The objective of this study has been to determine which Na,K-ATPase isoforms are expressed in red blood cells and whether kinetic differences in the uncoupled sodium eff lux mode between the human red blood cell Na,KATPase and other preparations can be explained by differences in the underlying subunit composition. To this end, human reticulocyte RNA was isolated, reverse transcribed, amplified by PCR and appropriate primers, and sequenced. Primers from highly conserved areas as well as isoformspecific primers were used. The ␣1 and ␣3 isoforms of the ␣ subunit, and the 2 and 3 isoforms of the  subunit were found. The complete coding regions of the cDNAs for the reticulocyte subunits were sequenced from overlapping PCR fragments. No difference was found between the reticulocyte isoforms and the ones already known. The fact that we found 2 but not 1 in reticulocyte single-stranded cDNA, and 1 but not 2 in a leukocyte library indicates that leukocyte contamination of our reticulocyte preparation was negligible. Analysis of a human bone marrow library showed that ␣1, ␣2, and ␣3 as well as all three  isoforms were present. The extent to which the kinetic properties of uncoupled sodium eff lux might depend on different isoform combinations is not yet known.