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METHOD FOR ANALYSING AND DETERMINING THE METABOLIC STATE OF TRACE ELEMENTS IN MAMMALS, BASED ON THE PROTEIN PROFILE ASSOCIATED WITH A SUPRA-NUTRITIONAL METABOLIC STATE OF THE TRACE ELEMENTS AND THE PROTEIN PATTERN
METHOD FOR ANALYSING AND DETERMINING THE METABOLIC STATE OF TRACE ELEMENTS IN MAMMALS, BASED ON THE PROTEIN PROFILE ASSOCIATED WITH A SUPRA-NUTRITIONAL METABOLIC STATE OF THE TRACE ELEMENTS AND THE PROTEIN PATTERN
The invention relates to an electrophoretic protein pattern for determining the metabolic state of trace elements, particularly selenium since it comprises at least one plasma protein corresponding to an internal peptide of the complement of the inhibitory factor, represented by band R-3 and, optionally, one or all of the internal peptides represented by bands R-2 and R4 to R15, wherein band R-2 is protein complement inhibitor factor H, band R-3 is complement inhibitor factor H, band R-4 is plasminogen isoform CRA_f, band R-5 is protein LOC366747, band R-6 is complement component 4a, band R-7 is albumin, band R-8 is Dal-24, R-9 is Ig Gamma- 2C chain C region, band R-10 is β-2-glycoprotein 1 precursor, band R-11 is Ig Gamma-2A chain region C, band R-12 is complement component 4a, band R-13 is inter-α-inhibitor heavy chain H4, band R-14 is Ig kappa precursor, band R-15 is Apolipoprotein H, said bands being obtained by means of electrophoretic fractionation of plasma proteins of basic isoelectric point. The invention also relates to the method for analysing and determining the metabolic state of trace elements in mammals.
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