Literature DB >> 9375292

Construction and use of PCR primers from a 70 kDa heat shock protein gene for identification of Candida albicans.

S Arancia1, S Sandini, A Cassone, F De Bernardis, R La Valle.   

Abstract

Methods for detection of Candida albicans in culture or biological samples were developed by the use of polymerase chain reaction (PCR) with oligonucleotide primers from C. albicans 70 kDa heat shock protein gene (Cahsp70). The PCR amplifies a 335-base pair fragment which is then hybridized with a non-radioactive probe, leading to the specific identification of C. albicans and its differentiation from all other human pathogenic Candida and/or yeast species. Candida albicans could be rapidly detected in human urine and blood, with a sensitivity of 10 and 50 fungal cells per sample, respectively.

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Year:  1997        PMID: 9375292     DOI: 10.1006/mcpr.1997.0125

Source DB:  PubMed          Journal:  Mol Cell Probes        ISSN: 0890-8508            Impact factor:   2.365


  2 in total

1.  Contaminations occurring in fungal PCR assays.

Authors:  J Loeffler; H Hebart; R Bialek; L Hagmeyer; D Schmidt; F P Serey; M Hartmann; J Eucker; H Einsele
Journal:  J Clin Microbiol       Date:  1999-04       Impact factor: 5.948

2.  Comparison of non-culture-based methods for detection of systemic fungal infections, with an emphasis on invasive Candida infections.

Authors:  P Lewis White; Alice E Archer; Rosemary A Barnes
Journal:  J Clin Microbiol       Date:  2005-05       Impact factor: 5.948

  2 in total

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