Literature DB >> 8576298

Automated detection of digoxigenin-labelled B19 parvovirus amplicons by a capture hybridization assay.

M Zerbini1, D Gibellini, M Musiani, S Venturoli, G Gallinella, G Gentilomi.   

Abstract

An automated method to identify B19 amplicons, directly labelled with digoxigenin during amplification reaction was developed. The labelled amplicons were hybridized with a biotinylated B19 oligo-probe and captured on commercially available test tubes coated with streptavidin. The hybridized amplicons labelled with digoxigenin were detected using anti-digoxigenin Fab fragments conjugated to peroxidase and the colourimetric reaction automatically evaluated as an immunoenzymatic assay. Fifty serum samples were tested by the assay and the results were in accordance with those obtained by Southern blot analysis of amplified products. Due to the high sensitivity, specificity and reproducibility shown, the assay seems to be a practical and reliable test for the diagnosis of B19 infection and can be easily adapted to identify any digoxigenin-labelled amplified product of viral genomes.

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Year:  1995        PMID: 8576298     DOI: 10.1016/0166-0934(95)00038-v

Source DB:  PubMed          Journal:  J Virol Methods        ISSN: 0166-0934            Impact factor:   2.014


  4 in total

1.  Quantitative direct probe method for the detection of parvovirus B19.

Authors:  H Boggino; D A Payne
Journal:  J Clin Lab Anal       Date:  2000       Impact factor: 2.352

2.  Evaluation of immunoassays for the detection and typing of PCR amplified human papillomavirus DNA.

Authors:  S Venturoli; M Zerbini; M La Placa; A D'Antuono; M Negosanti; G Gentilomi; G Gallinella; E Manaresi; M Musiani
Journal:  J Clin Pathol       Date:  1998-02       Impact factor: 3.411

3.  High-sensitivity PCR detection of parvovirus B19 in plasma.

Authors:  P Daly; A Corcoran; B P Mahon; S Doyle
Journal:  J Clin Microbiol       Date:  2002-06       Impact factor: 5.948

4.  Quantitative competitive-PCR assay to measure human parvovirus B19-DNA load in serum samples.

Authors:  Massimiliano Bergallo; Chiara Merlino; Roberta Daniele; Cristina Costa; Alessandro Negro Ponzi; Rossana Cavallo
Journal:  Mol Biotechnol       Date:  2006-01       Impact factor: 2.695

  4 in total

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