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Problems associated with the assay of arylsulphatases A and B of rat tissues
A method for the separation and purification of rat liver arylsulphatases A and B by gel filtration on Sephadex G-200 is described. The properties of the A enzyme and its molecular weight are similar to those of the corresponding ox liver enzyme. The B enzymes were found to be dissimilar. The method...
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Published in: | Biochemical journal 1973-05, Vol.134 (1), p.183-190 |
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container_title | Biochemical journal |
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creator | Worwood, M Dodgson, K S Hook, G E Rose, F A |
description | A method for the separation and purification of rat liver arylsulphatases A and B by gel filtration on Sephadex G-200 is described. The properties of the A enzyme and its molecular weight are similar to those of the corresponding ox liver enzyme. The B enzymes were found to be dissimilar. The method already developed for the assay of the corresponding enzymes from human tissues was shown to be unsuitable for the assay of the enzymes of rat tissues. A method of assay was developed which permits an approximate determination of the individual rat liver enzymes in a mixture of the two, but precise determination requires prior separation of the enzymes by gel-filtration chromatography. |
doi_str_mv | 10.1042/bj1340183 |
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A method of assay was developed which permits an approximate determination of the individual rat liver enzymes in a mixture of the two, but precise determination requires prior separation of the enzymes by gel-filtration chromatography.</description><subject>Animals</subject><subject>Cellular Interactions and Control Processes</subject><subject>Chromatography, Gel</subject><subject>Chromatography, Ion Exchange</subject><subject>Hydrogen-Ion Concentration</subject><subject>Kinetics</subject><subject>Liver - enzymology</subject><subject>Methods</subject><subject>Molecular Weight</subject><subject>Nitrophenols</subject><subject>Rats</subject><subject>Sulfatases - analysis</subject><subject>Sulfatases - isolation & purification</subject><subject>Temperature</subject><subject>Time Factors</subject><issn>0264-6021</issn><issn>0306-3283</issn><issn>1470-8728</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1973</creationdate><recordtype>article</recordtype><recordid>eNpVkEtLw0AUhQdRaq0u_AHCrAQX0TuPZCYbQYsvKOhC18NNcmNS8qiZROm_N6Wl6OrCOR_nHg5j5wKuBWh5kyyF0iCsOmBToQ0E1kh7yKYgIx1EIMUxO_F-CSA0aJiwiTZSSQlTtnjr2qSi2nP0vk1L7CnjP2Vf8L6gjYZr3uYcu3Xlh2pVYI-ePL_j2GT8fmN12PO-9H4gf8qOcqw8ne3ujH08PrzPn4PF69PL_G4RpNKGKhBhbsMstFmeW0xDkqEhYyxZQptLBTHEuZSaFESJlJiiiNGYTKqYACxqNWO329zVkNSUpdT0HVZu1ZX1WNS1WLr_TlMW7rP9dkIYY2I7BlzuArr2ayzeu7r0KVUVNtQO3lkR20iFMIJXWzDtWu87yvdPBLjN9G4__che_G21J3dbq19rDH7o</recordid><startdate>19730501</startdate><enddate>19730501</enddate><creator>Worwood, M</creator><creator>Dodgson, K S</creator><creator>Hook, G E</creator><creator>Rose, F A</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19730501</creationdate><title>Problems associated with the assay of arylsulphatases A and B of rat tissues</title><author>Worwood, M ; Dodgson, K S ; Hook, G E ; Rose, F A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2853-15f85d58dff8ac5e257e778e8ea8f230909f224e306b22aca19a77d239e008a43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1973</creationdate><topic>Animals</topic><topic>Cellular Interactions and Control Processes</topic><topic>Chromatography, Gel</topic><topic>Chromatography, Ion Exchange</topic><topic>Hydrogen-Ion Concentration</topic><topic>Kinetics</topic><topic>Liver - enzymology</topic><topic>Methods</topic><topic>Molecular Weight</topic><topic>Nitrophenols</topic><topic>Rats</topic><topic>Sulfatases - analysis</topic><topic>Sulfatases - isolation & purification</topic><topic>Temperature</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Worwood, M</creatorcontrib><creatorcontrib>Dodgson, K S</creatorcontrib><creatorcontrib>Hook, G E</creatorcontrib><creatorcontrib>Rose, F A</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Biochemical journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Worwood, M</au><au>Dodgson, K S</au><au>Hook, G E</au><au>Rose, F A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Problems associated with the assay of arylsulphatases A and B of rat tissues</atitle><jtitle>Biochemical journal</jtitle><addtitle>Biochem J</addtitle><date>1973-05-01</date><risdate>1973</risdate><volume>134</volume><issue>1</issue><spage>183</spage><epage>190</epage><pages>183-190</pages><issn>0264-6021</issn><issn>0306-3283</issn><eissn>1470-8728</eissn><abstract>A method for the separation and purification of rat liver arylsulphatases A and B by gel filtration on Sephadex G-200 is described. The properties of the A enzyme and its molecular weight are similar to those of the corresponding ox liver enzyme. The B enzymes were found to be dissimilar. The method already developed for the assay of the corresponding enzymes from human tissues was shown to be unsuitable for the assay of the enzymes of rat tissues. A method of assay was developed which permits an approximate determination of the individual rat liver enzymes in a mixture of the two, but precise determination requires prior separation of the enzymes by gel-filtration chromatography.</abstract><cop>England</cop><pmid>4723220</pmid><doi>10.1042/bj1340183</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Cellular Interactions and Control Processes Chromatography, Gel Chromatography, Ion Exchange Hydrogen-Ion Concentration Kinetics Liver - enzymology Methods Molecular Weight Nitrophenols Rats Sulfatases - analysis Sulfatases - isolation & purification Temperature Time Factors |
title | Problems associated with the assay of arylsulphatases A and B of rat tissues |
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