1972
DOI: 10.1093/clinchem/18.5.489
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Sickle-Cell Anemia: A Simplified Screening Procedure

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“…The erythrocytes were separated by centrifugation for 15 min at 482 g. The plasma portions were removed by aspiration and the packed cells were washed with isotonic phosphate buffer (310 imOsm) solution (PBS)* and centrifuged as before. The phenotypes of all erythrocyte samples were separately determined by microelectrophoresis technique on cellulose acetate (8,9) and confirmed by immunoprecipitation * Buffer mixtures: 2 separate phosphate buffer solutions were prepared as follows: 0.155 mol/l (310 ideal milliosmolar) sodium phosphate monobasic (NaH2P04) and 0.103 mol/l (310 ideal milliosmolar) sodium phosphate dibasic (Na2HP04). Isotonic phosphate buffers were prepared at pH 7.4 and 8.2 by mixing appropriate ratios of the stock solutions according to Henderson-Hasselbalch equation.…”
mentioning
confidence: 99%
“…The erythrocytes were separated by centrifugation for 15 min at 482 g. The plasma portions were removed by aspiration and the packed cells were washed with isotonic phosphate buffer (310 imOsm) solution (PBS)* and centrifuged as before. The phenotypes of all erythrocyte samples were separately determined by microelectrophoresis technique on cellulose acetate (8,9) and confirmed by immunoprecipitation * Buffer mixtures: 2 separate phosphate buffer solutions were prepared as follows: 0.155 mol/l (310 ideal milliosmolar) sodium phosphate monobasic (NaH2P04) and 0.103 mol/l (310 ideal milliosmolar) sodium phosphate dibasic (Na2HP04). Isotonic phosphate buffers were prepared at pH 7.4 and 8.2 by mixing appropriate ratios of the stock solutions according to Henderson-Hasselbalch equation.…”
mentioning
confidence: 99%