J. Chromatogr. A 731, 293-298 (1996). Presentation of a staining techniques for glucose oxidase activity on polyacrylamide gels, based on the fact that glucose oxidase reacts with one-electron scavengers in a reaction dependent on pH and pO2. Demonstration of reduction of ferricyanide, cuprisulfate, ferrycytochrome C and nitrotetrazolium blue reduction leading to sharp colored bands under aerobic conditions. Comparison with conventional peroxidase/O-dianisidine-assay.

J. Neurochem. 44, 370-375 (1985). Assay for microsomal alkenylhydrolyse activity of rat brain. Free aldehydes are formed in this enzymatic reaction. The analysis is based on a known TLC method for fragments of plasmalogens using silica or cellulose and chloroform - methanol - water 3:7:3. Detection with iodine vapors and/or ninhydrin, scintillation counting.

Biom. Chromatogr. 10, 97-98 (1996). Electrophoresis on 0.75 mm gels of 10% polyacrylamide. Immunodetection by using rabbit anti LPO antibodies (30mg/mL), peroxidase-anti-peroxidase soluble complex and diamino-benzidine tetrahydrochloride. Discussion of the merits of the improved procedure.

J. Neurochem. 44, 411-420 (1985). The known procedure of peptide mapping after tryptic fragmentation is performed 2-dimensionally by TLC on silica with propanol -34 % NH3 7:3, followed by TLE at pH 3.5, 800 V, 50 minutes with acetic acid - pyridine - water 10:1:300. The peptides are sprayed with fluorescamine, followed by triethylamine treatment, then visualized by UV.

J. Chromatogr. A 743, 105-122 (1996). A review with 113 references on the historical development of ACE purifaction and assay methods, including SDS-PAGE with direct radioimmunoassay, or immune isolation with quantification by SDS-PAGE, and HPLC, etc.

Experientia 41, 485-486 (1985). TLC of the 2, 4-dinitrophenylhydrazones of 1-gulonolacetone, l-ascorbic acid and other derivatives produced by enzymatic reaction on silica with ethyl acetate - chloroform - acetic acid - acetone 70:50:7:6. Comparison with authentic identification standards.

J. Chin. Trad. Med. (Zhongguo Zhongyao Zazhi) 22, 325-326 (1997). IEFE on polyacrylamide gel layer at 4°C. Separation of malate dehydrogenase isozyme bands for the sample from the tissues of fowl.

Biochem. Biophys. Res. Commun. 378, 224-229 (2009). TLC of the hydrolytic action patterns of the purified Nostoc punctiforme debranching enzyme on the following substrates: pullulan, amylopectin, soluble starch, amylose, cyclodextrins, and maltooligosaccharides (form glucose to maltoheptaose), on silica gel with 1-propyl alcohol – ethyl acetate – water 6:2:3. Detection by dipping into 0.3 % N-(1-naphthyl)-ethylenediamine and 5 % sulfuric acid in methanol, followed by heating for 10 min at 110 °C. Quantitative determination by radioactivity measurement of the 14C-labeled maltooligosaccharides.