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- W2012015752 abstract "I. Lactic dehydrogenase isoenzymes can be separated by column chromatography on Sephadex-DEAE ®. Electrophoretically slow migrating isoenzymes are not absorbed at an ionic strength of less than 0.05 at pH 7.5. By increasing the ionic strength the different isoenzymes can be eluted in the order of their electrophoretic migration. 2. A rapid and simple method for the assay of LDH isoenzymes in mixtures (serum, homogenates) using Sephadex-DEAE in an adsorption-elution type technique is described. Four isoenzymes are differentiated. 3. Human tissues were assayed for their isoenzyme patterns. Tissues with high aerobic metabolism (cardiac muscle, brain, kidney) have a high content of electrophoretically fast moving isoenzymes. Electrophoretically slow moving isoenzymes predominate in skeletal muscle, amnion, synovial tissue and liver. 4. It is shown that lactic dehydrogenase activity in homogenates is much higher if the isoenzymes are separated prior to assay. Enzyme determinations in homogenates may give results which correspond to less than half the true enzyme activities." @default.
- W2012015752 created "2016-06-24" @default.
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- W2012015752 date "1963-03-01" @default.
- W2012015752 modified "2023-09-24" @default.
- W2012015752 title "A study of lactic dehydrogenase isoenzyme pattern of human tissues by adsorptionelution on Sephadex-DEAE" @default.
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- W2012015752 doi "https://doi.org/10.1016/0009-8981(63)90155-4" @default.
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