Publication: An optimized xylene-free protein extraction method adapted to formalin-fixed paraffin embedded tissue sections for western blot analysis
Authors
Mansour, Anthony G. ; Abou Khalil, Pamela ; Bejjani, Noha ; Chatila, Rajaa ; Dagher Hamalian, Carole ; Faour, Wissam H.
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Publisher
Universidad de Murcia. Departamento de Biología Celular e Histología
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DOI
DOI: 10.14670/HH-11-789
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info:eu-repo/semantics/article
Description
Abstract
Deparaffinization of formalin-fixed paraffin
embedded (FFPE) tissues with xylene currently remains
a major challenge to the biomedical community. We
developed an efficient xylene-free protocol to isolate
proteins from archived FFPE human tissue sections. A
total of 79 different types of FFPE tissue sections of 8
µm thickness were obtained from various archived FFPE
specimens. Deparaffinization was conducted by gently
washing each section with around 1 ml of hot distilled
water (≈80°C). The deparaffinized tissues were
homogenized in lysis buffer, and the isolated proteins
were quantified and efficiently resolved using western
blot analysis for the presence of Protein kinase B
(PKB/AKT) and β-actin. Moreover, a significant amount
of proteins was successfully isolated with an average of
2.31 µg/µl. The migration pattern of AKT and β-actin
obtained from the specimens was similar to the positive
control obtained from protein lysates prepared from in
vitro cultured MDA231 cancer cell lines. AKT was
successfully identified in all specimens, and β-actin
protein was resolved with an efficiency higher than 80%.
The entire extraction procedure requires only 20
minutes. This newly developed technique is an efficient,
safe, cost-effective, and rapid method to isolate proteins
from FFPE tissue sections adequate for molecular
analysis.
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Citation
Histology and Histopathology, Vol.32, nº3, (2017)
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Este ítem está sujeto a una licencia Creative Commons. http://creativecommons.org/licenses/by-nc-nd/4.0/