Sentence examples for most robust binding from inspiring English sources

We therefore examined the ability of KSHV1 51 EGFP) and RFHV1 50 EGFP) to bind to importin α, using importin α3, which showed the most robust binding in Figure 5.

Strong binding of KSHV1 51 EGFP) and RFHV1 50 EGFP) was detected to importins α1, α3, α5, α7 (Fig. 5, lanes 3,4,5 and 6) with α3 showing the most robust binding.

Our data demonstrate widespread and reproducible RBM47 binding to target mRNAs predominantly in introns and 3′UTRs, with the most robust binding occurring in 3′UTRs.

As has been previously described for the n-ELAV proteins (Ince-Dunn et al., 2012), identification of the most robust binding through increased stringency of cluster definition led to an increase in proportional binding in 3′UTR regions.

(D ) Increasing the stringency of biologically reproducible RBM47 binding site definition reveals predominant binding in 3′UTRs and intronic regions of target transcripts, with the most robust binding (tags per binding site) evident in 3′UTRs.

The next most robust binding motifs corresponded to 2 transcription factors, NK2 transcription factor-related locus 5 (NKX2-5) and coiled-coil domain containing 6 (CCDC6), which had an enriched motif in over 90% of the resampled gene sets (99/100 and 91/100 enrichment frequency, respectively).

Although a number of biophysical methods are available, protein-based NMR spectroscopy is the most robust and reliable method to study ligand binding.

The binding of pimonidazole adducts is perhaps the most robust and widely accepted marker of cellular hypoxia (Varia et al, 1998; Nordsmark et al, 2001; Raleigh et al, 2001; Kaanders et al, 2002).

Aptamers are single-stranded DNA or RNA oligonucleotides that bind to target molecules with robust binding affinities.

However, when data from competitive ligand binding assays are compared with medaka gene expression data, it is evident that the compounds that elicited the most robust biomarker induction in medaka, i.e., E2β and E3, both exhibited preferential binding affinity for the two mERβ subtypes over mERα.

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