Ellmans Reagent

Ellmans Reagent

Published on 03/12/2013

DTNB, frequently called Ellman’s Reagent, used as reagent for determination of free sulfhydryl groups.



DTNB, frequently called Ellman’s Reagent, used as reagent for determination of free sulfhydryl groups. Through reaction with aliphatic thiol groups a mixed disulfide of protein thiol and one mole of 2-nitro-5-thiobenzoate per mole of protein sulfhydryl group is being formed. DTNB has little absorbance. Reaction with -SH groups on proteins (from any solvent accessible Cys) under mild alkaline conditions (pH 7-8) produces the 2-nitro-5-thiobenzoate anion, which gives an intense yellow color with an absorption maximum at 409.5 nm (Extinction coefficient: 14150 M -1*cm -1). Ellman’s reagent is sensitive to various buffer ions, therefore, the extinction coefficient used to calculate the number of sulfhydryl groups must be matched to the reaction conditions. In case the thiol groups are in disulfide bonds, they must be reduced under anaerobic conditions prior to reaction with DTNB. 
Solubility 8 mg/mL in EtOH. Stock solutions c an be prepared in 0.1 M phosphate buffer, which are stable over several weeks.



References:

  • Ellman, G.L., Arch. Biochem. Biophys. 1959; 82: 70.
  • Gething, M.J. and Davidson, B.E., Eur. J.Biochem. 1972; 30: 352.
  • Habeeb, A.F.S.A., Methods in Enzymology1972; 25: 457.
  • Ellman, G.L., Arch. Biochem. Biophys. 1958; 74: 443.
  • Riddles, P.W. et al., Anal. Biochem. 1979; 94: 75.
  • Ming, D. et al., Biotechniques1995; 18: 808.
  • Robyt, J.F. et al., Arch. Biochem. Biophys. 1971; 147: 262.
  • Brockelhurst, K. et al, Biochem. J. 1972; 811-816.
  • McKelvy, J.F. et al., Arch. Biochem. Biophys. 1969; 132: 99-110.
  • Anderson, W.L. et al., Anal. Biochem. 1975; 67: 493.
  • Nashef, A.S. et al., Anal. Biochem. 1977; 79: 394-405.
  • Kuwata, K. et al., Anal. Chem. 1982; 54: 1082.
  • Harrap, K.R., Biochem. Pharmacol. 1967; 16: 725-731.
  • Bode, J., Anal. Biochem. 1979; 94: 465-469.
  • Palau, J., Biochim. Biophys. Acta 1978; 536: 323-327.
  • Danehy, J.P, Elia, V.J. and Lavelle, C.J., J. Org. Chem. 1971; 36: 1003.