Development and application of monoclonal antibodies anti-human lipoprotein-associated phospholipase A2 / 生物工程学报
Chinese Journal of Biotechnology
; (12): 482-491, 2019.
Article
Dans Zh
| WPRIM
| ID: wpr-771359
Responsable en Bibliothèque :
WPRO
ABSTRACT
The aim of this study is to prepare monoclonal anti-human Lp-PLA2 antibodies, and establish a rapid and accurate immunochromatographic Lp-PLA2 assay used in community medical institution. The gene sequence of human Lp-PLA2 was obtained from NCBI to construct the expression plasmid. Lp-PLA2 protein expressed in CHO-K1 cells was used to immune BALB/c mice. The monoclonal antibodies were produced in mouse ascites after hybridoma cells screening. Antibodies were evaluated by SDS-PAGE, ELISA and other methods. The Lp-PLA2 test strip was prepared based on sandwich method and evaluated with the portable detection instrument. The affinity of the paired antibodies, PLA1 and PLA5, both reached 1×10⁻⁸. The antibody subclass was IgG1. Both antibodies recognized the Lp-PLA2 protein in the blood specifically. The Lp-PLA2 test strip was prepared based on sandwich method, with linear range of 20-2000 ng/mL. The Lp-PLA2 test strip correlated well with the diaDexus ELISA test kit. In conclusion, the paired antibodies were successfully prepared with high affinity and specificity. The immunochromatographic test of Lp-PLA2 provided a fast and accurate method to detect the concentration of Lp-PLA2 in blood sample for clinical use in the community medical institution and could contribute to the management of cardiovascular diseases.
Texte intégral:
1
Indice:
WPRIM
Sujet Principal:
Test ELISA
/
1-Alkyl-2-acetylglycerophosphocholine esterase
/
Métabolisme
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Souris de lignée BALB C
/
Anticorps monoclonaux
Limites du sujet:
Animals
/
Humans
langue:
Zh
Texte intégral:
Chinese Journal of Biotechnology
Année:
2019
Type:
Article