from duplicate 1.8 ml C. albicans cultures was isolated with the QIAamp PowerFecal DNA (A) or the QIAamp PowerFecal
Pro DNA (B) Kits. B, C DNA from stool samples (200 mg) from three donors was prepared with the first-generation QIAamp
PowerFecal DNA Kit B or the new QIAamp PowerFecal Pro DNA Kit C. DNA was analyzed via gel electrophoresis.
Stool samples (200 mg) were prepared using commercially available sample preparation solutions or the new QIAamp PowerFecal Pro DNA Kit and compared. DNA purity was measured via UV spectrophotometry and the comparisons of A260/A280A and A260/A230B ratios are shown.
prepared from stool samples was isolated with different
methods and enriched. Analysis of the 16S rRNA genes was done using the QIAseq® 1-Step Amplicon Kit and data
analysis was done using the Microbial Genomics Pro DNA
Suite (CLC workbench). Alpha diversity was determined by
total number of bacterial OTUs.
DNA was isolated from stool samples (200 mg) from three donors using commercially available sample preparation solutions and the new QIAamp PowerFecal Pro DNA Kit and compared. Yields were measured by fluorometric quantification (Qubit™).