Sentence examples for binding assays indicate that from inspiring English sources

RNA footprinting, chemical interference, and binding assays indicate that a minimum of a 5 bp stem capped with a NGNN tetraloop is required for Rnt1p binding[17], [17].

In vitro binding assays indicate that P1 directly binds the Zmf3' h1 promoter.

Our genome-wide data and in vitro binding assays indicate that Msi proteins act by binding UAG-containing motifs at 3' UTRs of messages.

Another less likely possibility, which is in contradiction with earlier in vitro binding assays indicating that replicase does not bind single-stranded sRNAs [25], [28], is that the replicase binds only one of the two strands of sRNA duplexes and exhibits some kind of 5' nucleotide preference similar to that of AGO proteins.

Results of TUNEL and Annexin-V binding assays indicated that the decreased viability of SPHK1-downregulated cells was due to increased apoptosis susceptibility (Figure 2D).

SARS-CoV antibody binding assays indicated that SARS specific antibodies inhibited SARS-CoV viral replication.

Competitive binding assays indicated that 17β-estradiol, bisphenol A, and diethylstilbestrol shared a common membrane-binding site.

Direct binding assays indicated that the O-GlcNAc modification slightly decreased the strength of the NTR·FG interaction.

RNA binding assays indicated that CstF-64 interacts with UUUU with a spacing of 15 30 nucleotides downstream of the 3'-processing site [ 4].

Previously, solid phase binding assays indicated that the Importinβ double mutant (I178D/Y255A, termed ImportinβDA) has a more than 60-fold lower Kd for binding to full-length Nup153FG as compared to Importinβ WT (Bednenko et al., 2003).

DOI: http://dx.doi.org/10.7554/eLife.06547.005 Fluorescence polarization (FP) binding assays indicated that ULK3 interacted more tightly with IST1 (K D ∼ 0.2 µM) than with other ESCRT-III proteins (K D ∼100 µM).