| Literature DB >> 869934 |
Abstract
Human erythrocyte glycophorin was purified rapidly by (a) chromatography of a Triton X-100 extract of erythrocyte 'ghosts' on N-(3-carboxypropionyl)aminodecyl-Sepharose in buffers containing Triton X-100 or sodium dodecyl sulphate, or (b) chromatography of whole 'ghosts', solubilized in sodium dodecyl sulphate, on dodecyl-Sepharose, in buffers containing sodium dodecyl sulphate. The products contained 85-95% glycophorin (electrophoretic band PAS-1) and the major contaminants were glycoproteins PAS-2 (possibly a subunit of glycophorin) and PAS-3.Entities:
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Year: 1977 PMID: 869934 PMCID: PMC1164711 DOI: 10.1042/bj1630397
Source DB: PubMed Journal: Biochem J ISSN: 0264-6021 Impact factor: 3.857