Construction of prokaryotic expression vector of pig AANAT protein, method for preparing fusion protein and application thereof

By constructing a prokaryotic expression vector for porcine AANAT and preparing antibodies, the problem of detecting porcine AANAT protein was solved, achieving efficient and specific detection of porcine AANAT protein and meeting the needs of immunological and functional research.

CN122405618APending Publication Date: 2026-07-17YANGZHOU UNIV
View PDF 0 Cites 0 Cited by

Patent Information

Application Number
CN202610573478.6
Authority / Receiving Office
CN · China
Patent Type
Applications(China)
Current Assignee / Owner
Filing Date
2026-04-28
Publication Date
2026-07-17

AI Technical Summary

Technical Problem

Existing technologies lack effective methods for detecting porcine AANAT proteins. Artificial synthesis is costly and has poor stability, while proteins prepared by peptide methods have insufficient immunogenicity, failing to meet the needs of immunological detection and functional research.

Method used

Amplification primers were designed and synthesized to construct the porcine AANAT prokaryotic expression vector pET32a(+)-pAANAT. The His-tag-pAANAT fusion protein was expressed using the BL21(DE3) recombinant protein expression strain. Soluble protein was obtained through purification, and polyclonal and monoclonal antibodies were prepared for the detection of porcine AANAT protein.

Benefits of technology

A His-tag-pAANAT fusion protein with high expression level and high purity was obtained. The prepared antibody can specifically bind to AANAT protein in porcine pineal gland tissue, providing efficient ELISA detection conditions.

✦ Generated by Eureka AI based on patent content.

Smart Images

  • Figure CN122405618A_ABST
    Figure CN122405618A_ABST
Patent Text Reader

Abstract

本发明公开了一种猪AANAT蛋白原核表达载体的构建、融合蛋白的制备方法及其应用,IPTG诱导BL21(DE3)‑pET32a(+)‑pAANAT重组蛋白表达菌株能够获得His‑tag‑pAANAT融合蛋白(抗原),并提供了利用该抗原制备猪AANAT多克隆抗体和猪AANAT单克隆抗体的方法及应用,本发明构建的猪AANAT融合蛋白表达载体和制备的His‑tag‑pAANAT融合蛋白,具有操作方法简单、成本低和可控性强的特点,通过本发明制备的猪AANAT多克隆抗体和猪AANAT单克隆抗体特异性强、成本低廉,能够用于检测猪AANAT蛋白。
Need to check novelty before this filing date? Find Prior Art