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JJ Edwards, NG Anderson, SL Nance and NL Anderson
Human erythrocyte lysate proteins were resolved into over 250 discrete
spots by two-dimensional electrophoresis using isoelectric focusing in the
first dimension and electrophoresis in the presence of sodium dodecyl
sulfate, (SDS) in the second. The overwhelming excess of hemoglobin has
made such analyses difficult in the past. However, with the ISO-DALT
two-dimensional electrophoresis system, large numbers of red cell proteins
can be mapped in the presence of hemoglobin. When hemoglobin and several
other major proteins are removed by adsorption to DEAE-cellulose,
additional minor components are seen, giving a total of over 275. With the
use of purified preparations, the map positions of five cell enzymes or
their subunits were determined: pyruvate kinase, catalase,
glucose-6-phosphate dehydrogenase, hypoxanthine phosphoribosyltransferase,
and carbonic anhydrase. The mapping techniques described complement and
extend those traditionally used to find human red cell protein variants.
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| Copyright © 1979 by American Society of Hematology Online ISSN: 1528-0020 | |||||||||