1967
DOI: 10.1016/0009-8981(67)90330-0
|View full text |Cite
|
Sign up to set email alerts
|

Quantitative assay of lactate dehydrogenase isoenzymes by reflectance densitometry

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1

Citation Types

0
4
0

Year Published

1968
1968
1980
1980

Publication Types

Select...
9

Relationship

1
8

Authors

Journals

citations
Cited by 14 publications
(4 citation statements)
references
References 7 publications
0
4
0
Order By: Relevance
“…The percentage M sub-unit contribution to the LDH isoenzyme patterns of the cultured explants was estimated quantitatively following vertical starch gel electrophoresis by reflectance densitometry according to the method of Latner and Turner (1967).…”
Section: Methodsmentioning
confidence: 99%
“…The percentage M sub-unit contribution to the LDH isoenzyme patterns of the cultured explants was estimated quantitatively following vertical starch gel electrophoresis by reflectance densitometry according to the method of Latner and Turner (1967).…”
Section: Methodsmentioning
confidence: 99%
“…Lactate dehydrogenase isoenzymes were estimated by reflectance densitometry (Latner and Turner, 1967) after separation by starch gel electrophoresis (Smithies, 1959) in Tris-borate-EDTA buffers, pH 8.6, (Boyer et ul, 1963) and staining by a method essentially that of Latner and Skillen (1961). The proportions of the two subunits were calculated from the known tetrameric structure of the five types of isoenzyme molecule present in most tissues (Shaw and Barto, 1963).…”
Section: Enzyme Assaymentioning
confidence: 99%
“…The resolution power in starch is higher than that in agarose [27,53,54,55], but the quantitative evaluation of isoenzyme activities, when performed by reflectance densitometry, is more readily performed in agarose than in starch gels. Moreover, the results obtained from agarose are easier to reproduce than those from starch gels, provided that the recommendations given by Latner and T urner [29] are followed. In some analyses in the present investigation, however, too intense colour was obtained in the LDj to give a relevant measure of the activity of the corresponding isoenzyme.…”
Section: Demonstration Of the Isoenzymes Of Ldh And Mdh By Zone Electmentioning
confidence: 99%