1978
DOI: 10.1111/j.1365-3083.1978.tb00492.x
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Protein A Reactivity of Various Mammalian Immunoglobulins

Abstract: Serum samples and immunoglobulin fractions of eight mammalian species were applied to a Sepharose--protein A column. As with the human immunoglobulin subclasses IgG1, IgG2 and IgG4, all examined IgG classes and subclasses were bound to a greater or lesser extent to protein A. However, the binding of IgG1 of ruminants was very poor. Polyclonal IgM and IgA of the pig, the dog and the cat may be separated in protein A reactive and protein A non-reactive fractions. In addition, monoclonal canine IgM and IgA partia… Show more

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Cited by 286 publications
(76 citation statements)
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“…Binding of antibodies to the protein A moiety was first demonstrated on purified particles by using immunogold labeling. Because protein A binds efficiently to the constant regions of many subclasses of IgG from different species (19), this test could be done either directly by using any gold-conjugated antibody or indirectly by using a primary unlabeled and a secondary gold-conjugated antibody. Although the first approach already gave good results (data not shown), these were further improved by including a secondary antibody.…”
Section: Cp-protein a Fusion Is Expressed At A High Level In Plant Timentioning
confidence: 99%
“…Binding of antibodies to the protein A moiety was first demonstrated on purified particles by using immunogold labeling. Because protein A binds efficiently to the constant regions of many subclasses of IgG from different species (19), this test could be done either directly by using any gold-conjugated antibody or indirectly by using a primary unlabeled and a secondary gold-conjugated antibody. Although the first approach already gave good results (data not shown), these were further improved by including a secondary antibody.…”
Section: Cp-protein a Fusion Is Expressed At A High Level In Plant Timentioning
confidence: 99%
“…Rabbit antibody against G6PD was prepared as described by DeFlora et al (1977). Anti-G6PD IgG was purified from rabbit serum by (NH&SO, precipitation, DE-52 cellulose column chromatography (Weir, 1967), and affinity chromatography on a protein A-Sepharose CL-4B column (Goudswaard et al, 1978). Heparin (20 u/ml) was added to the antibody preparation to inhibit RNase activity.…”
Section: (A) Purification Of Glucosed-phosphate Dehydrogenase and Prementioning
confidence: 99%
“…Rabbit antisera could be used after simple affinity chromatography with protein A (Goudswaard et al, 1978 …”
Section: Cerebrospinal Fluidmentioning
confidence: 99%