Title : Purification of insulin-binding antibody by affinity chromatography using monocomponent insulin as ligand.

Pub. Date : 1985 Dec

PMID : 3915264






9 Functional Relationships(s)
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Protein Name
Organism
1 Adding native MC insulin to a competitive radioimmunoassay suppressed the IBA titer obtained with MC insulin more than that obtained with Cr insulin. Methylcholanthrene insulin Homo sapiens
2 Adding native MC insulin to a competitive radioimmunoassay suppressed the IBA titer obtained with MC insulin more than that obtained with Cr insulin. Methylcholanthrene insulin Homo sapiens
3 Adding native MC insulin to a competitive radioimmunoassay suppressed the IBA titer obtained with MC insulin more than that obtained with Cr insulin. Methylcholanthrene insulin Homo sapiens
4 Adding native MC insulin to a competitive radioimmunoassay suppressed the IBA titer obtained with MC insulin more than that obtained with Cr insulin. Methylcholanthrene insulin Homo sapiens
5 Adding native MC insulin to a competitive radioimmunoassay suppressed the IBA titer obtained with MC insulin more than that obtained with Cr insulin. Methylcholanthrene insulin Homo sapiens
6 Adding native MC insulin to a competitive radioimmunoassay suppressed the IBA titer obtained with MC insulin more than that obtained with Cr insulin. Methylcholanthrene insulin Homo sapiens
7 By adding native proinsulin in a similar assay system, the PBA titer obtained with Cr insulin was suppressed more than that extracted with MC insulin. Methylcholanthrene insulin Homo sapiens
8 By adding native proinsulin in a similar assay system, the PBA titer obtained with Cr insulin was suppressed more than that extracted with MC insulin. Methylcholanthrene insulin Homo sapiens
9 Using MC insulin, instead of Cr insulin, as the ligand in affinity chromatography increased the purity of recovered IBA. Methylcholanthrene insulin Homo sapiens