Improved column method for separating lactate dehydrogenase isoenzymes 1 and 2.

Abstract:

:Lactate dehydrogenase (LD) isoenzymes 1 and 2 in human serum were separated on a column of diethylaminoethyl-Sephadex. Samples layered on mini-columns were eluted with buffered sodium chloride (100, 150, and 200 mmol/liter). Lactate dehydrogenase activity in column effluents was measured by the Wacker method, and their isoenzyme content was evaluated by electrophoresis on polyacrylamide gel. Results for column-fractionated LD-1 and LD-2 were expressed in two ways: LD-1/LD-2 ratios and total LD-1 + LD-2 activities. The former is a more specific indicator of myocardial infarction than the latter. Sera from 10 patients with acute myocardial infarction (increased creatine kinease isoenzyme MB activity) exhibited ratios in the range of 0.92 to 1.56, ratios for 10 patients without heart disease (normal creatine kinase MB) ranged from 0.33 to 0.69.

journal_name

Clin Chem

journal_title

Clinical chemistry

authors

Mercer DW

subject

Has Abstract

pub_date

1978-03-01 00:00:00

pages

480-2

issue

3

eissn

0009-9147

issn

1530-8561

journal_volume

24

pub_type

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