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Ten Approaches That Improve Immunostaining: A Review of the Latest Advances for the Optimization of Immunofluorescence. | LitMetric

AI Article Synopsis

  • Immunostaining is a crucial technique for pinpointing protein locations in cells and tissues by using antibodies with various markers, mainly in immunofluorescence for research and diagnosis.
  • The technique has its challenges, such as fixing samples and managing antibody incubation times, which necessitate continual improvements in established protocols.
  • This review offers optimized methods for immunofluorescence and introduces a new antibody signal enhancer that boosts detection signals, particularly in cervical cancer and fibrous tissues, making it useful for both seasoned and novice researchers.

Article Abstract

Immunostaining has emerged as one of the most common and valuable techniques that allow the localization of proteins at a quantitative level within cells and tissues using antibodies coupled to enzymes, fluorochromes, or colloidal nanogold particles. The application of fluorochromes during immunolabeling is referred to as immunofluorescence, a method coupled to widefield or confocal microscopy and extensively applied in basic research and clinical diagnosis. Notwithstanding, there are still disadvantages associated with the application of this technique due to technical challenges in the process, such as sample fixation, permeabilization, antibody incubation times, and fluid exchange, etc. These disadvantages call for continuous updates and improvements to the protocols extensively described in the literature. This review contributes to protocol optimization, outlining 10 current methods for improving sample processing in different stages of immunofluorescence, including a section with further recommendations. Additionally, we have extended our own antibody signal enhancer method, which was reported to significantly increase antibody signals and is useful for cervical cancer detection, to improve the signals of fluorochrome-conjugated staining reagents in fibrous tissues. In summary, this review is a valuable tool for experienced researchers and beginners when planning or troubleshooting the immunofluorescence assay.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8836139PMC
http://dx.doi.org/10.3390/ijms23031426DOI Listing

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