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3 protocols using alexa488 goat anti mouse secondary antibody

1

NF-κB p50 Subcellular Localization

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Nuclear and cytosol fractions were prepared using a Nuclear and Cytoplasmic Isolation kit (Thermo Scientific). All cells used for immunocytochemistry were fixed with 4% paraformaldehyde (Sigma) and permeabilized with 0.25% Trition X-100 in phosphate-buffered saline containing 1% bovine serum albumin. Fixed cells were incubated with an anti p50 (NF-κB) (1:500; SC-8414, RRID: AB_628015) antibody (Santa Cruz Biotechnology) at 4 °C overnight. After that, cells were incubated with Alexa 488 goat anti-mouse secondary antibody (Thermo Scientific) at 4 °C overnight. Images were obtained using an LSM-710 confocal microscope (Carl Zeiss, Oberkochen, Germany).
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2

Comprehensive Immunofluorescence Staining Assay

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Briefly, cells were fixed with 4% paraformaldehyde buffered in PBS for 10 min. Subsequently, the cells were permeabilized using PBS containing 0.5% Tween20 for 15 min. To block non-specific interactions, cells were incubated with 5% FBS in PBS for 1 hr. Lysosomes were stained using lysotracker deep red (Thermo Fisher Scientific) prior to fixation. Early endosomes were stained using Alexa 647conjugated anti-EEA1 (Abcam). PLY was stained using mouse anti-PLY (Abcam) and Alexa488-goat anti-mouse secondary antibody (Thermo Fisher Scientific). MRC-1 was detected using rabbit anti-MRC-1 (Abcam) and Alexa 555-goat anti-rabbit secondary antibody (Thermo Fisher Scientific). Pneumococci were stained using rabbit anti-pneumococcal anti-serum (Eurogentec) labeled with Alexa 488 using Zenon rabbit IgG labeling kit (Thermo Fisher Scientific). Type 1 clinical strains were stained using anti-serum Type 1 (Statens Serum Institut). Samples were washed twice with PBS between the antibody incubations and mounted on slides using ProLong Diamond antifade reagent containing DAPI (Thermo Fisher Scientific). Images were acquired using the Delta Vision Elite microscope under the 100x objective (GE Healthcare).
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3

Comprehensive Immunofluorescence Staining Assay

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Briefly, cells were fixed with 4% paraformaldehyde buffered in PBS for 10 min. Subsequently, the cells were permeabilized using PBS containing 0.5% Tween20 for 15 min. To block non-specific interactions, cells were incubated with 5% FBS in PBS for 1 hr. Lysosomes were stained using lysotracker deep red (Thermo Fisher Scientific) prior to fixation. Early endosomes were stained using Alexa 647conjugated anti-EEA1 (Abcam). PLY was stained using mouse anti-PLY (Abcam) and Alexa488-goat anti-mouse secondary antibody (Thermo Fisher Scientific). MRC-1 was detected using rabbit anti-MRC-1 (Abcam) and Alexa 555-goat anti-rabbit secondary antibody (Thermo Fisher Scientific). Pneumococci were stained using rabbit anti-pneumococcal anti-serum (Eurogentec) labeled with Alexa 488 using Zenon rabbit IgG labeling kit (Thermo Fisher Scientific). Type 1 clinical strains were stained using anti-serum Type 1 (Statens Serum Institut). Samples were washed twice with PBS between the antibody incubations and mounted on slides using ProLong Diamond antifade reagent containing DAPI (Thermo Fisher Scientific). Images were acquired using the Delta Vision Elite microscope under the 100x objective (GE Healthcare).
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