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. 2011 Jun;85(12):5919–5928. doi: 10.1128/JVI.00116-11

Table 1.

Colocalization of fluorescence in YK614 virus particles from cell culture supernatants of Vero cellsa

Fluorescence Colocalizationb
mRFP-gB 221/276 (80)
R#68 (rabbit polyclonal anti-gB) 152/210 (72)
DL6 (mouse anti-gD MAb) 165/211 (78)
3B6 and H1.4 (anti-VP5 MAb) 222/263 (84)
NC-1 (rabbit polyclonal anti-VP5) 197/225 (88)
NC-7 (rabbit polyclonal anti-VP26) 178/198 (90)
a

YK614 (expressing both mRFP-gB and VP26-Venus) particles from cell culture supernatants were allowed to adhere to polylysine- and laminin-coated glass coverslips; then they were fixed with 4% PFA and permeabilized with 0.2% Triton X-100 before being imaged directly (VP26-Venus versus mRFP-gB) or stained with various antibodies.

b

Expressed as the number of capsids detected by VP26-Venus fluorescence that exhibited mRFP-gB fluorescence or stained with the anti-gB, anti-gD, anti-VP5, or anti-VP26 antibodies/total number of capsids detected by VP26-Venus fluorescence (percentage).