ライフサイエンスコーパス: binding method

1 domains was assayed with a radioactive Ca2+-binding method.

2 P nick end labeling (TUNEL) or the annexin V binding method.

3 a related, sequential injection competitive binding method.

4 nclusions were confirmed by a novel antibody binding method.

5 tested in a CD30+ cell line by the annexin V-binding method.

6 cessfully in 12 algal species using this dye binding method.

7 l, kinetic, chromatographic, and radioligand binding methods.

8 ic enzyme using stopped-flow and equilibrium binding methods.

9 , surface plasmon resonance, and competitive binding methods.

10 es using identical quality-controlled ligand-binding methods.

11 g equilibrium and nonequilibrium radioligand binding methods.

12 ing steady-state kinetic and pre-equilibrium binding methods.

13 cone and plate(let) analyzer and fibrinogen binding methods.

14 serotonin receptor subtypes by use of ligand-binding methods and functional assays.

15 eC approach can compliment existing in vitro binding methods, and can also provide unique in vivo ins

16 Using both an improved direct binding method as well as a novel inhibition assay, we s

17 nalysis using recently developed fluorescent binding methods corroborates the finding that the Motuls

18 Results indicate that a peptide binding method coupled with mass spectrometric detection

19 Several high-throughput protein-DNA binding methods currently available produce highly repro

20 roach is the competition-association kinetic binding method first described in the 1980s.

21 a genetic algorithm and nonorthogonal-tight-binding method, followed by a refining and biased search

22 ate the value of the fluorescent lipid probe binding method for assisting structure-based studies of

23 at combines (i) the density-functional tight-binding method for dynamic generation of property traini

24 The Coomassie brilliant blue dye-binding method for protein assay has become important re

25 alidated scintillation proximity assay (SPA) binding method for quantitation of (3)H-labeled d-lyserg

26 e creation of a highly sensitive radioactive binding method for quantitatively measuring FR expressio

27 nctional theory and density functional tight binding methods for finite-size SWNT models with n = 3,

28 introduce chemical conjugation and physical binding methods for monovalent and polyvalent surface en

29 independent heparin-binding domain, solution binding methods have been used in combination with NMR a

30 YPK were measured, where possible, by direct binding methods in the absence of ADP.

31 ed compared with the state of the art ligand-binding methods including COACH and TargetS for high-acc

32 The DNA-assisted binding method may also prove useful in the study of oth

33 by eliminating two steps required in the dye-binding method: removal of interfering lipophilic compou

34 density-functional and coarse-grained tight-binding method reveals that hBN's bi-periodic sinusoidal

35 n of these hydrogels as low as other antigen-binding methods such as ELISA or fluorescence-tag system

36 ymmetry, interatomic force fields, and tight binding methods to build many possible 3D conformers fro

37 those obtained using the traditional filter-binding methods to measure RNA polymerase activity.

38 A dye-binding method using Acid Orange 12 was investigated reg

39 We validated the DNA-assisted binding method using heterodimerizing coiled-coil protei

40 The Slater-Koster tight-binding method was adopted for geometry optimization and