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dc.contributor.advisorClinkenbeard, Kenneth D.
dc.contributor.authorMani, Rinosh Joshua
dc.date.accessioned2014-04-16T03:15:58Z
dc.date.available2014-04-16T03:15:58Z
dc.date.issued2006-07-01
dc.identifier.urihttps://hdl.handle.net/11244/9821
dc.description.abstractUsing the bi-cell surface plasmon resonance instrument, we were able to detect thrombin in the concentration range of 500 femtomoles to 2 picomoles with thrombin aptamer as the capture probe. The lowest limit of detection was 250 femtomoles. The affinity of the aptamer for prothrombin was also investigated, which was detected at 2 picomoles. Using serum samples, 1 picomole of thrombin was detected. We proved that an aptamer could be used as a capture ligand in bi-cell SPR instrument. This model could be used in a clinical setting for the real time detection of diagnostically relevant biomolecules.
dc.formatapplication/pdf
dc.languageen_US
dc.publisherOklahoma State University
dc.rightsCopyright is held by the author who has granted the Oklahoma State University Library the non-exclusive right to share this material in its institutional repository. Contact Digital Library Services at lib-dls@okstate.edu or 405-744-9161 for the permission policy on the use, reproduction or distribution of this material.
dc.titleApplication of Bi-cell Surface Plasmon Resonance for the Detection of Aptamer Mediated Thrombin Capture in Serum
dc.typetext
dc.contributor.committeeMemberMeinkoth, James H.
dc.contributor.committeeMemberMorton, Rebecca J.
osu.filenameMani_okstate_0664M_1949.pdf
osu.collegeCenter for Veterinary Health Sciences
osu.accesstypeOpen Access
dc.description.departmentVeterinary Pathobiology
dc.type.genreThesis


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