Literature DB >> 21140588

Fluorescent in situ hybridization heating pretreatment: the key is temperature control.

Marta Tojo1, Elena Couso, Angel Vázquez-Boquete, Raquel Pérez-Becerra, Tomás García-Caballero, Jerónimo Forteza, Máximo Fraga.   

Abstract

Fluorescent in situ hybridization (FISH) is a very useful tool for diagnostic and prognostic purposes in pathology. However, many laboratories still experience troubles when applying FISH to paraffin material. To overcome these difficulties, different pretreatments which include enzymatic digestion have been described. Usually, previous to digestion, a heating step is performed. The aim of this study was to compare the efficiency of the heating step with different buffers and different heating methods. We conclude that the main factor in the heating pretreatment is the temperature control, irrespective of the buffer used. Best results are obtained with any buffer by heating the slides to 99°C for 15 min followed by 10 min at room temperature.

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Year:  2010        PMID: 21140588     DOI: 10.1111/j.1440-1827.2010.02600.x

Source DB:  PubMed          Journal:  Pathol Int        ISSN: 1320-5463            Impact factor:   2.534


  2 in total

1.  A new method for real-time evaluation of pepsin digestion of paraffin-embedded tissue sections, prior to fluorescence in situ hybridisation.

Authors:  Xiaojing Teng; Shuhong Zhang; Wei Liu; Kuo Bi; Lei Zhang
Journal:  Virchows Arch       Date:  2017-02-25       Impact factor: 4.064

2.  One-fits-all pretreatment protocol facilitating Fluorescence In Situ Hybridization on formalin-fixed paraffin-embedded, fresh frozen and cytological slides.

Authors:  Shivanand O Richardson; Manon M H Huibers; Roel A de Weger; Wendy W J de Leng; John W J Hinrichs; Ruud W J Meijers; Stefan M Willems; Ton L M G Peeters
Journal:  Mol Cytogenet       Date:  2019-06-17       Impact factor: 2.009

  2 in total

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