ライフサイエンスコーパス: maximum binding

1 Maximum binding affinity for artemisinin was shown by Aa

2 vely binds the alpha-anomer of GlcN6P with a maximum binding affinity of 0.36 mM and that binding is

3 ile maintaining a reasonably high, but below maximum, binding affinity.

4 , gelsolin is able to bind F-actin with half-maximum binding at 0.14 microM free Ca2+ concentration.

5 bind to C4S at as early as 14 h and exhibit maximum binding at 22 to 26 h postinvasion.

6 The maximum binding (B(max)) of trypsin to fAbeta 1-40 and f

7 gulation significantly increased (125)I-PDGF maximum binding (B(max)) to PDGF receptors on VSMCs with

8 ites on retina membranes (K(d) = 2.5-6.5 nM; maximum binding [B(max)] = 1-48 x 10(10) sites/retina).

9 six HMAbs have similar binding affinity and maximum binding, B(max), a relative indicator of epitope

10 , and a third GST-RyR construct demonstrated maximum binding between 150 and 450 mm NaCl.

11 , whereas hTRas010 inhibited over 90% of the maximum binding between the CR4-CR5 fragment of hTR (nuc

12 hTRas009 inhibited approximately 50% of the maximum binding between the pseudoknot fragment of hTR (

13 apparent dissociation constant of 130 pM and maximum binding (Bmax) of 240.0 fmol/mg protein.

14 chloride concentration caused a decrease in maximum binding but did not alter K(d) values, suggestin

15 125I-1E8 bound to MCF-7 cells; the maximum binding capacity (1.5 x 10(6) sites per cell) wa

16 nity for the GRP-R (Kd, 1.02 nmol/L), with a maximum binding capacity (Bmax) of 414 fmol/10(6) cells

17 The maximum binding capacity (Bmax) of the high-affinity rad

18 to membranes with high affinity (Kd = 6 nM); maximum binding capacity (Bmax) was 275 fmol/mg protein.

19 Equilibrium constant (KD), maximum binding capacity (Rmax) and Gb values for intera

20 -FES had a dissociation constant of 3 nM and maximum binding capacity 83 fmol/10(6) SKOV3 cells.

21 ibrium dissociation constant, Kd = 7 nM) and maximum binding capacity approximating 300,000 receptors

22 FHNP had a dissociation constant of 2 nM and maximum binding capacity of 18 fmol/10(6) cells, and (18

23 Equilibrium constant (KD) and maximum binding capacity of analyte (Bmax) values for th

24 Equilibrium dissociation constant (KD) and maximum binding capacity of analyte (Bmax) values for th

25 ascorbic acid increased the affinity and the maximum binding capacity of LPMO for cellulose.

26 The maximum binding capacity of the protein G-coupled membra

27 ndrance between GPVI molecules restricts the maximum binding capacity.

28 he lipids is consistent with a change in the maximum binding capacity.

29 tion of bound cofilin clusters, suggest that maximum binding cooperativity is achieved when 2 cofilin

30 For example, the maximum binding energy, -166.5 kJ mol(-1), occurs for th

31 The maximum binding force under a specific angle (optimal an

32 ates that are size- and shape-complementary: maximum binding is observed for dicarboxylic acids and d

33 omparable (90 and 130 pM, respectively), the maximum binding obtained with 125I-ET-3 was approximatel

34 Maximum binding occurs at low [glucose] (<5 mM) and mini

35 ), and Ile(190) as important determinants of maximum binding of (125)I-labeled bovine PTH-(1-34) and

36 f 8.9 +/- 1.9 microg of protein per ml and a maximum binding of 100 +/- 8 resonance units.

37 lso increases the affinity and decreases the maximum binding of ACP to FabG.

38 ession of cyclins A and B correlate with the maximum binding of B-Myb to these promoters.

39 (125)I were used to determine the timing of maximum binding of each anti-PSMA antibody fragment on t

40 Maximum binding of L-733,560 and most related analogs to

41 s with NhaA, (iv) whereas acidic pH inhibits maximum binding of Na(+) to NhaA, partial Na(+) binding

42 However, maximum binding of neurocan requires both the fibrinogen

43 tions (5-10 microM), defensin stimulates the maximum binding of plasminogen to HUVEC and to fibrin ap

44 ic-acid ratio identical to that required for maximum binding of the capsid protein to nucleic acid.

45 acid composition of the peptide, confers the maximum binding of the targeting domain to the staphyloc

46 ng of SL-ATP to this mutant P-gp resulted in maximum binding of two nucleotides; the binding affinity

47 The binding affinity (k) and the maximum binding (r(max)) for celecoxib to both natural a

48 sites (Kd = 31 nmol/L and 244 nmol/L) and a maximum binding ratio of 3.8 mol t-PA/mol fibrin.

49 The dissociation constant (Kd) and the maximum binding sites (Bmax) in a bovine membrane prepar

50 red auxilin, but less auxilin was needed for maximum binding than for maximum ATPase activity showing

51 Steric interference effects limit maximum binding to approximately 50% average occupancy i

52 of P. gingivalis LPS required to obtain half-maximum binding to CD14 was approximately 10-fold greate

53 ding, alters binding affinity, and increases maximum binding to polymerized fibrin, effects that may

54 ced the cGMP concentration required for half-maximum binding to the allosteric cGMP-binding sites fro

55 At even lower binding levels (1.4% of maximum binding), virus survival was 44%.

56 Maximum binding was achieved and K(m) and V(max) values

57 r a range from 0.05 to 10 mmol/L, and a half-maximum binding was attained at approximately 0.6 mmol/L

58 eract with the syntaxin-1 t-SNARE motif with maximum binding within the range of 20-50 muM Ca(2+).