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Results 1 - 10 of 10
EC Number Activating Compound Commentary Reference
Display the word mapDisplay the reaction diagram Show all sequences 4.6.1.18butanediyl-1,4-bis(hydroxyethyl methyl hexadecyl ammonium bromide) - 729838
Display the word mapDisplay the reaction diagram Show all sequences 4.6.1.18hexanediyl-1,6-bis(hydroxyethyl methyl hexadecyl ammonium bromide) - 729838
Display the word mapDisplay the reaction diagram Show all sequences 4.6.1.18KCl - 134536
Display the word mapDisplay the reaction diagram Show all sequences 4.6.1.18NaCl - 134536, 134538, 134556
Display the word mapDisplay the reaction diagram Show all sequences 4.6.1.18pentanediyl-1,5-bis(hydroxyethyl methyl hexadecyl ammonium bromide) - 729838
Display the word mapDisplay the reaction diagram Show all sequences 4.6.1.18Sodium citrate - 134536
Display the word mapDisplay the reaction diagram Show all sequences 4.6.1.18NaCl at 0.1-0.25 M 134538
Display the word mapDisplay the reaction diagram Show all sequences 4.6.1.18Chloroquine at 0.13 mM 134522
Display the word mapDisplay the reaction diagram Show all sequences 4.6.1.18sulfate decreases the distance between the catalytic His residues and increases the globular compactness 682695
Display the word mapDisplay the reaction diagram Show all sequences 4.6.1.18alkanediyl-alpha,omega-bis(hydroxyethyl methyl hexadecyl ammonium bromide) the cationic gemini surfactants slightly activate and stabilize RNase A below their critical micelle concentrations at pH 5.0. The cationic gemini surfactant with the shorter spacer interacts more efficiently with RNase A than those with longer spacers, two-transition model, UV, circular dichorism and fluorescence spectroscopies, overview 729838
Results 1 - 10 of 10