Development of ic-ELISA for Furosine Detection Based on Polyclonal Antibodies
CSTR:
Author:
Affiliation:

Clc Number:

TS 207

Fund Project:

  • Article
  • |
  • Figures
  • |
  • Metrics
  • |
  • Reference
  • |
  • Related
  • |
  • Cited by
  • |
  • Materials
  • |
  • Comments
    Abstract:

    A complete furosine complete antigen was prepared using the formaldehyde method, and cross-verification was employed to ensure the specificity of the polyclonal antibodies. An indirect competitive enzyme-linked immunosorbent assay(ic-ELISA) was successfully established based on the antibodies. The results demonstrated that the established ic-ELISA exhibited a detection range of 12.20 to 2 143.42 ng/mL, with a limit of detection (LOD) at 2.69 ng/mL. This method is simple, rapid, and cost-effective, offering high sensitivity and excellent specificity. It provides a novel option for the efficient detection of furosine in food, demonstrating its potential for practical application.

    Reference
    Related
    Cited by
Get Citation

YANG Min-yi, LUO Wen-qian, JIA Rong-ye, LIU Yu-xuan, WANG Rong-zhi. Development of ic-ELISA for Furosine Detection Based on Polyclonal Antibodies[J]. Journal of Food Science and Biotechnology,2024,43(5):138-145.

Copy
Related Videos

Article Metrics
  • Abstract:
  • PDF:
  • HTML:
  • Cited by:
History
  • Received:
  • Revised:
  • Adopted:
  • Online: July 18,2024
  • Published:
Article QR Code

Copy Right:Editorial Board of Journal of Food Science and Biotechnology

Address:No. 1800, Lihu Avenue, Wuxi 214122, Jiangsu Province,China  PostCode:214122

Phone:0510-85913526  E-mail:xbbjb@jiangnan.edu.cn

Supported by:Beijing E-Tiller Technology Development Co., Ltd.

WeChat

Mobile website