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Endogenous mRNA was removed by treatment with 75 U/mL S7 MNase and 1 mM CaCl 2 at 23 C for 5 min, followed by nuclease inactivation with 2.4 mM EGTA
Development and properties of beta-glucuronide linkers for monoclonal antibody-drug conjugates
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Front Physiol 12:710429
Thus it is presumed that the expression of GshF driven by GAP promoter of S
(1987 b )
