sybr-green-i and Irritable-Bowel-Syndrome

sybr-green-i has been researched along with Irritable-Bowel-Syndrome* in 1 studies

Other Studies

1 other study(ies) available for sybr-green-i and Irritable-Bowel-Syndrome

Article	Year
Development of an extensive set of 16S rDNA-targeted primers for quantification of pathogenic and indigenous bacteria in faecal samples by real-time PCR. Journal of applied microbiology, 2004, Volume: 97, Issue:6 The microbiota of the human intestinal tract constitutes a complex ecosystem. We report the design and optimization of an extensive set of 16S rDNA-targeted species- and group-specific primers for more accurate quantification of bacteria from faecal samples with real-time PCR.. A linear range of quantification between 0.1-10 pg and 10 ng of specific target genome was obtained, which corresponds to detection of ca 30-4500 to 1.9 x 10(6)-6.0 x 10(6) target bacterial genomes. Functionality of the assays was confirmed by quantification of target bacterial DNA from faecal DNA preparations of healthy volunteers and irritable bowel syndrome (IBS) patients. Additionally, spiking of faecal preparations with Helicobacter pylori, Clostridium difficile or Campylobacter jejuni was used to confirm the accurate and sensitive quantification.. Real-time PCR is a very sensitive and precise technique for an extensive quantitative evaluation of gut microbiota and is feasible for detection of human pathogens from faecal samples.. To design and optimize an extensive set of real-time PCR assays targeting a large group of predominant and pathogenic GI microbial species for further use in updating the current knowledge of the putative role of gut microbiota in health and disease. Topics: Adult; Bacteria; Base Sequence; Benzothiazoles; Clostridium; Diamines; DNA Primers; DNA, Bacterial; DNA, Ribosomal; Escherichia coli; Feces; Fluorescent Dyes; Genome, Bacterial; Helicobacter pylori; Humans; Irritable Bowel Syndrome; Organic Chemicals; Polymerase Chain Reaction; Quinolines; Species Specificity	2004

Article

Year

Development of an extensive set of 16S rDNA-targeted primers for quantification of pathogenic and indigenous bacteria in faecal samples by real-time PCR.

Journal of applied microbiology, 2004, Volume: 97, Issue:6

The microbiota of the human intestinal tract constitutes a complex ecosystem. We report the design and optimization of an extensive set of 16S rDNA-targeted species- and group-specific primers for more accurate quantification of bacteria from faecal samples with real-time PCR.. A linear range of quantification between 0.1-10 pg and 10 ng of specific target genome was obtained, which corresponds to detection of ca 30-4500 to 1.9 x 10(6)-6.0 x 10(6) target bacterial genomes. Functionality of the assays was confirmed by quantification of target bacterial DNA from faecal DNA preparations of healthy volunteers and irritable bowel syndrome (IBS) patients. Additionally, spiking of faecal preparations with Helicobacter pylori, Clostridium difficile or Campylobacter jejuni was used to confirm the accurate and sensitive quantification.. Real-time PCR is a very sensitive and precise technique for an extensive quantitative evaluation of gut microbiota and is feasible for detection of human pathogens from faecal samples.. To design and optimize an extensive set of real-time PCR assays targeting a large group of predominant and pathogenic GI microbial species for further use in updating the current knowledge of the putative role of gut microbiota in health and disease.

Topics: Adult; Bacteria; Base Sequence; Benzothiazoles; Clostridium; Diamines; DNA Primers; DNA, Bacterial; DNA, Ribosomal; Escherichia coli; Feces; Fluorescent Dyes; Genome, Bacterial; Helicobacter pylori; Humans; Irritable Bowel Syndrome; Organic Chemicals; Polymerase Chain Reaction; Quinolines; Species Specificity

2004