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08U/mg, 21.74U/mg, and 14.18U/mg, respectively. There was a desirable linear correlation between the activities of recombinant LDH isoenzymes and their protein concentrations. Electrophoresis of LDH isoenzymes showed that the recombinant LDH-B corresponded to LDH1 and it demonstrated good stability at 4°C and 25°C for 5weeks. LDH-B formulations in saline-bovine serum albumin solution and human serum matrix were commutable for six routine methods. Human recombinant LDH-B has great potential to become an improved and less expensive
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