Determination of 1g antibodies produced by the kinetoplast fraction antigens trypanosoma rhodesiense T.Vivax and T. brucei by enzyme linked immunosorbent assay

dc.contributor.authorPowell, C. N
dc.contributor.authorMohini, A.
dc.date.accessioned2019-06-17T15:33:10Z
dc.date.available2019-06-17T15:33:10Z
dc.date.issued1977-04
dc.descriptionAntibodies to trypanosome homegenate and subcellular particles of different trypanosome species, with emphasis on the kinetoplast fraction.en
dc.description.abstractAntibodies to trypanosome homegenate and subcellular particles of different trypanosome species, with emphasis on the kinetoplast fraction, were measured by the ELISA method. The antibodies formed to these homogenates and subcellular particles could be titrated ; the kinetoplast fraction, particularly, not only gave titration against a heterologous strain, but also showed activity against this strain after two to three antigenic variations.en
dc.description.sponsorshipOffice of Global AIDS/US Department of State.en
dc.identifier.citationPowell, C. N. and Mohini, A. ((1977). Determination of 1g antibodies produced by the kinetoplast fraction antigens trypanosoma rhodesiense T.Vivax and T. brucei by enzyme linked immunosorbent assay. Medical Journal of Zambia. 11, (2)en
dc.identifier.urihttp://dspace.unza.zm/handle/123456789/5970
dc.language.isoenen
dc.publisherMedical Journal of Zambia.en
dc.relation.ispartofseriesVol.11;No.2
dc.subjectKinetoplast Fractionen
dc.subjectEnzyme linked lmmunosorbent Assayen
dc.titleDetermination of 1g antibodies produced by the kinetoplast fraction antigens trypanosoma rhodesiense T.Vivax and T. brucei by enzyme linked immunosorbent assayen
dc.typeArticleen
Files
Original bundle
Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
MJZ;VOL11;2;APR-MAY1977_ lmmunosorbent.pdf
Size:
401.69 KB
Format:
Adobe Portable Document Format
Description:
Journal Article
License bundle
Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
license.txt
Size:
1.72 KB
Format:
Item-specific license agreed upon to submission
Description: