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. 2004 Jul;186(13):4254–4261. doi: 10.1128/JB.186.13.4254-4261.2004

TABLE 1.

Buffer formulations used in this studya

Test substance (concn in buffer) Mode of action Base buffer Solvent (%) Matched control buffer
Valinomycin (10 μM) K+ ionophore Valinomycin buffer MeOH (0.1) Valinomycin buffer + 0.1% MeOH
FCCP (10 μM) Protonophore PBS/G MeOH (0.1) PBS/G + 0.1% MeOH
Arsenate (50 μM) ATP poison ArBS-K/G Water PBS-K/G
DCCD (10 μM) F0F1 ATPase inhibitor PBS/G EtOH (0.025) PBS/G + 0.025% EtOH
Sodium orthovanadate (1 mM) P-type ATPase inhibitor PBS-K/G Water PBS-K/G
Phenamil (10 μM) Sodium channel blocker PBS/G MeOH (0.1) PBS/G + 0.1% MeOH
Amiloride (10 μM) Sodium channel blocker PBS/G Water PBS/G
Rifampin (5 μg/ml) RNA synthesis inhibitor PBS/G MeOH (0.1) PBS/G + 0.1% MeOH
Puromycin (20 μM) Protein translation inhibitor PBS/G Water PBS/G
a

Stock solutions were made of the test substance (for non-water-soluble compounds) in the solvent listed. The stock solution was then added to the base buffer, resulting in the final solvent concentration shown, where applicable. Abbreviations: MeOH, methanol; EtOH, ethanol.