Polymorphism of erythrocyte acid phosphatase and adenosindesaminase in Galicia (N.W. Spain) by AGIF and PAGIF

Carracedo, Ángel; Concheiro, L.

doi:10.1007/bf00200747

Cited by 3 publications

(2 citation statements)

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“…Table 7 shows the a priori exclusion rate of all systems which were used in our laboratory, classified in descending order of exclusion efficiency. This order A. Carracedo and L. Concheiro [15] A. Carracedo and J. L. Blazquez [16] This paper A. Carracedo and L. Concheiro [14] A. Carracedo and L. Concheiro [15] A. Carracedo and L. Concheiro [14] A. Carracedo and J. L. Blazquez [16] This paper C. Llano [18] C. Llano [18] C. Llano [18] In addition, accepting _ 1 difference in verbal predicates, the above-mentioned tables can be used with most European populations, although the agreement for the Galician population is not perfect (99%).…”

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confidence: 95%

Plasma protein and red cell enzyme groups in Galicia (North West Spain)

et al. 1987

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Galactose-1-phosphate uridyl transferase (GALT), esterase D (EsD), and plasminogen (PLG) phenotypes were determined by isoelectric focusing in thin-layer polyacrylamide gels (PAGIF) in a random sample from Galicia. Haptoglobins (Hp) were determined by conventional electrophoresis. The following gene frequencies were observed: for GALT: GALTN: 0.930; GALTD1: 0.044; GALTD2: 0.025; for EsD: EsD1: 0.874; EsD2: 0.104; EsD3: 0.021; for PLG: PLG1: 0.800; PLG2: 0.199; for Hp: Hp1: 0.426; Hp2: 0.573. Population data results of all electrophoretic markers typed until now in Galician population are also included.

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confidence: 95%

Plasma protein and red cell enzyme groups in Galicia (North West Spain)

et al. 1987

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“…Recently, isoelectric focusing has been introduced for the analysis of ACP1 isoenzymes because of the high resolution capacity (Burdett and Whitehead 1977;Randall et al 1980;Divall 1981;Carracedo and Concheiro 1982;Dorrill and Sutton 1983;Budowle 1984;Westwood and Sutton 1984;Finney et al 1985;Yuasa et al 1985;Frank and Stolorow 1986). Using this technique some of the above workers phenotyped ACP1 from bloodstains and these ranged in age from 2 weeks to 1 year (Randall et al 1980;Dorrill and Sutton 1983;Westwood and Sutton 1984;Frank and Stolorow 1986).…”

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Polymorphism of ACP1 by isoelectric focusing : Population study in Japanese and phenotyping in bloodstains.

Komatsu

Kido

Oya

1987

Tohoku J. Exp. Med.

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A. and OYA, M. Polymorphism of ACPI by Isoelectric Focusing : Population Study in Japanese and Phenotyping in Bloodstains. Tohoku J. exp. Med., 1987, 151(3), 317-321 The polymorphism of ACP1 was investigated in 749 unrelated Japanese individuals by isoelectric focusing. The allele frequencies were A CPl *A =0.2083 and ACPI * B = 0.7917, which were almost similar to those reported in other Japanese subpopulations. The isoelectric focusing technique was successfully applied to ACPI typing in bloodstains ; each phenotype was demonstrated at 37°C for up to 4 weeks, at room temperature for up to 10 weeks and at 4°C for over 16 weeks after stain formation. The isoelectric focusing method proved more useful than conventional electrophoretic methods in medicolegal practice. enzyme polymorphism ; isoelectric focusing ; ACP1 types ; population study in Japanese ; grouping of bloodstains Since the discovery of ACP1 polymorphism by Hopkinson et al. (1963), a large number of works have been performed using starch, agarose or cellulose acetate electrophoresis, and this system is now an accepted genetic marker for paternity testing and blood individualization.Recently, isoelectric focusing has been introduced for the analysis of ACP1 isoenzymes because of the high resolution capacity

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