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Our in vitro binding assay allowed assessment of whether parts of the trigger flanking the miRNA-binding site might also influence ZSWIM8 recognition
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Background subtraction was done using the scattering from the storage buffer (150mM NaCl, 20mM Tris-HCl, pH 7.5) and by scaling the buffer and sample intensities at the q ∼ 2 Å -1 water peak
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