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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 ic enzyme using stopped-flow and equilibrium binding methods.
8 , surface plasmon resonance, and competitive binding methods.
9 es using identical quality-controlled ligand-binding methods.
10 g equilibrium and nonequilibrium radioligand binding methods.
11 ing steady-state kinetic and pre-equilibrium binding methods.
12 cone and plate(let) analyzer and fibrinogen binding methods.
13 l, kinetic, chromatographic, and radioligand binding methods.
15 eC approach can compliment existing in vitro binding methods, and can also provide unique in vivo ins
18 a genetic algorithm and nonorthogonal-tight-binding method, followed by a refining and biased search
19 ate the value of the fluorescent lipid probe binding method for assisting structure-based studies of
21 alidated scintillation proximity assay (SPA) binding method for quantitation of (3)H-labeled d-lyserg
22 e creation of a highly sensitive radioactive binding method for quantitatively measuring FR expressio
23 nctional theory and density functional tight binding methods for finite-size SWNT models with n = 3,
24 independent heparin-binding domain, solution binding methods have been used in combination with NMR a
26 ed compared with the state of the art ligand-binding methods including COACH and TargetS for high-acc
28 by eliminating two steps required in the dye-binding method: removal of interfering lipophilic compou
29 n of these hydrogels as low as other antigen-binding methods such as ELISA or fluorescence-tag system
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