AI Article Synopsis

  • Immunofluorescent staining is the preferred method for assessing protein levels in cell cultures where visual structure is important, but immunocytochemical staining on paraffin-embedded cells offers a viable alternative.
  • The immunocytochemical protocol used HeLa cells from paraffin cell blocks to evaluate proliferation markers CKAP2 and Ki-67, successfully preserving cell morphology.
  • Results showed that staining patterns for CKAP2 and Ki-67 in cell blocks were comparable to those obtained in paraffin cancer tissues, demonstrating that this method can effectively maintain structural integrity while allowing for protein expression analysis.

Article Abstract

Immunofluorescent staining is currently the method of choice for determination of protein expression levels in cell-culture systems when morphological information is also necessary. The protocol of immunocytochemical staining on paraffin-embedded cell blocks, presented herein, is an excellent alternative to immunofluorescent staining on non-paraffin-embedded fixed cells. In this protocol, a paraffin cell block from HeLa cells was prepared using the thromboplastin-plasma method, and immunocytochemistry was performed for the evaluation of two proliferation markers, CKAP2 and Ki-67. The nuclei and cytoplasmic morphology of the HeLa cells were well preserved in the cell-block slides. At the same time, the CKAP2 and Ki-67 staining patterns in the immunocytochemistry were quite similar to those in immunohistochemical staining in paraffin cancer tissues. With modified cell-culture conditions, including pre-incubation of HeLa cells under serum-free conditions, the effect could be evaluated while preserving architectural information. In conclusion, immunocytochemistry on paraffin-embedded cell blocks is an excellent alternative to immunofluorescent staining.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6101295PMC
http://dx.doi.org/10.3791/57369DOI Listing

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