“…[1][2][3][4][5] However, in at ypicalE LISA,a tl east one round of additional enzyme-catalyzed signalt ransducing step is essential after the immunoreaction, which makes the operation rather complicated.M oreover,the activities of enzymes in ELISAs, such as the commonly used alkaline phosphatase( ALP) and horseradish peroxidase (HRP),a re prone to be affected by the environmental factors and reactionm edia, which may lead to poor assay reproducibility.M ore importantly,b ecause of its compromising sensitivity,t raditional ELISA usually cannotd etect antigens within the limits of criticalt hreshold concentrations till the patient has already suffered as erious situation. [8] To tackle this issue, some new signala mplification approaches based on nanomaterial labels or DNA amplification techniques have been introduced to complementt he traditional ELISAs in order to enhancet he detection sensitivity with higher stability. [9][10][11][12][13][14][15][16][17][18][19][20][21] Although quite sensitivef or antigen detection, these adapted ELISAss uffer heavily from the drawbacks such as cumbersome multi-step operations, delicate antibody modification/bioconjugation, and expensive reagents.…”