Yun Hanool, Jeong Hee-Jin
Department of Biological and Chemical Engineering, Hongik University, 2639 Sejong-ro, Sejong-si 30016, South Korea.
Department of Biological and Chemical Engineering, Hongik University, 2639 Sejong-ro, Sejong-si 30016, South Korea.
Spectrochim Acta A Mol Biomol Spectrosc. 2024 Apr 5;310:123973. doi: 10.1016/j.saa.2024.123973. Epub 2024 Jan 29.
The development of accurate and high-throughput biomarker detection tools is crucial for the diagnosis, monitoring, and treatment of various diseases. In this study, a sensitive fluorogenic enzyme-linked immunosorbent assay (FELISA) using Amplex Red or QuantaBlu fluorescent substrate was developed for the detection of tumor necrosis factor alpha and programmed cell death-ligand 1. The limit of detection of FELISA was in the nanogram order and multiple samples were conveniently assayed within 20 h using FELISA, demonstrating its applicability as a powerful immunoassay tool. FELISA can be widely used for rapid and accurate TNFα and PDL1 detection and applied to various fluorogenic immunoassays against other antigens of interest.
开发准确且高通量的生物标志物检测工具对于各种疾病的诊断、监测和治疗至关重要。在本研究中,开发了一种使用Amplex Red或QuantaBlu荧光底物的灵敏荧光酶联免疫吸附测定法(FELISA),用于检测肿瘤坏死因子α和程序性细胞死亡配体1。FELISA的检测限在纳克级别,使用FELISA可在20小时内方便地对多个样品进行检测,证明了其作为强大免疫测定工具的适用性。FELISA可广泛用于快速准确地检测TNFα和PDL1,并应用于针对其他感兴趣抗原的各种荧光免疫测定。