1986
DOI: 10.1016/0014-4894(86)90195-5
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Entamoeba histolytica: Specific antigen recognized by a monoclonal antibody

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Cited by 9 publications
(8 citation statements)
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“…The ELISA method used in this work showed that the monoclonal anti-E. histolytica could detect the presence of amoebic antigen in fecal samples and was sufficiently sensitive to detect 0.1 pg of this antigen or ten or more E. histolytica trophozoites. As stated in Materials and Methods, this monoclonal antibody has been shown to have the necessary specificity to distinguish between E. histolytica and other Entamoeba species (8). This specificity was also demonstrated here by the lack of reactivity with the other parasites, especially Entamoeba coli, with which Entamoeba histolytica is often confused.…”
Section: Discussionsupporting
confidence: 69%
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“…The ELISA method used in this work showed that the monoclonal anti-E. histolytica could detect the presence of amoebic antigen in fecal samples and was sufficiently sensitive to detect 0.1 pg of this antigen or ten or more E. histolytica trophozoites. As stated in Materials and Methods, this monoclonal antibody has been shown to have the necessary specificity to distinguish between E. histolytica and other Entamoeba species (8). This specificity was also demonstrated here by the lack of reactivity with the other parasites, especially Entamoeba coli, with which Entamoeba histolytica is often confused.…”
Section: Discussionsupporting
confidence: 69%
“…That this monoclonal antibody is specific to strains of E. histolyticu has been demonstrated (8). In an ELISA, this monoclonal antibody was shown to react with soluble antigen from E. histolyticu strains HM1 :IMSS, HM3:IMSS, HM38:IMSS, and HK9:NIH but not from E. moshkovskii, E, invadens, or E. histolyticu-related Laredo strain.…”
Section: Preparation Of Fecal Samplesmentioning
confidence: 93%
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“…The method is based on an enzyme-linked immunosorbent assay (ELISA) technique in which we use a monoclonal antibody (C29) directed against one of the E. histolytica surface molecules (Ortiz-Ortiz et al 1986). Optimal conditions for amebic adhesion to monolayers of MDCK cells in 96-well culture plates were the following: incubation of 5´10 4 trophozoites/microwell in 200 ll of 2.0 mM PBS (pH 5.7) by coincubation for 15 min at 37°C with gentle shaking (75 rpm).…”
Section: Study Of Amebic Adhesion To Monolayers Of Mdck Cellsmentioning
confidence: 99%
“…A well-defined monoclonal antibody, specific for E. histolytica (12), was employed for the ELISA technique. In brief, each fecal sample was homogenized in 0.01 M phosphate buffer containing 0.15 M NaCl (PBS), pH 7.4, which contained sodium dodecyl sulfate (0.05%), and added on wells of polystyrene previously coated with 10 pg of polyclonal anti-E. histolytica (100 pl) in 0.1 M carbonate buffer, pH 9.6.…”
Section: Elsa Techniquementioning
confidence: 99%