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The selectivity of MIP towards the template was confirmed by comparing its binding with structural analogues of phosphonate esters.
The presence of zinc oxide nanocrystals in SiO2/Si track template was confirmed by X-ray diffraction analysis.
The predicted binding mode of the novel cyclic sulfone HEA core template was confirmed in a X-ray co-crystal structure.
The complete removal of the polymer template was confirmed by thermogravimetric analysis (TGA) of the composite microspheres (Fig. 3).
Integrity of each cDNA template was confirmed by the amplification of a ribosomal L8 protein encoding gene (CquiRpL8, XM_001841875).
Integrity of each cDNA template was confirmed by amplification of a "housekeeping" gene encoding ribosomal protein L8 (CquiRpL8, GenBank accession XP_001841927).
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The formation of hydrophobic anti-adhesion layer on the surface of the AAO templates was confirmed by contact angle measurement which was determined to be 150° as shown in Figure 1(b).
Integrity of cDNA templates was confirmed by amplification of "housekeeping" genes encoding actin and RpL8.
Presence of the expected 100-base pair SAGE templates was confirmed using an Agilent Bioanalyzer (High Sensitivity DNA Assay).
The formation and stability of pure rutile fully hollow nanotubes, after removal of carbon nanotubes used as templates is confirmed by 3D electron tomogram analysis.
The original templates were confirmed to be inactivated by streaking onto the chloramphenicol/ampicillin plates.
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