Abstract
IN the course of a survey of Gold Coast Africans1, one individual was discovered who had both normal hæmoglobin and one hitherto not known which was designated as hæmoglobin G 2. Hæmoglobin G was found to differ from all other known hæmoglobins in its mobility on paper electrophoresis at pH 8.6 (veronal buffer). The hæmoglobins most similar in mobility were sickle-cell hæmoglobin (S), fœtal hæmoglobin (F) and hæmoglobin D. S could in addition be differentiated by its low solubility when in the reduced state, and F by its resistance towards denaturation by alkali. For the distinction from hæmoglobin D, reliance had to be placed on the reported mobility of the latter, which was exactly that of S in open-boundary electrophoresis at acid and at alkaline pH3. Further steps have now been taken to establish the properties of hæmoglobin G.
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References
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EDINGTON, G., LEHMANN, H. & SCHNEIDER, R. Characterization and Genetics of Hæmoglobin G . Nature 175, 850–851 (1955). https://doi.org/10.1038/175850a0
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DOI: https://doi.org/10.1038/175850a0
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