1972
DOI: 10.1139/f72-172
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Amine-Citrate Buffers for pH Control in Starch Gel Electrophoresis

Abstract: Amine-citrate buffer systems for pH control in starch gel electrophoresis gave good resolution of some dehydrogenase isozymes. The pK's of three new amine buffers, N-(3-aminopropyl)-morpholine, pK2 25 C, 6.12; N-(3-aminopropyl)-diethanolamine, pK2 25 C, 6.90; and 1,3-bis(dimethylamino)-2-propanol, pK2 25 C, 7.55, were determined at 5 C intervals in the range 10–40 C. These compounds, together with N, N-bis(2-hydroxyethyl)iminotris(hydroxymethyl)methane (bis-Tris) and tris-(hydroxymethyl)-methylamine(Tris), pro… Show more

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Cited by 958 publications
(323 citation statements)
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“…Eight enzyme systems showed simple banding patterns and could be reliably scored: phosphoglucomutase (PGM, EC 5.4.2.2), uridine diphosphoglucose pyrophosphorylase (UGPP, EC 2.7.7.9), aconitate hydratase (ACO, EC 4.2.1.3), isocitrate dehydrogenase (IDH, EC 1.1.1.41), glucose-6-phosphate isomerase (GPI, EC 5.3.1.9), triose-phosphate isomerase (TPI, EC 5.3.1.1), 6-phosphogluconic dehydrogenase (6PG, EC 1.1.1.44), and aspartate aminotransferase (GOT EC 2.6.1.1). Phosphoglucomutase, UGPP, ACO, IDH, and 6PG were resolved on a morpholine citrate buffer system at pH 7.8 (Clayton & Tretiak 1972). Glucose-6-phosphate isomerase, GOT, and TPI were assayed on a lithium borate buffer at pH 8.3 (Soltis et al 1983).…”
Section: Methodsmentioning
confidence: 99%
“…Eight enzyme systems showed simple banding patterns and could be reliably scored: phosphoglucomutase (PGM, EC 5.4.2.2), uridine diphosphoglucose pyrophosphorylase (UGPP, EC 2.7.7.9), aconitate hydratase (ACO, EC 4.2.1.3), isocitrate dehydrogenase (IDH, EC 1.1.1.41), glucose-6-phosphate isomerase (GPI, EC 5.3.1.9), triose-phosphate isomerase (TPI, EC 5.3.1.1), 6-phosphogluconic dehydrogenase (6PG, EC 1.1.1.44), and aspartate aminotransferase (GOT EC 2.6.1.1). Phosphoglucomutase, UGPP, ACO, IDH, and 6PG were resolved on a morpholine citrate buffer system at pH 7.8 (Clayton & Tretiak 1972). Glucose-6-phosphate isomerase, GOT, and TPI were assayed on a lithium borate buffer at pH 8.3 (Soltis et al 1983).…”
Section: Methodsmentioning
confidence: 99%
“…Described by Clayton and Tretiak (1972) The recipes for general protein and specific enzyme stains have been adapted from Allendorf et a!., (1977), Manlove et aL, (1975), Harris and Hopkinson (1976), and Gyllensten et a!., (1980). The following 24 proteins were examined (enzyme abbreviation, buffer system (1-4), type of tissue (M = muscle, K = kidney, S = blood serum) and enzyme commission (EC) nomenclature in parenthesis): Acid phosphatase (AP, 3, M, EC 3.…”
Section: Methodsmentioning
confidence: 99%
“…The following six loci were studied: AAT4*, IDPH3*, MDH3,4*, mMEP2*, IDDH-1 * and IDDH2*. Two buffer systems were used in the electrophoretic analysis; a continuous citrate-aminopropylmorpholine system (Clayton & Tretiak, 1972) for 5AAT4*, IDPH3*, MDH3,4* and mMEP2*, and a discontinuous Tris-citrate-borate system (Ridgway et a!., 1970) for IDDH1* and IDDH2*. Specific staining for enzymes was carried out using the methods of Cross & Ward (1980) and Aebersold et a!.…”
Section: Protein Analysismentioning
confidence: 99%