1958
DOI: 10.1016/0006-3002(58)90201-4
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A method for the determination of insulin by paper chromatography

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1959
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Cited by 10 publications
(4 citation statements)
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“…20/150 filter paper 8 with the organic phase of a 3:1:4 mixture of n-butanol:acetic acid:water. 9 This system was chosen on the basis of its ability to resolve the components of a mixture consisting of insulin, 3-iodotyrosine, 3,5-diiodotyrosine, and inorganic iodide. No evidence has been found for the lability of organically bound iodine in this system.…”
Section: Methodsmentioning
confidence: 99%
“…20/150 filter paper 8 with the organic phase of a 3:1:4 mixture of n-butanol:acetic acid:water. 9 This system was chosen on the basis of its ability to resolve the components of a mixture consisting of insulin, 3-iodotyrosine, 3,5-diiodotyrosine, and inorganic iodide. No evidence has been found for the lability of organically bound iodine in this system.…”
Section: Methodsmentioning
confidence: 99%
“…The Latin-square design balanced out positional and paper effects, since each spot of test and standard occurred once on each paper and occupied all available positions over the four papers. Several unsuccessful attempts were made to separate insulin from crystalline glucagon (Staub, Sinn & Behrens, 1953, by the chromatographic method as described and by the radial technique of Bouman & Homan (1958). Although the latter procedure gave somewhat better separation in our hands than the ascending method, there was still some overlapping of the spots.…”
Section: Resultsmentioning
confidence: 80%
“…The co-ordinate values, after transformation to logarithms to base 10, gave X = 1.08 Y 0 12 and Y = 0 885X 0 173 for the best-fitting lines. (Fenton, 1959) and temperature fluctuations (Bouman & Homan, 1958). These effects had to be compensated by the presence of standards on every paper in each assay.…”
Section: Resultsmentioning
confidence: 99%
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