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Fluorescein conjugated secondary antibody fitc 1 150

Manufactured by Vector Laboratories

Fluorescein-conjugated secondary antibody (FITC 1:150) is a laboratory reagent used to detect and visualize primary antibodies in immunoassays. The antibody is conjugated with the fluorescent dye fluorescein isothiocyanate (FITC), which emits green fluorescence when excited by an appropriate light source.

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2 protocols using fluorescein conjugated secondary antibody fitc 1 150

1

Immunofluorescence Characterization of T-47D Cells

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T-47D cells were grown on coverslips. Cells were fixed with 4% paraformaldehyde for 30 min and permeabilized with 0.1% Triton for 5 min. Blocking was performed with PBS containing 3% bovine serum albumin for 30 min at room temperature. Cells were incubated with antibodies against p-paxillinY118; vimentin (E-5) (Santa Cruz Biotechnology); E-cadherin (24E10) (Cell Signaling Technology); p-N-WASPS484/485 (Chemicon International); and p-Arp2T237 (Biorbyt) overnight at 4 °C, followed by incubation with DyLight488/ DyLight594 and/or fluorescein-conjugated secondary antibody (FITC 1:150; Vector Laboratories, Burlingame, CA). Cells were then incubated with Texas Red-phalloidin (Sigma-Aldrich, Saint-Louis, MO) for 30 min. After washing, the nuclei were counterstained with or 4'-6-diamidino-2-phenylindole (DAPI) (Sigma-Aldrich, Saint-Louis, MO) and mounted with Vectashield mounting medium (Vector Laboratories, Burlingame, CA). Immunofluorescence was visualized using a Nikon Eclipse E200 microscope and recorded with a high-resolution DP70 Olympus digital camera.
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2

Immunofluorescence Analysis of Cytoskeletal Proteins

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T-47D cells were grown on coverslips and exposed to different treatments. Cells were fixed with 4% paraformaldehyde for 30 min and permeabilized with 0.1% Triton for 5 min. Blocking was performed with phosphate-buffered saline (PBS) containing 3% bovine serum albumin (BSA) for 30 min at room temperature. Cells were incubated with antibodies against p-N-WASPS484/485 (Chemicon International) and p-paxillinY118 and p-cortactinY466 (Santa Cruz Biotechnology) overnight at 4°C, followed by incubation with DyLight 594 and/or fluorescein-conjugated secondary antibody (FITC 1:150; Vector Laboratories). Cells were then incubated with Texas Red–phalloidin (Sigma-Aldrich) for 30 min. After washing, the nuclei were counterstained with 4’-6-diamidino-2-phenylindole (DAPI) (Sigma-Aldrich) and mounted with VECTASHIELD mounting medium (Vector Laboratories, Burlingame, CA). Immunofluorescence was visualized using a Nikon Eclipse E200 microscope and recorded with a high-resolution DP70 Olympus digital camera.
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