Add washed RBC of HbA or HbS or HbA+HBS EDTA sample in 2 ml CPDA bottle till total volume become 4 ml approximately.
Use washed RBC to prevent mismatch agglutination in pooled RBC
Wash with saline twice in 4 ml EDTA vacumm tube. Remove Saline part
After washing,Add Preservative CPDA in washed RBCs in 1:1 ratio.
Prepare aliquots of 50 ul.
Label and store at 2-8'C.