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1 ly formed product resulted only when samples were boiled, alternative methods of terminating cyclase
2 timation of protein contents in samples that were boiled, autoclaved or dry-heated at <=149 degrees C
3 ccase from cell wall preparations after they were boiled in 1% sodium dodecyl sulfate, as was the pre
4 IP of all Bdr paralogs when the cell lysates were boiled prior to addition of the precipitating antib
6 n reaction mixtures containing ATP and MgCl2 were boiled to terminate the enzyme assay, a cAMP-like d