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Tests for binding properties were performed by the company DiscoverX (www.discoverx.com), using a concentration of 1 µM against ALK, MET and EGFR variants L858R and L858R_T790M) using KdELECT and scanKINETIC from DiscoverX [124, 125].
Similar(59)
My properties were performing fine.
Many of these studies also used whole ECMPs with multiple binding sites so they were unable to investigate the role of CAMs in maintaining pluripotency, and little characterisation of surface properties was performed.
Further evaluation of physicochemical properties was performed.
Subjective assessment of product properties was performed by subject questionnaire.
An investigation of rhesus relaxin-3 bioactivity and RXFP1 binding properties was also performed.
Molecular replacement and refinement were performed using CCP4 and the carbohydrate binding properties were described by affinity assays and computational docking.
The binding properties were analyzed in competitive binding, internalization, and cell surface retention experiments.
The hypothesized binding properties were tested experimentally.
Ligand binding properties were assessed in 2(125I -iodomelatonin (125I -iodomelatoninn and competition binding experiments (Table 3).
Binding studies concerning the number of binding sites and apparent binding constant Kb were performed by fluorescence quenching method.
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