2015
DOI: 10.1016/j.jchromb.2015.06.003
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Development of an aptamer-affinity chromatography for efficient single step purification of Concanavalin A from Canavalia ensiformis

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Cited by 22 publications
(10 citation statements)
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“…Due to its ability to enrich selective targets, affinity chromatography has remained a mainstay technique in separation chemistry [69][70][71][72] . In this study, both hCA I and II isoenzymes were purified by Sepharose-4B-L-tyrosine-sulfanilamide affinity chromatography [73][74][75][76] .…”
Section: Methodsmentioning
confidence: 99%
“…Due to its ability to enrich selective targets, affinity chromatography has remained a mainstay technique in separation chemistry [69][70][71][72] . In this study, both hCA I and II isoenzymes were purified by Sepharose-4B-L-tyrosine-sulfanilamide affinity chromatography [73][74][75][76] .…”
Section: Methodsmentioning
confidence: 99%
“…Aptamers have been used as 'antibody mimics' or alternatives to antibodies in some chromatographic binding assays [17][18][19][20]. These binding agents consist of single-stranded DNA or RNA sequences that are often 10 to 100 nucleotides in length and that have the ability to form highly ordered 3D structures [19].…”
Section: Antibodies and Related Binding Agentsmentioning
confidence: 99%
“…Aptamers are prepared through a selection and amplification process known as SELEX (i.e., the 'systematic evolution of ligands by exponential enrichment'), which can be used to generate specific binding agents with relatively high affinities for a particular target [17,18]. These agents have been used to bind targets that have included drugs, peptides, proteins and cells [17][18][19][20]. It is possible to easily modify the structure of an aptamer to include a label or to immobilize the aptamer to a support [18,19].…”
Section: Antibodies and Related Binding Agentsmentioning
confidence: 99%
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