Adsorbentes de afinidad para plasminógeno

Uso de un adsorbente de afinidad para la separación, eliminación, aislamiento, purificación, caracterización, identificación o cuantificación de un plasminógeno o una proteína que es un análogo del plasminógeno, donde el adsorbente de afinidad es un compuesto de fórmula III, IV o V: **Fórmula** dond...

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Hauptverfasser: KUHN, Claudia, PEARSON, James, BETLEY, Jason, BAINES, Baldev
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creator KUHN, Claudia
PEARSON, James
BETLEY, Jason
BAINES, Baldev
description Uso de un adsorbente de afinidad para la separación, eliminación, aislamiento, purificación, caracterización, identificación o cuantificación de un plasminógeno o una proteína que es un análogo del plasminógeno, donde el adsorbente de afinidad es un compuesto de fórmula III, IV o V: **Fórmula** donde A es una matriz de soporte, unida opcionalmente al anillo triazina por un espaciador. For the separation, removal, isolation, purification, characterization, identification or quantification of plasminogen or a protein that is a plasminogen analogue, an affinity adsorbent is used that is a compound of formula (II) wherein one X is N and the other is N, C-Cl or C-CN; A is a support matrix, optionally linked to the triazine ring by a spacer; Z is O, S or N-R and R is H, C1-6 alkyl, C1-6 hydroxyalkyl, benzyl or -phenylethyl; B is an optionally substituted hydrocarbon linkage containing from 1 to 10 carbon atoms; D is H, OH or a primary amino, secondary amino, tertiary amino, quaternary ammonium, imidazole, guanidino or amidino group; or B-D is -CHCOOH-(CH2)3-4-NH2; and q is 2 to 6.
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For the separation, removal, isolation, purification, characterization, identification or quantification of plasminogen or a protein that is a plasminogen analogue, an affinity adsorbent is used that is a compound of formula (II) wherein one X is N and the other is N, C-Cl or C-CN; A is a support matrix, optionally linked to the triazine ring by a spacer; Z is O, S or N-R and R is H, C1-6 alkyl, C1-6 hydroxyalkyl, benzyl or -phenylethyl; B is an optionally substituted hydrocarbon linkage containing from 1 to 10 carbon atoms; D is H, OH or a primary amino, secondary amino, tertiary amino, quaternary ammonium, imidazole, guanidino or amidino group; or B-D is -CHCOOH-(CH2)3-4-NH2; and q is 2 to 6.</abstract><oa>free_for_read</oa></addata></record>
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subjects BEER
BIOCHEMISTRY
CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOIDCHEMISTRY
CHEMISTRY
COMPOSITIONS OR TEST PAPERS THEREFOR
CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL ORENZYMOLOGICAL PROCESSES
ENZYMOLOGY
HETEROCYCLIC COMPOUNDS
INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIRCHEMICAL OR PHYSICAL PROPERTIES
MEASURING
MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEICACIDS OR MICROORGANISMS
METALLURGY
MICROBIOLOGY
MUTATION OR GENETIC ENGINEERING
ORGANIC CHEMISTRY
PERFORMING OPERATIONS
PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
PHYSICS
PROCESSES OF PREPARING SUCH COMPOSITIONS
SPIRITS
TESTING
THEIR RELEVANT APPARATUS
TRANSPORTING
VINEGAR
WINE
title Adsorbentes de afinidad para plasminógeno
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