Non-infected (–) and infected (+) C6/36 whole cell extracts (30 μg) were separated by 15% SDS-PAGE, and the membrane was blotted with Zika virus prM protein antibody (GTX133305) diluted at 1:2000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.

Non-infected (–) and infected (+) Vero cells (15 μg) were separated by gradient gel, and the membrane was blotted with Zika PrM antibody (GTX133305) diluted at 1:2000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.

Immunofluorescent analysis of arboviruses infected cells using Zika virus prM protein antibody (GTX133305).
Samples: EUROIMMUN Arboviral Fever Mosaic 2 slide (FR 2668-1010-1).
Green: Zika virus prM protein antibody (GTX133305) diluted at 1:500.
Blue: Hoechst 33342 staining.
Scale bar = 10 μm.

The data was published in the journal PLoS Negl Trop Dis in 2017.PMID: 28481898