APA Style
Karina, C. , Karina, C. B, M. S. , B, M. S. Gladys, R. V. , Gladys, R. V. Guillermo, D. , & Guillermo, D. (2022). Development of a Competitive Enzyme Immunoassay Technique for the Detection of Peanut Traces in Gluten-free Products.
Universal Journal of Physics Research, 1(1), 46-55.
https://doi.org/10.31586/ujfst.2022.540
ACS Style
Karina, C. ; Karina, C. B, M. S. ; B, M. S. Gladys, R. V. ; Gladys, R. V. Guillermo, D. ; Guillermo, D. Development of a Competitive Enzyme Immunoassay Technique for the Detection of Peanut Traces in Gluten-free Products.
Universal Journal of Physics Research 2022 1(1), 46-55.
https://doi.org/10.31586/ujfst.2022.540
Chicago/Turabian Style
Karina, Cellerino, Cellerino Karina. Márquez Silvina B, Márquez Silvina B. Rodríguez Viviana Gladys, Rodríguez Viviana Gladys. Docena Guillermo, and Docena Guillermo. 2022. "Development of a Competitive Enzyme Immunoassay Technique for the Detection of Peanut Traces in Gluten-free Products".
Universal Journal of Physics Research 1, no. 1: 46-55.
https://doi.org/10.31586/ujfst.2022.540
AMA Style
Karina C, Karina CB MS, B MSGladys RV, Gladys RVGuillermo D, Guillermo D. Development of a Competitive Enzyme Immunoassay Technique for the Detection of Peanut Traces in Gluten-free Products.
Universal Journal of Physics Research. 2022; 1(1):46-55.
https://doi.org/10.31586/ujfst.2022.540
@Article{ujpr540,
AUTHOR = {Karina, Cellerino and B, Márquez Silvina and Gladys, Rodríguez Viviana and Guillermo, Docena and Beatriz, López Laura},
TITLE = {Development of a Competitive Enzyme Immunoassay Technique for the Detection of Peanut Traces in Gluten-free Products},
JOURNAL = {Universal Journal of Physics Research},
VOLUME = {1},
YEAR = {2022},
NUMBER = {1},
PAGES = {46-55},
URL = {https://www.scipublications.com/journal/index.php/UJFST/article/view/540},
ISSN = {2834-5479},
DOI = {10.31586/ujfst.2022.540},
ABSTRACT = {The aim of this work was to develop a competititve enzymeimmunoassay technique, to detect the presence of traces of peanut in gluten-free products. Specific rabbit polyclonal antiserum against peanut was used as primary antibody. The optimal antigen concentration to be immobilized on the plate and the concentration of primary antibody to be used in competition was determined. The calibration curve was fitted using increasing concentrations of an extract of peanut product. The peanut product was extracted with Tris-HCl buffer 0.0625M with 3% sodium dodecylsulfate (SDS) and 2% sulphite (S) 0,1 M. All validation parameters studied were appropriate. Commercial samples of gluten-free products were analysed with this enzyme immunoassays and a commercial ELISA kit. Significant differences were observed in the quantitative results obtained with both methods; nevertheless the developed enzyme immunoassay could be used as screening method.},
}
%0 Journal Article
%A Karina, Cellerino
%A B, Márquez Silvina
%A Gladys, Rodríguez Viviana
%A Guillermo, Docena
%A Beatriz, López Laura
%D 2022
%J Universal Journal of Physics Research
%@ 2834-5479
%V 1
%N 1
%P 46-55
%T Development of a Competitive Enzyme Immunoassay Technique for the Detection of Peanut Traces in Gluten-free Products
%M doi:10.31586/ujfst.2022.540
%U https://www.scipublications.com/journal/index.php/UJFST/article/view/540
TY - JOUR
AU - Karina, Cellerino
AU - B, Márquez Silvina
AU - Gladys, Rodríguez Viviana
AU - Guillermo, Docena
AU - Beatriz, López Laura
TI - Development of a Competitive Enzyme Immunoassay Technique for the Detection of Peanut Traces in Gluten-free Products
T2 - Universal Journal of Physics Research
PY - 2022
VL - 1
IS - 1
SN - 2834-5479
SP - 46
EP - 55
UR - https://www.scipublications.com/journal/index.php/UJFST/article/view/540
AB - The aim of this work was to develop a competititve enzymeimmunoassay technique, to detect the presence of traces of peanut in gluten-free products. Specific rabbit polyclonal antiserum against peanut was used as primary antibody. The optimal antigen concentration to be immobilized on the plate and the concentration of primary antibody to be used in competition was determined. The calibration curve was fitted using increasing concentrations of an extract of peanut product. The peanut product was extracted with Tris-HCl buffer 0.0625M with 3% sodium dodecylsulfate (SDS) and 2% sulphite (S) 0,1 M. All validation parameters studied were appropriate. Commercial samples of gluten-free products were analysed with this enzyme immunoassays and a commercial ELISA kit. Significant differences were observed in the quantitative results obtained with both methods; nevertheless the developed enzyme immunoassay could be used as screening method.
DO - Development of a Competitive Enzyme Immunoassay Technique for the Detection of Peanut Traces in Gluten-free Products
TI - 10.31586/ujfst.2022.540
ER -