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Related Concept Videos

Immunogold Electron Microscopy01:20

Immunogold Electron Microscopy

Immunoelectron microscopy utilizes immunogold labeling of endogenous proteins with specific antibodies to detect and localize these proteins in cells and tissues. The procedure provides insights into the distribution and quantification of protein under different stimulation conditions offering clues about their functions. Conjugating highly electron-dense gold particles with primary or secondary antibodies allow antigen detection on and within cells, with high resolution and specificity.
Enzyme-Linked Immunosorbent Assay01:33

Enzyme-Linked Immunosorbent Assay

In 1971, Peter Perlman and Eva Engvall developed an Enzyme-linked immunosorbent assay (ELISA or EIA). ELISA differs from western blot in that the assays are conducted in microtiter plates or in vivo rather than on an absorbent membrane.
There are many different types of ELISAs, but they all involve an antibody molecule whose constant region binds an enzyme, leaving the variable region free to bind its specific antigen.  Enzyme-substrate reaction allows the antigen to be visualized or quantified.

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Related Experiment Video

Updated: May 21, 2026

Fabricating a UV-Vis and Raman Spectroscopy Immunoassay Platform
09:02

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Published on: November 10, 2016

A SERS-based immunoassay with highly increased sensitivity using gold/silver core-shell nanorods.

Lei Wu1, Zhuyuan Wang, Shenfei Zong

  • 1Advanced Photonics Center, School of Electronic Science and Engineering, Southeast University, Nanjing 210096 Jiangsu, PR China.

Biosensors & Bioelectronics
|June 1, 2012
PubMed
Summary

Researchers developed a highly sensitive immunoassay using gold/silver core-shell nanorods for surface-enhanced Raman scattering (SERS). This novel SERS probe significantly improves detection limits for biological sensing applications.

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Last Updated: May 21, 2026

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Area of Science:

  • Nanotechnology
  • Biomedical Engineering
  • Analytical Chemistry

Background:

  • Surface-enhanced Raman scattering (SERS) offers high sensitivity for molecular detection.
  • Gold nanorods are commonly used in SERS-based assays but have limitations in sensitivity.
  • Developing more sensitive SERS probes is crucial for advancing biological sensing.

Purpose of the Study:

  • To develop a highly sensitive immunoassay using novel gold/silver core-shell nanorods.
  • To characterize the properties and SERS activity of these core-shell nanorods.
  • To evaluate the performance of the developed immunoassay in terms of detection limit and sensitivity.

Main Methods:

  • Fabrication and characterization of gold/silver core-shell nanorods using UV-vis spectroscopy, TEM, EDX, and SERS.
  • Modification of nanorods with antibodies for immunoassay development.
  • Quantification of antigen concentration using SERS spectra and dose-response curves.

Main Results:

  • Gold/silver core-shell nanorods exhibited significantly higher SERS activity compared to uncoated gold nanorods.
  • The immunoassay demonstrated antigen concentration-dependent SERS spectra.
  • A detection limit as low as 70 fM was achieved, representing a 10,000-fold improvement over gold nanorod-based detection.

Conclusions:

  • Gold/silver core-shell nanorods are superior SERS probes for immunoassays due to enhanced sensitivity.
  • These nanorods offer a significant advancement over traditional gold nanorods in SERS-based detection.
  • The developed SERS probes show great potential for various biological sensing applications.