Protein unfolding allows use of commercial antibodies in an apolipoprotein M sandwich ELISA

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Standard

Protein unfolding allows use of commercial antibodies in an apolipoprotein M sandwich ELISA. / Bosteen, Markus Høybye; Dahlbäck, Björn; Nielsen, Lars Bo; Christoffersen, Christina.

I: Journal of Lipid Research, Bind 56, Nr. 3, 01.03.2015, s. 754-759.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Bosteen, MH, Dahlbäck, B, Nielsen, LB & Christoffersen, C 2015, 'Protein unfolding allows use of commercial antibodies in an apolipoprotein M sandwich ELISA', Journal of Lipid Research, bind 56, nr. 3, s. 754-759. https://doi.org/10.1194/jlr.D055947

APA

Bosteen, M. H., Dahlbäck, B., Nielsen, L. B., & Christoffersen, C. (2015). Protein unfolding allows use of commercial antibodies in an apolipoprotein M sandwich ELISA. Journal of Lipid Research, 56(3), 754-759. https://doi.org/10.1194/jlr.D055947

Vancouver

Bosteen MH, Dahlbäck B, Nielsen LB, Christoffersen C. Protein unfolding allows use of commercial antibodies in an apolipoprotein M sandwich ELISA. Journal of Lipid Research. 2015 mar. 1;56(3):754-759. https://doi.org/10.1194/jlr.D055947

Author

Bosteen, Markus Høybye ; Dahlbäck, Björn ; Nielsen, Lars Bo ; Christoffersen, Christina. / Protein unfolding allows use of commercial antibodies in an apolipoprotein M sandwich ELISA. I: Journal of Lipid Research. 2015 ; Bind 56, Nr. 3. s. 754-759.

Bibtex

@article{4ed8473d67eb4e8ea32e866ae565ac3c,
title = "Protein unfolding allows use of commercial antibodies in an apolipoprotein M sandwich ELISA",
abstract = "apoM is a member of the lipocalin superfamily and circulates in plasma attached to HDL particles. apoM plays a role in cholesterol metabolism and has recently been identified as transporter for the signaling lipid, sphingosine-1-phosphate (S1P), in plasma. S1P is implicated in several inflammatory diseases such as multiple sclerosis and rheumatoid arthritis. The ability to accurately measure apoM is crucial for investigating its biological functions and possible clinical implications. However, reliable commercial methods have been lacking so far. Therefore, we have developed an assay that specifically recognizes human apoM in plasma using commercially available reagents. Commercial apoM antibodies were screened for compatibility in a sandwich ELISA-based assay. One optimal pair of antibodies was chosen, and sample preparation, buffers, and incubation times were optimized to generate a simple and reproducible method. Validation and comparison to a previously described ELISA for apoM confirmed that the assay displays a high degree of sensitivity, specificity, and precision. Our results show that commercially available antibodies can be used to accurately measure human plasma apoM. This method can be implemented in every laboratory and will help promote high quality research.",
author = "Bosteen, {Markus H{\o}ybye} and Bj{\"o}rn Dahlb{\"a}ck and Nielsen, {Lars Bo} and Christina Christoffersen",
note = "Copyright {\textcopyright} 2015 by the American Society for Biochemistry and Molecular Biology, Inc.",
year = "2015",
month = mar,
day = "1",
doi = "10.1194/jlr.D055947",
language = "English",
volume = "56",
pages = "754--759",
journal = "Journal of Lipid Research",
issn = "0022-2275",
publisher = "American Society for Biochemistry and Molecular Biology, Inc.",
number = "3",

}

RIS

TY - JOUR

T1 - Protein unfolding allows use of commercial antibodies in an apolipoprotein M sandwich ELISA

AU - Bosteen, Markus Høybye

AU - Dahlbäck, Björn

AU - Nielsen, Lars Bo

AU - Christoffersen, Christina

N1 - Copyright © 2015 by the American Society for Biochemistry and Molecular Biology, Inc.

PY - 2015/3/1

Y1 - 2015/3/1

N2 - apoM is a member of the lipocalin superfamily and circulates in plasma attached to HDL particles. apoM plays a role in cholesterol metabolism and has recently been identified as transporter for the signaling lipid, sphingosine-1-phosphate (S1P), in plasma. S1P is implicated in several inflammatory diseases such as multiple sclerosis and rheumatoid arthritis. The ability to accurately measure apoM is crucial for investigating its biological functions and possible clinical implications. However, reliable commercial methods have been lacking so far. Therefore, we have developed an assay that specifically recognizes human apoM in plasma using commercially available reagents. Commercial apoM antibodies were screened for compatibility in a sandwich ELISA-based assay. One optimal pair of antibodies was chosen, and sample preparation, buffers, and incubation times were optimized to generate a simple and reproducible method. Validation and comparison to a previously described ELISA for apoM confirmed that the assay displays a high degree of sensitivity, specificity, and precision. Our results show that commercially available antibodies can be used to accurately measure human plasma apoM. This method can be implemented in every laboratory and will help promote high quality research.

AB - apoM is a member of the lipocalin superfamily and circulates in plasma attached to HDL particles. apoM plays a role in cholesterol metabolism and has recently been identified as transporter for the signaling lipid, sphingosine-1-phosphate (S1P), in plasma. S1P is implicated in several inflammatory diseases such as multiple sclerosis and rheumatoid arthritis. The ability to accurately measure apoM is crucial for investigating its biological functions and possible clinical implications. However, reliable commercial methods have been lacking so far. Therefore, we have developed an assay that specifically recognizes human apoM in plasma using commercially available reagents. Commercial apoM antibodies were screened for compatibility in a sandwich ELISA-based assay. One optimal pair of antibodies was chosen, and sample preparation, buffers, and incubation times were optimized to generate a simple and reproducible method. Validation and comparison to a previously described ELISA for apoM confirmed that the assay displays a high degree of sensitivity, specificity, and precision. Our results show that commercially available antibodies can be used to accurately measure human plasma apoM. This method can be implemented in every laboratory and will help promote high quality research.

U2 - 10.1194/jlr.D055947

DO - 10.1194/jlr.D055947

M3 - Journal article

C2 - 25561460

VL - 56

SP - 754

EP - 759

JO - Journal of Lipid Research

JF - Journal of Lipid Research

SN - 0022-2275

IS - 3

ER -

ID: 137357504