scholarly journals Antibodies validated for routinely processed tissues stain frozen sections unpredictably

BioTechniques ◽  
2021 ◽  
Vol 70 (3) ◽  
pp. 137-148
Author(s):  
Maddalena M Bolognesi ◽  
Francesco Mascadri ◽  
Laura Furia ◽  
Mario Faretta ◽  
Francesca M Bosisio ◽  
...  

Background: Antibody validation for tissue staining is required for reproducibility; criteria to ensure validity have been published recently. The majority of these recommendations imply the use of routinely processed (formalin-fixed, paraffin-embedded) tissue. Materials & methods: We applied to lightly fixed frozen sections a panel of 126 antibodies validated for formalin-fixed, paraffin-embedded tissue with extended criteria. Results: Less than 30% of the antibodies performed as expected with all fixations. 35% preferred one fixation over another, 13% gave nonspecific staining and 23% did not stain at all. Conclusion: Individual antibody variability of the paratope’s fitness for the fixed antigen may be the cause. Revalidation of established antibody panels is required when they are applied to sections whose fixation and processing are different from the tissue where they were initially validated.


2012 ◽  
Vol 60 (6B) ◽  
pp. E37-E50 ◽  
Author(s):  
Claudia Schuster ◽  
Katharina Malinowsky ◽  
Sibylle Liebmann ◽  
Daniela Berg ◽  
Claudia Wolff ◽  
...  


2016 ◽  
Vol 6 (1) ◽  
Author(s):  
Camilla Natasha Cederbye ◽  
Jesper Andreas Palshof ◽  
Tine Plato Hansen ◽  
Anne Katrine Duun-Henriksen ◽  
Dorte Linnemann ◽  
...  


1997 ◽  
Vol 45 (5) ◽  
pp. 737-741 ◽  
Author(s):  
Helen Liapis ◽  
Karen Hutton

Integrins are heterodimeric transmembrane receptors, which are expressed in many cells. In vitro experiments have demonstrated that integrins may be important in tumor progression and organ development. The functions of integrins were previously studied in cell cultures and their tissue expression was detected by immunofluorescence or immunoperoxidase in frozen sections. The purpose of this study was to determine the optimal conditions for detection of integrins in formalin-fixed, paraffin-embedded tissues. We utilized microwave heating and enzyme digestion in routinely processed, surgically removed tissues. Our results demonstrate that integrins can be reliably detected in archival material. This approach will facilitate further investigation of the role played by integrins in human malignancies and in developmental processes.



2020 ◽  
Vol 30 (1) ◽  
pp. 8
Author(s):  
NasarYousuf Alwahaibi ◽  
RajaaMohammed Alsidiri ◽  
ThuraiyaAmer Alsinawi ◽  
WafaHamed Almalki ◽  
ShadiaSaid Alsinawi ◽  
...  


2020 ◽  
Author(s):  
Maddalena M Bolognesi ◽  
Francesco Mascadri ◽  
Roberto Perego ◽  
Silvia Bombelli ◽  
Francesca M Bosisio ◽  
...  

ABSTRACTA customized context-dependent validation of antibodies for the prospective use, rather than a general stamp of validity, is required for reproducibility and data validity, besides the need of standardized reagents. In-situ antibody staining is a technique broadly used in experimental settings and human diagnostic practice. The first typically, but not exclusively uses lightly fixed material (cell smears, frozen sections), the second, routinely processed formalin-fixed, paraffin-embedded (FFPE) tissue. Differently from techniques based on tissue extraction, there is little awareness of the context-dependent constraints inherent with either type of in situ staining except that antigen masking associated with routine tissue processing limits the range of useful antibodies. We applied a panel of 126 antibodies validated for FFPE to lightly fixed (acetone, formalin) frozen sections and found that less than 30% performed conservatively with all fixations, 35% preferred one fixation over another, 13% gave non-specific staining, 23% did not stain at all. Individual antibody variegation of the paratope fitness for the differentially fixed antigen may be the cause. Re-validation of established antibody panels is required when applied to sections whose fixation and processing is different from the tissue where they have been initially validated.





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