Exact(1)
After drying the cell pellet in a desiccator over night in vacuo, PCP (Phenol-Chloroform-petroleum ether) method was used for rough LPS extraction (Galanos et al., 1969).
Similar(59)
The study participants were asked to provide weekly fecal specimens for microscopic detection of ova and parasites, including Cryptosporidium spp. Stool specimens were washed and concentrated by using the modified Ritchie formalin-ether method and examined for Cryptosporidium spp. oocysts by microscopy of smears stained with a modified acid-fast stain.
Saline wet mount and Lugols Iodine mount was done by direct microscopy and a formalin ether concentration method to detect ova, trophozoites, cysts, and larvae of intestinal parasites.
The formol-ether concentration method was performed on 50% of the samples to confirm results obtained by the Kato-Katz technique [55].
The formol-ether concentration method was performed on a random sample of 25% of the samples to confirm results obtained by the Kato-Katz technique.
The detection limit of the assay with the ether-extraction method is approximately.05 nmol/L.
Stool samples were examined for the presence of parasites using direct, formal-ether concentration method and the Modified Ziehl Neelsen staining technique.
Cryptosporidium oocysts were identified by light microscopy after concentration from fecal material by a modified water-ether sedimentation method followed by the modified Ziehl-Neelsen staining (7 ).
Additionally, all faecal samples were examined qualitatively using the modified formol-ether concentration method to ascertain the child's intestinal parasites infection status.
A total of 768 stool specimens were collected and examined for intestinal parasites using direct wet mount with saline and formalin ether concentration methods.
Fecal samples were processed by the acid-ether concentration method and then examined by microscopy to identify the presence of protozoan cysts and helminth eggs (6 ).
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