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Journal Abstract Search

123 related items for PubMed ID: 231392

  • 1. Phenazine ethosulfate as a preferred electron acceptor to phenazine methosulfate in dye-linked enzyme assays.
    Ghosh R, Quayle JR.
    Anal Biochem; 1979 Oct 15; 99(1):112-7. PubMed ID: 231392
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  • 3. Understanding the chemistry of the artificial electron acceptors PES, PMS, DCPIP and Wurster's Blue in methanol dehydrogenase assays.
    Jahn B, Jonasson NSW, Hu H, Singer H, Pol A, Good NM, den Camp HJMO, Martinez-Gomez NC, Daumann LJ.
    J Biol Inorg Chem; 2020 Mar 15; 25(2):199-212. PubMed ID: 32060650
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  • 7. A partial kinetic analysis of the chemiluminescence (CL) of phenazine methosulfate (PMS).
    STEELE RH, BRECKINRIDGE BS.
    Biochem Biophys Res Commun; 1963 Mar 05; 10():396-400. PubMed ID: 13983575
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  • 8. Site of interaction between phenazine methosulphate and the respiratory chain of Bacillus subtilis.
    Bisschop A, Bergsma J, Konings WN.
    Eur J Biochem; 1979 Jan 15; 93(2):369-74. PubMed ID: 218814
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  • 9. Free radical production from the aerobic oxidation of reduced pyridine nucleotides catalysed by phenazine derivatives.
    Davis G, Thornalley PJ.
    Biochim Biophys Acta; 1983 Sep 30; 724(3):456-64. PubMed ID: 6311259
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  • 10. Aerobic denitration of 2,4,6-trinitrotoluene in the presence of phenazine compounds and reduced pyridine nucleotides.
    Stenuit B, Lamblin G, Cornelis P, Agathos SN.
    Environ Sci Technol; 2012 Oct 02; 46(19):10605-13. PubMed ID: 22881832
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  • 11. Care in use of phenazine methosulfate in the laboratory.
    Worsfold M.
    Clin Chem; 1980 Oct 02; 26(11):1622. PubMed ID: 6158386
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  • 12. Intermediate electron-acceptors in quantitative cytochemistry. Comparison of phenazine methosulphate and Meldola Blue.
    Henderson B, Loveridge N.
    Histochemistry; 1981 Oct 02; 72(4):617-23. PubMed ID: 7298392
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  • 19. Care in use of phenazine methosulfate in the laboratory.
    Jacobson D.
    Clin Chem; 1979 Oct 02; 25(10):1963-4. PubMed ID: 476952
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  • 20. A chemiluminescence (CL) of phenazine methosulfate (PMS) in the presence of hydrogen peroxide (HOOH) induced by reductants including reduced nicotinamide adenine dinucleotide (NADH) and ascorbic acid (AA).
    CHAYET C, STEELE RH, BRECKINRIDGE BS.
    Biochem Biophys Res Commun; 1963 Mar 05; 10():390-5. PubMed ID: 14040658
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