Materials with blood group activity A, B and H have been obtained from
erythrocyte stroma by phenol extraction and subsequent purification by chromatography
on Sephadex G-200 and ultracentrifugation at 180,000 g for 4 h.
The final materials contain carbohydrates, protein and lipids, have a specific activity
similar to that of the glycolipids extracted from erythrocyte stroma by other workers,
and are found not to be homogeneous on ultracentrifugal analysis. Treatment with 0.5%
SDS results in the reduction of the average particle size and in the appearance of new
units which sediment homogeneously.
However, in the presence of SDS the greatest part of the specific activity is lost, while
extraction with butanol drastically reduces the At specific activity and to some extent the
B activity has no influence on the A and probably none on the H activity.
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