<p>WT 8004 cells (Panels A and C) and 8004Δ<i>dltA</i> cells (Panels B and D) were stained either with human anti-C3 (Panels A and B) or anti-M1 (Panels C and D) antibodies. DAPI staining (blue) was used to visualize nuclei. Note that the fluorescence associated with M proteins (red) decreases in the <i>dltA</i> mutant and the fluorescence associated with C3 dramatically increases (green).</p
<p>Cells were stained either with a relevant isotype-matched control antibody (isotype) or with an H...
<p>A) Immunofluorescence and wide-field epifluorescence microscopy on human cells with; (upper row) ...
<p>Immunofluorescent based comparison of the sub-cellular distribution of wt JCV T-ag, and the F258L...
<p>WT bacteria (open histogram) and Δ<i>dltA</i> mutants (filled histogram) were stained with a fluo...
Shown are plain HL-1, cells stably overexpressing wildtype of hCD36, and mutant-2, as indicated. Cel...
<p>(A) A merged image of bright field and C-1371 green fluorescence in live MCF-7/MR cells before il...
<p>mERα expression (green fluorescence) in unpermeated SH-SY5Y cells and MAP2 expression (red fluore...
<p>HCV29, KK47, and YTS1 cells were cultured and stained with six antibodies directed to identified ...
<p>The indicated cells were fixed, permeabilized and stained for immunofluorescence microscopy using...
<p>Cells were grown on coverslips and stained with anti-TMEM16A antibodies. Left column, anti-TMEM16...
<p>The cell lines HVBP (A) and HMEC-1 (B) were stained with selected M3-H12 antibody and detected wi...
<p>To visualize degradation of mucin-type glycoproteins by SPATEs, Jurkat T cells were treated with ...
<p>Confocal images showing cytoplasmic localization of cytokeratin-13(green) in hPVECs (a-c) and VK2...
<p><b>A–C</b>. Cos7 cells were treated with DMSO (A) or treated with 5 µM MG132 for 16 hours (B–C) a...
<p>BeWo cells grown on (A) 2D, (B) thin Matrigel, or (C) thick Matrigel surfaces. Green fluorescence...
<p>Cells were stained either with a relevant isotype-matched control antibody (isotype) or with an H...
<p>A) Immunofluorescence and wide-field epifluorescence microscopy on human cells with; (upper row) ...
<p>Immunofluorescent based comparison of the sub-cellular distribution of wt JCV T-ag, and the F258L...
<p>WT bacteria (open histogram) and Δ<i>dltA</i> mutants (filled histogram) were stained with a fluo...
Shown are plain HL-1, cells stably overexpressing wildtype of hCD36, and mutant-2, as indicated. Cel...
<p>(A) A merged image of bright field and C-1371 green fluorescence in live MCF-7/MR cells before il...
<p>mERα expression (green fluorescence) in unpermeated SH-SY5Y cells and MAP2 expression (red fluore...
<p>HCV29, KK47, and YTS1 cells were cultured and stained with six antibodies directed to identified ...
<p>The indicated cells were fixed, permeabilized and stained for immunofluorescence microscopy using...
<p>Cells were grown on coverslips and stained with anti-TMEM16A antibodies. Left column, anti-TMEM16...
<p>The cell lines HVBP (A) and HMEC-1 (B) were stained with selected M3-H12 antibody and detected wi...
<p>To visualize degradation of mucin-type glycoproteins by SPATEs, Jurkat T cells were treated with ...
<p>Confocal images showing cytoplasmic localization of cytokeratin-13(green) in hPVECs (a-c) and VK2...
<p><b>A–C</b>. Cos7 cells were treated with DMSO (A) or treated with 5 µM MG132 for 16 hours (B–C) a...
<p>BeWo cells grown on (A) 2D, (B) thin Matrigel, or (C) thick Matrigel surfaces. Green fluorescence...
<p>Cells were stained either with a relevant isotype-matched control antibody (isotype) or with an H...
<p>A) Immunofluorescence and wide-field epifluorescence microscopy on human cells with; (upper row) ...
<p>Immunofluorescent based comparison of the sub-cellular distribution of wt JCV T-ag, and the F258L...