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The results showed that the AG-SEP3 complex activated the LUC reporter as expected, while 35Spro-mTCP4, in which miRNA319-resistant mTCP4 was driven by a CaMV 35S promoter, repressed LUC expression (Fig

Similarly, a lipase derived from Halocynthiibacter arcticus displayed a temperature optimum of 20 C

Reactive matrix-assisted laser desorption/ionization mass spectrometry imaging using an intrinsically photoreactive paterno-buchi matrix for double-bond localization in isomeric phospholipids
