Determination of glutamic acid decarboxylase antibodies (GADA) IgG subclasses - comparison of three immunoprecipitation assays (IPAs)
(2007) In Clinical and Experimental Immunology 150(1). p.68-74- Abstract
- IgG subclasses of glutamic acid decarboxylase (GAD(65)) antibodies (GADA) may reflect the immunological state in the pancreas of GADA-positive patients with autoimmune diabetes. The use of biotin-conjugated antibodies and streptavidin Sepharose are used commonly in immunoprecipitation assays (IPA) based on (125)I- or (35)S-labelled antigens to capture IgG subclasses directed against IA-2 or GAD(65). We have compared three different immunoprecipitation assays for the determination of GADA IgG subclasses. Two of the assays were based on the biotin and streptavidin systems provided in a solid (immobilized) or liquid (mobilized) phase binding environment. The third assay was based on N-hydroxysuccinimide (immobilized) interaction with primary... (More)
- IgG subclasses of glutamic acid decarboxylase (GAD(65)) antibodies (GADA) may reflect the immunological state in the pancreas of GADA-positive patients with autoimmune diabetes. The use of biotin-conjugated antibodies and streptavidin Sepharose are used commonly in immunoprecipitation assays (IPA) based on (125)I- or (35)S-labelled antigens to capture IgG subclasses directed against IA-2 or GAD(65). We have compared three different immunoprecipitation assays for the determination of GADA IgG subclasses. Two of the assays were based on the biotin and streptavidin systems provided in a solid (immobilized) or liquid (mobilized) phase binding environment. The third assay was based on N-hydroxysuccinimide (immobilized) interaction with primary amines (i.e. lysine residues) on the antibody. We found the liquid phase binding assay (LPBA) to be the most stable assay, with a comparatively low coefficient of variation and background. (Less)
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/1142365
- author
- Hillman, Magnus LU ; Törn, Carina LU and Landin-Olsson, Mona LU
- organization
- publishing date
- 2007
- type
- Contribution to journal
- publication status
- published
- subject
- in
- Clinical and Experimental Immunology
- volume
- 150
- issue
- 1
- pages
- 68 - 74
- publisher
- British Society for Immunology
- external identifiers
-
- pmid:17666094
- wos:000249275500008
- scopus:34548526770
- ISSN
- 0009-9104
- DOI
- 10.1111/j.1365-2249.2007.03473.x
- language
- English
- LU publication?
- yes
- id
- 374a8f53-189e-47cc-916f-bec737f3c9fb (old id 1142365)
- date added to LUP
- 2016-04-01 11:47:32
- date last changed
- 2024-01-07 20:38:19
@article{374a8f53-189e-47cc-916f-bec737f3c9fb, abstract = {{IgG subclasses of glutamic acid decarboxylase (GAD(65)) antibodies (GADA) may reflect the immunological state in the pancreas of GADA-positive patients with autoimmune diabetes. The use of biotin-conjugated antibodies and streptavidin Sepharose are used commonly in immunoprecipitation assays (IPA) based on (125)I- or (35)S-labelled antigens to capture IgG subclasses directed against IA-2 or GAD(65). We have compared three different immunoprecipitation assays for the determination of GADA IgG subclasses. Two of the assays were based on the biotin and streptavidin systems provided in a solid (immobilized) or liquid (mobilized) phase binding environment. The third assay was based on N-hydroxysuccinimide (immobilized) interaction with primary amines (i.e. lysine residues) on the antibody. We found the liquid phase binding assay (LPBA) to be the most stable assay, with a comparatively low coefficient of variation and background.}}, author = {{Hillman, Magnus and Törn, Carina and Landin-Olsson, Mona}}, issn = {{0009-9104}}, language = {{eng}}, number = {{1}}, pages = {{68--74}}, publisher = {{British Society for Immunology}}, series = {{Clinical and Experimental Immunology}}, title = {{Determination of glutamic acid decarboxylase antibodies (GADA) IgG subclasses - comparison of three immunoprecipitation assays (IPAs)}}, url = {{http://dx.doi.org/10.1111/j.1365-2249.2007.03473.x}}, doi = {{10.1111/j.1365-2249.2007.03473.x}}, volume = {{150}}, year = {{2007}}, }