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Characterization and Genetics of Hæmoglobin G
IN the course of a survey of Gold Coast Africans 1 , 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 p H 8.6...
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Published in: | Nature (London) 1955-05, Vol.175 (4463), p.850-851 |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | IN the course of a survey of Gold Coast Africans
1
, 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
p
H 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
p
H
3
. Further steps have now been taken to establish the properties of hæmoglobin
G
. |
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ISSN: | 0028-0836 1476-4687 |
DOI: | 10.1038/175850a0 |