|
|
||||||||
Clinical Chemistry, Vol 17, 290-295, Copyright © 1971 by the American Association for Clinical Chemistry
1 Bio-Science Laboratories, 7600 Tyrone Ave., Van Nuys,
Calif. 91405.
An electrophoretic method is presented for separating alkaline phosphatase
isoenzymes on agarose gel by using barbital buffer.
-Naphthyl AS-MX
phosphate was converted to the highly fluorescent
-naphthol AS-MX, to
detect the zones of enzymic activity on the thin film. The fluorescent zones
on the electropherograms were scanned with a recording fluorometer and
the electrophoretic mobilities of the enzymes were compared with those of
the plasma proteins. This method was used to assess the isoenzyme
patterns in human sera and tissues (liver, bone, kidney, spleen, and placenta).
-naphthyl AS-MX phosphate fluorometry isoenzymes in human sera and tissues, normal patterns and values
Submitted on December 9, 1970
Accepted on January 15, 1971
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |