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All binding assays were done in duplicate.
Competition binding assays were done at 30 nM of [3H]-resveratrol in the presence of increasing concentration of cold resveratrol ranging from 0.1 nM to 100 µM.
All binding assays were done in triplicates.
Carbohydrate binding assays were done similarly as described previously [ 13].
Protein expression, purification, and retinol binding assays were done as for wild-type mSAA3.
To identify which Gα subunit is involved in the AprA signal transduction pathway, similar binding assays were done with membranes from cells lacking Gα2, Gα8, Gα9, or Gβ.
Similar(53)
Radioreceptor binding assay was done for β2-adrenoceptors using specific ligand, [3H] propranolol and gene expression studies of β2-adrenoceptors, transcription factor CREB, insulin receptors and Akt were also done using specific probes.
The flow cytometry-based competitive binding assay was done by B.Z.
All assays were done in duplicate.
Replicate assays were done.
The overlay protein-binding assay was done using rRH5 or native parasite supernatant (overnight) and erythrocyte ghosts.
More suggestions(12)
binding assays were generated
binding assays were performed
binding assays were prepared
binding assays were resolved
binding assays were included
binding assays were annealed
binding assays were repeated
binding assays were analyzed
binding assays were substituted
binding assays were used
binding assays were carried
binding assays were conducted
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