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An amino acid sequence alignment comparison of the POM scFvs (the best binders) is shown in Supplementary Figure S6.
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The volume fractions of detected binders are shown in Table 5.
The chemical structures of the representative binders are shown in Fig. 1.
A deep insight into the cycling performance of the electrodes using three kinds of binder is shown in Fig. 5.
The roundness values of binders in different sections, made by using different quantities of binder, are shown in Fig. 3; the corresponding histogram is shown in Fig. 4.
The relationship between SP dosage with respect to the percentage of total dry weight of binder content is shown in Fig. 5.
Distribution diagrams of the binders in briquettes are shown in Fig. 2 (agglomerated binders are shown as circles with equivalent areas while dispersed binders are neglected).
A comparison of CuO electrodes before and after cycle used SBR+CMC (a, b, c, d) and LA133 (e, f, g, h) as binder was analyzed by SEM and is shown in Fig. 7.
It is shown, in our work, the capacities of the conventional PTFE and PVDF binders drop very fast.
Comparison of percentage specific binders from pannings of primary libraries (expressing random peptides) vs. secondary libraries (based on target-specific primary surrogates) is shown in this Table.
Binding of MBP-NPMmutANES (a moderate CRM1 binder) and MBP-SNUPNNES (a weak binder) is shown on the rightmost panel for reference.
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