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The specificity of binding was compared with the binding of the antibodies to recombinant pro-OP-1 pro-OP-1 pro-OP-1
This list of genes associated with significant changes in STAT3 binding was compared with the list of genes with significant expression changes using the online tool Galaxy (Giardine et al. 2005; Blankenberg et al. 2010; Goecks et al. 2010).
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Known motifs in AgtGS predicted to play a role in catalysis and/or binding were compared with SSs analysed.
The SAR found for hemoglobin binding were compared with the SAR found in the literature for mutagenicity, carcinogenicity, and cytotoxicity of arylamines and nitroarenes.
The motif identified by MEME analysis of putative MrpC binding sites was compared with binding motifs stored in RegTransBase [ 78] using TOMTOM [ 76].
This binding energy was compared with the binding energy of influenza NP418 epitope to HLA B*3501 and found to be the same as the predicted epitope (−7.6 kcal/mol, Figure 2, A and B).
Finally, the mtDNA variation pattern in predicted TFBS, occurring within ChIP-seq negative-binding sites, was compared with ChIP-seq positive-TFBS (CPR).
Ex vivo tumor binding of DAB4 was compared with that of TNT1 mAb.
A similar decline in half-life was observed when afucosylated trastuzumab, exhibiting increased binding to hCD16A, was compared with trastuzumab in hCD16A transgenic mice [ 36].
Peptide binding to each receptor was compared with IgG1 binding (equivalent to 100%) (Fig. 5 A ).
The binding of b-nisin was compared with a known lipid II binding probe, fluorescein-vancomycin, (f-vancomycin).
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