ライフサイエンスコーパス: MOPS

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1 d large decreases in k(cat) values in pH 7.5 MOPS buffer, but only exhibited small changes in k(cat)/

2 ity relative to wild-type activity in pH 7.5 MOPS buffer, suggesting that the original glutamate resi

3 relative to those of the wild type in pH 7.5 MOPS buffer, while other substitutions (E62A, -C, -H, -Q

4 addition of morpholinepropanesulfonic acid (MOPS) or Tris-HCl (pH 7.5) results in a dramatic increas

5 MES) and 3-N-morpholinopropanesulfonic acid (MOPS) did not bind copper and would be good choices for

6 0165 M 3-(N-morpholino)propanesulfonic acid (MOPS) and a 24-h incubation time, all of the isolates we

7 ses in 3-(N-morpholino)propanesulfonic acid (MOPS) buffer and characterize the hydrodynamic aspects o

8 inimal 3-(N-morpholino)propanesulfonic acid (MOPS) medium containing different amounts of IPTG.

9 buffer 3-(N-morpholino)propanesulfonic acid (MOPS), which has a very small temperature coefficient.

10 r with 3-(N-morpolino)propane sulfonic acid (MOPS) led to increased interparticle interference, consi

11 fer [3-(N-morpholino)-propanesulfonic acid] (MOPS).

12 negligible complex properties (e.g., MES and MOPS).

13 ng iron(III) complexes between 1-octanol and MOPS buffer (pH 7.4) are also influenced.

14 er and 9.2 x10(-4) cm(3)mol/g(2) for BPTI in MOPS.

15 Unexpectedly, however, when grown in MOPS minimal medium, in mixed cultures, more hmp mutant

16 = +15.1 +/- 0.5 degrees C, for 100 nM MB in MOPS buffer.

17 microM in Tris buffer or from 6.7 microM in MOPS buffer to 50 microM in phosphate buffer when tested

18 igh external osmolalities (1.02-2.17 Osm) in MOPS-buffered minimal medium (MBM) containing 1 mM betai

19 s (e.g., CHES/LiOH, TAPS/LiOH, Tricine/LiOH, MOPS/LiOH, MES/LiOH, and acetic acid/LiOH).

20 he broth macrodilution method with the lower MOPS concentration correlated with the results of the 24

21 The lower MOPS concentration may also be a useful modification to

22 sociation constant was 0.25 microM in 0.01 M MOPS Na(+) at pH 7.2.

23 esting in microdilution panels, the 0.0165 M MOPS concentration combined with 24 h of incubation appe

24 dilution method with both 0.165 and 0.0165 M MOPS.

25 art I of this paper series; e.g., CHES, MES, MOPS, Tricine were used to demonstrate behavior of such

26 ly investigated in 10 mM carbonate and 10 mM MOPS buffer, and in filtered natural freshwater.

27 ry stable (Kd = 6 pM) at 10 degrees C, 10 mM MOPS, pH 6.7.

28 a proximal 472-bp murine rod opsin promoter (MOPS) to drive ribozyme synthesis.

29 broth macrodilution method with the standard MOPS concentration did not correlate with any of the res

30 Using MOPS, we also observe temperature-dependent ET rate cons

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