A Novel System for Rapid and Cost-Effective Production of Detection and Diagnostic Reagents of West Nile Virus in Plants

<table>Purification of E16 mAbs produced in lettuce or <i>N. benthamiana</i>. Purified E16 mAbs were analyzed on a 12% SDS-PAGE gel using either reducing (Lanes 2–4) or nonreducing (Lanes 5–7) sample buffer. Lane 1: Molecular weight marker; lanes 2 and 5: mammalian cell-derived E16 as reference standard; lanes 3 and 6: E16 purified from lettuce leaves; lanes 4 and 7: purified E16 from <i>N. benthamiana. </i>One representative of several independent experiments is shown.</table>

BioMed Research International

fig3

Figure 3

Figure 3: A Novel System for Rapid and Cost-Effective Production of Detection and Diagnostic Reagents of West Nile Virus in Plants 