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The guanine N1 base imino resonance at the site of conjugation was observed in isotope-edited N NMR experiments, suggesting that the conjugated guanine was inserted into the duplex and that the guanine imino proton was protected from exchange with water.
In addition, the shape of QDs after conjugation was observed through TEM.
Direct evidences of conjugation was observed from peaks at 1,910 1,970 cm−1 for C H alkyl stretching, 2,549 cm−1 due to S H deformation and 701 cm−1 for thiol stretching.
In contrast to deoxynivalenol plant metabolism, no glutathione conjugation was observed.
Transfer of resistance through conjugation was observed in 42/57 isolates.
Rapid conjugation was observed between the maleimide compound and the light chain of LC-V205C, whereas the sulfone conjugate was not extensively formed until 4 or 8 h.
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Considerable blue-shifts in the dyes' excitation wavelengths upon conjugation are observed.
Considerable variation in xenobiotic conjugation is observed as a result of altered expression of UDP-glucuronosyltransferases (UGTs) and sulfotransferases (STs).
Mass measurements indicated that both peptides had multiple heptose modifications; a mixed population of modified peptides, containing different numbers of heptose conjugations, was observed.
This is reflected in our experiments where conjugations are observed in ∼65% of the wells containing both NK cells and target cells approximately one hour after mixing.
Most successful conjugation strategy was observed in the case of PEI conjugates among which most efficient vector was PEI GO conjugate bearing glycine linker.
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