Sentence examples for affinity 1 from inspiring English sources

A change in stereochemistry results in a binding decrease 2. This position is quite tolerant to some (but not all) substitutions for other l-aminoacids with bicylic aromatic side chains 3. Monocyclic aromatics like phenylalanine derivatives cause a decrease in affinity 1.

Although the fluorescence signal change was small, this sensor had high cGMP affinity (1 µM) and selectivity for cGMP over cAMP (400-fold) comparable to cGES-DE5 (Figure 1C).

NOD SSS events were detected in the Fc receptor, IgG high affinity 1 (Fcgene gene.

Ubiquitylation assays were performed as described previously (Elderkin et al., 2007 ), using 300 ng E1 (Boston Biochem), 300 ng UbcH5c (affinity), 1 μg ubiquitin (Sigma), 0.0037 MBq I125-Ub (Perkin Elmer), the indicated concentration of E3, and 1.5 μg oligonucleosome.

We have previously reported SH-SAMMS to have much higher affinity (1 × 10 fold higher in Kd) and capacity (20-fold higher in capacity) for Hg II) than GT-73, all measured in filtered groundwater.

Of the several CXCR4 antagonists available, 4F-benzoyl-TN14003 (BKT140; Figure 1A) was chosen for the present study based on two reasons: (i) BKT140 has a high binding affinity (1 nM) toward CXCR4, and (ii) BKT140 is safe in vivo.

For FGFR2, alternative splicing of the second half of the third Ig-like domain, involving exons IIIb and IIIc, is a mutually exclusive choice that affects ligand binding specificity and affinity [ 1, 2, 3].

Sigma receptors are membrane-bound proteins that bind several psychotropic drugs with high affinity [1].

DPI-VTK demonstrated significantly greater binding affinity (1/KD) to apatite surfaces compared to VTK, phosphorylated VTK (VTKphos), DPI-VTKphos, RGD-VTK, and peptide-free apatite surfaces (p < 0.01), while significantly increasing hBMSC adhesion strength (τ50, p < 0.01).

TMP-tag (18 kDa) was derived from E. coli dihydrofolate reductase (eDHFR), which binds the small-molecule inhibitor TMP with high affinity (∼1 nM K D) and selectivity (affinities for mammalian DHFRs are K D > 1 μM).

From Freundlich isotherm, it can be deduced that the values for the biosorption affinity, ({1 mathord{left/ {vphantom {1 n}} right. kern-0pt} n}), for the uptake of CR, MB, Cd2+ and Pb2+ onto TISW were 0.93, 2.41, 0.43 and 0.53, respectively.