El-Hajj et al. Page 2 We report here the use of novel "sloppy " molecular beacon probes in homogeneous PCR screening assays, in which thermal denaturation of the resulting probe-amplicon hybrids provides a characteristic set of Tm values that identify which species is present in a sample. Sloppy molecular beacons possess relatively long probe sequences, enabling them to form hybrids with amplicons from many different species, despite the presence of mismatched basepairs. By using four sloppy molecular beacons, each possessing a different probe sequence, and each labeled with a differently colored fluorophore, four different Tm values can be determined simultaneously. We tested this technique with 27 different species of mycobacter...
Mycobacterium chimaera is an opportunistic environmental mycobacterium belonging to the Mycobacteriu...
A real-time polymerase chain reaction (PCR) assay for the direct identification of Mycobacterium tub...
Marme N, Friedrich A, Müller M, et al. Identification of single-point mutations in mycobacterial 16S...
We report here the use of novel “sloppy ” molecular beacon probes in homogeneous PCR screening assay...
Stohr K, Hafner B, Nolte O, Wolfrum J, Sauer M, Herten DP. Species-specific identification of mycoba...
A real-time PCR assay with the ability to rapidly identify all pathogenic bacteria would have widesp...
Although commercially available DNA probes for identification of mycobacteria have been investigated...
We developed a new approach to DNA sequence analysis that uses fluorogenic reporter molecules--molec...
Although commercially available DNA probes for identification of mycobacteria have been investigated...
AIMS: To develop a real-time PCR method for rapid differential identification of many clinically imp...
Species identification within the genus Mycobacterium and subsequent antibiotic susceptibility testi...
The number of different fluorescent colors that can be distinguished in a PCR screening assay restri...
identification, by means of reverse hybridization and line-probe technology, of Mycobacterium tuberc...
Detection of multidrug-resistant tuberculosis (MDR-TB), a frequent cause of treatment failure, takes...
Abstract Background Our ultimate goal is to detect the entire human microbiome, in health and in dis...
Mycobacterium chimaera is an opportunistic environmental mycobacterium belonging to the Mycobacteriu...
A real-time polymerase chain reaction (PCR) assay for the direct identification of Mycobacterium tub...
Marme N, Friedrich A, Müller M, et al. Identification of single-point mutations in mycobacterial 16S...
We report here the use of novel “sloppy ” molecular beacon probes in homogeneous PCR screening assay...
Stohr K, Hafner B, Nolte O, Wolfrum J, Sauer M, Herten DP. Species-specific identification of mycoba...
A real-time PCR assay with the ability to rapidly identify all pathogenic bacteria would have widesp...
Although commercially available DNA probes for identification of mycobacteria have been investigated...
We developed a new approach to DNA sequence analysis that uses fluorogenic reporter molecules--molec...
Although commercially available DNA probes for identification of mycobacteria have been investigated...
AIMS: To develop a real-time PCR method for rapid differential identification of many clinically imp...
Species identification within the genus Mycobacterium and subsequent antibiotic susceptibility testi...
The number of different fluorescent colors that can be distinguished in a PCR screening assay restri...
identification, by means of reverse hybridization and line-probe technology, of Mycobacterium tuberc...
Detection of multidrug-resistant tuberculosis (MDR-TB), a frequent cause of treatment failure, takes...
Abstract Background Our ultimate goal is to detect the entire human microbiome, in health and in dis...
Mycobacterium chimaera is an opportunistic environmental mycobacterium belonging to the Mycobacteriu...
A real-time polymerase chain reaction (PCR) assay for the direct identification of Mycobacterium tub...
Marme N, Friedrich A, Müller M, et al. Identification of single-point mutations in mycobacterial 16S...