Sentence examples for binding we prepared a from inspiring English sources

Because the steric structure of the peptide and some of the amino acid residues were related to the binding, we prepared a peptide-2, to which the N- and C-terminals of peptide-1 were alternated.

To examine the role of conserved SMN residues in Gemin2 binding, we prepared a series of SMN26 51 alanine substitutions and tested them for binding to Gemin295 280.

To assess the energetic contribution of the ESS3b motif to high-affinity UP1 binding, we prepared a series of SL3ESS3 constructs in which each position of the 5′-GAUUAG-3′ apical loop was mutated to a cytosine residue.

To investigate whether the STDE is involved in the binding, we prepared a longer construct (residues 351 439) containing both acidic regions and performed the NMR titration experiment under the same conditions (Supplementary Figure 4).

Thus, in an attempt to reveal how chelate structure influenced (AlF 2+ binding, we prepared three new pretargeting peptides, each with a different ligand.

To investigate how cyclic permutation of the two nitrogen atoms of a pyrazole might affect ER binding affinity, we prepared a new pyrazole core isomer, namely a 1,3,4-triaryl-5-alkyl-pyrazole 1,3,4-triaryl-5-alkyl-pyrazole 1,3,4-triaryl-5-alkyl-pyrazole 1,3,4-triaryl-5-alkyl-pyrazole 1,3,4-triaryl-5-alkyl-pyrazole

For RpoD or RpoS binding site identification, we prepared a ChIP library from cells harvested in exponential phase and stationary phase, respectively.

Since it was previously demonstrated that catecholamine shows strong and robust binding to TiO2, we prepared a TiO2-coated quartz substrate and formed PMAP layer on the TiO2 surface.

To investigate their CL4-binding, we prepared the recombinant proteins of the binders and investigated their interaction with CL4 by ELISA with CL-BVs.

To understand the biological role of arginine methylation of RNA-binding protein, we prepared and characterized a mouse monoclonal antibody against asymmetric dimethylarginine of TLS.

Based on these 12 predicted binding sites, we prepared 11 probes for EMSAs (see Fig. S10 and Table S4).