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Ligand binding assay is associated with a multiplicity of specificity issues (Findlay, 2008).
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PCT assay was associated with a CRP one in 94.9%.
The in vitro pVHL-HIF-2α binding assay was performed according to a previously published protocol67.
A competitive flow cytometry-based binding assay was performed to further validate the identified hCXCL1 binding epitopes in different ELR+ CXC chemokines.
A competitive binding assay was also performed using unlabelled DNA target to demonstrate its applicability to real sample analysis.
In order to determine the binding affinity, a competitive cell binding assay was performed.
To determine if adenine nucleotides directly contribute to the regulation of GRP94 peptide binding activity, an in vitro peptide binding assay was developed.
The binding assay was similar to the selection procedure.
The binding assay was described previously.
It was reported that GABP binding affinity is associated with bidirectional transcriptional activity in a luciferase transfection assay [ 11].
We found that binding to ICAM-1Reference is associated with CM, and levels of binding of isolates from patients with this clinical syndrome were found to be significantly higher than UM cases when using flow-based assays.
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