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We used only purified clonal bacterial isolates, and did not need to perform isolations from patient derived samples.
SN performed isolation and identification of isolates, molecular typing and susceptibility testing, analyzed the data and drafted the manuscript.
To determine whether dissemination might be an event associated with imminent death of an embryo, we additionally performed isolation from livers and complete abdomens of freshly deceased embryos.
LRM performed isolation of mitochondria and purification of mitochondrial DNA.
MJAS and AS performed isolation of active compound.
TD performed isolation and microbiological identification of bacteria.
BDJ performed isolation, distribution and sequence characterization of pBJS-O.
JH performed isolation and characterization of tissue samples and assembly of patients.
We performed isolation and cloning of the VvCCD4a gene into pGEX expression vector.
DB performed isolation and culture of HUVEC, measure ATP LDH and protein levels in HUVEC.
JA and BR performed isolation and culture of peripheral blood EPC-derived endothelial cells and supplied clinical data.
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