Long-term preservation of antigenicity on tissue microarrays View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

2004-08

AUTHORS

Kyle A DiVito, Lori A Charette, David L Rimm, Robert L Camp

ABSTRACT

Tissue microarrays have facilitated the evaluation of large cohort studies; however, there is little data on the best method for preserving sections once they are cut. We assessed three methods of storing precut breast cancer microarray slides: paraffin coating and storage in a nitrogen desiccator, either alone or in combination. We tested the durability of three antigens, cytokeratin, estrogen receptor, and Ki-67 on microarrays stored under these conditions for 3 months at room temperature. Staining was assessed with both manual scoring using traditional brown stain (0-3+) as well as automated scoring using fluorescently stained sections. Staining intensity was compared to that obtained from freshly cut slides. Slides stored under ambient conditions (room temperature and air) for 3 months exhibited marked degradation of all target antigens, in some cases resulting in slides that were virtually unreadable. We found that combined paraffin coating and nitrogen storage resulted in the best preservation of antigenicity, with retention of 72-99% of the antigenicity of a freshly cut slide, depending upon the marker and detection system used. The use of either paraffin coating or nitrogen storage alone protected slides to a lesser degree. More... »

PAGES

3700131

Identifiers

URI

http://scigraph.springernature.com/pub.10.1038/labinvest.3700131

DOI

http://dx.doi.org/10.1038/labinvest.3700131

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1016844806

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/15195116


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