentrations in 0.05 M potassium phosphate buffer, pH 7.0, at 10 degrees C.

13 d electrode is incubated in pH 3.0 of 0.10 M potassium phosphate buffer-based cocktail containing ani

14 V in steps of adding a glucose solution to a potassium phosphate buffer.

15 SSPE, PBS, TRIS, MES, sodium phosphate, and potassium phosphate buffers, and found that PBS and MES

16 The sucrose-potassium phosphate-glyoxylic acid method was also used

17 The open-state crystals, in 1.8 M potassium phosphate, have an expanded unit cell dimensio

18 stallizes from poly(ethylene glycol) 8000 in potassium phosphate in space group P2(1)2(1)2 with cell

19 sorbed at low ionic strength (pH 7.0, 4.4 mM potassium phosphate) onto 10 microm diameter gold partic

20 olumns with a mobile phase of methanol:10 mM potassium phosphate (pH 7.2):1 M tetrabutylammonium dihy

21 mutants of r Hb S were carried out in 1.8 M potassium phosphate (pH 7.34) by a temperature jump from

22 e the equilibrium solubility (Csat) in 0.1 M potassium phosphate (pH 7.35) at 25 degrees C of the thr

23 Sedimentation equilibrium analysis in 0.1 M potassium phosphate, pH 5.7, shows (i) the strong and we

24 tion, measurements were carried out in 10 mM potassium phosphate, pH 5.7.

25 trile/2-propanol (3+1, v+v) followed by 0.1M potassium phosphate, pH 6.7, and (2) purification using

26 obtained at 15 000 rpm for mixtures in 10 mM potassium phosphate, pH 7.5, by means of the psi functio

27 under a range of salts (potassium chloride, potassium phosphate, potassium acetate and sodium acetat

28 icular, we examined the effect of sodium and potassium phosphate salts and the detergent beta-octylgl

29 1.03 V vs Ag/AgCl in aqueous buffered (0.2 M potassium phosphate) solution as found by square wave vo

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