SIMPLE: a sequential immunoperoxidase labeling and erasing method

J Histochem Cytochem. 2009 Oct;57(10):899-905. doi: 10.1369/jhc.2009.953612. Epub 2009 Apr 13.

Abstract

The ability to simultaneously visualize expression of multiple antigens in cells and tissues can provide powerful insights into cellular and organismal biology. However, standard methods are limited to the use of just two or three simultaneous probes and have not been widely adopted for routine use in paraffin-embedded tissue. We have developed a novel approach called sequential immunoperoxidase labeling and erasing (SIMPLE) that enables the simultaneous visualization of at least five markers within a single tissue section. Utilizing the alcohol-soluble peroxidase substrate 3-amino-9-ethylcarbazole, combined with a rapid non-destructive method for antibody-antigen dissociation, we demonstrate the ability to erase the results of a single immunohistochemical stain while preserving tissue antigenicity for repeated rounds of labeling. SIMPLE is greatly facilitated by the use of a whole-slide scanner, which can capture the results of each sequential stain without any information loss.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Animals
  • Antibodies
  • Biomarkers / metabolism
  • Brain / metabolism
  • Calbindins
  • Carbazoles*
  • Coloring Agents
  • Glial Fibrillary Acidic Protein
  • Humans
  • Immunoenzyme Techniques / methods*
  • Mice
  • Microtubule-Associated Proteins / immunology
  • Microtubule-Associated Proteins / metabolism
  • Nerve Growth Factors / immunology
  • Nerve Growth Factors / metabolism
  • Nerve Tissue Proteins / immunology
  • Nerve Tissue Proteins / metabolism
  • Neurofilament Proteins / immunology
  • Neurofilament Proteins / metabolism
  • Pituitary Gland / metabolism
  • S100 Calcium Binding Protein G / immunology
  • S100 Calcium Binding Protein G / metabolism
  • S100 Calcium Binding Protein beta Subunit
  • S100 Proteins / immunology
  • S100 Proteins / metabolism
  • Staining and Labeling / methods

Substances

  • Antibodies
  • Biomarkers
  • Calbindins
  • Carbazoles
  • Coloring Agents
  • Glial Fibrillary Acidic Protein
  • Microtubule-Associated Proteins
  • Mtap2 protein, mouse
  • Nerve Growth Factors
  • Nerve Tissue Proteins
  • Neurofilament Proteins
  • S100 Calcium Binding Protein G
  • S100 Calcium Binding Protein beta Subunit
  • S100 Proteins
  • glial fibrillary astrocytic protein, mouse
  • neurofilament protein M
  • 3-amino-9-ethylcarbazole