ライフサイエンスコーパス: reciprocal plot

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1 doHcy) were obtained and evaluated as double-reciprocal plots.

2 MAO A, including biphasic kinetics in double reciprocal plots.

3 phosphatase both yielded intersecting double-reciprocal plots.

4 entration-dependent increase in slope of the reciprocal plots and in the apparent Km values with sphi

5 Double reciprocal plots and preincubation studies revealed S-ad

6 Reciprocal plots at varying fixed concentrations of the

7 nhibitor for GGPP, gave a competitive double reciprocal plot for varied concentrations of GGPP and in

8 Double reciprocal plots for coenzyme binding to DGD exhibit two

9 Curvature is observed in the double-reciprocal plots for product inhibition by NADH and the

10 Double reciprocal plots for the peptide mimic Cys-AMBA-Leu gave

11 Double-reciprocal plots for two-substrate kinetic data yielded

12 ady-state rate studies yield parallel double-reciprocal plots; however, we show that fluoride interac

13 The linearity of primary double-reciprocal plots, in the presence and absence of dead-en

14 o AMD Study), which were plotted on a double reciprocal plot of 1 / lesion size (disc area) vs 1 / ti

15 From a double-reciprocal plot of k(obs) versus [H(2)O(2)] at pH 10, we

16 Reciprocal plots of data collected with either ATP or L-

17 oth talnetant and osanetant displayed linear reciprocal plots of identical slope when [MePhe7]neuroki

18 Double reciprocal plots of initial rates versus concentrations

19 Double-reciprocal plots of initial velocities versus the varyin

20 control eyes fit a straight line on a double reciprocal plot (r2 = 0.98) after the introduction of ho

21 Double-reciprocal plots showed a competitive inhibition pattern

22 In this mechanism, double reciprocal plots will appear nearly parallel (as observe

23 Double reciprocal plots with N-methyl-L-tryptophan as the varie

24 Although the double-reciprocal plots with UTP produced parallel lines, initi

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