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3 nce detection and electrochemical control of biospecific binding has been developed and investigated
4 the high binding avidity and selectivity of biospecific binding molecules together with highly sensi
6 tudies ranging from molecular electronics to biospecific cell-based assays and biomolecular microarra
8 ge and quantify biochemiluminescence coupled biospecific enzymatic reactions to detect analytes in bi
9 affinities using a surface plasmon resonance biospecific interaction (BIAcore) assay showed the wild-
10 amide, and lactosyl ceramide using real time biospecific interaction analysis (surface plasmon resona
13 by coupling a polymerization initiator to a biospecific interaction and inducing inline atom transfe
14 ify the GST enzyme concentration through its biospecific interaction with tripeptide reduced glutathi
15 ption, which could likely be used to promote biospecific interactions and/or to suppress nonspecific
16 c flexibility and utility of this method for biospecific interactions by installing aminooxy terminat
17 l to create a platform capable of monitoring biospecific interactions directly in liquid at very low
20 roscopy using BIAcore technology to evaluate biospecific interactions, demonstrating the increasing p
23 layer, mass and viscosity variations of the biospecific layer can be detected by monitoring changes
25 and together competitively incubated on the biospecific MDEA ECC 5037-Pt|MGC|HCF|Hydrogel-NFO4 biotr
28 equipped with affinity purification tags and biospecific recognition domains usable as fluorescent la
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