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Fitc conjugated antibody to mouse igg

Manufactured by Merck Group
Sourced in United States

FITC-conjugated antibody to mouse IgG is a fluorescently-labeled secondary antibody used for the detection and visualization of mouse primary antibodies in various immunoassays and histological applications.

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5 protocols using fitc conjugated antibody to mouse igg

1

Immunostaining of KB-VIN Cells

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Immunostaining of KB-VIN was performed as described previously.43 (link) Briefly, KB-VIN cells were seeded on an eight-well chamber slide (Lab-Tech) for 24 h prior to treatment with compounds. Cells were treated with compound for 24 h. Concentrations of reagents were used based on their IC50 used for cell cycle analysis as follows: 0.3 and 3.0 µM of 1, 20 µM 3, and 0.1% DMSO as a control. Cells were fixed in ice-cold 4% paraformaldehyde in phosphate-buffered saline (PBS) followed by permeabilization with 0.5% Triton X-100 in PBS. Fixed cells were labeled with mouse monoclonal antibody to α-tubulin (B5-1-2, Sigma) and rabbit polyclonal antibody to γ-H2AX (BETHYL Lab.) followed by FITC-conjugated antibody to mouse IgG (Sigma) and Alexa Fluor 546-conjugated antibody to rabbit IgG (Life Technologies). Nuclei were labeled with DAPI (Sigma). Fluorescence-labeled cells were observed using a confocal microscope (Zeiss, LSM700) controlled by ZEN software (Zeiss). Parameters (laser, beam splitter, band-pass filter) for confocal fluorescence imaging were used as follows: track 1 for DAPI (405 nm, 420 nm, 420−1000 nm), track 2 for FITC (488 nm, 544 nm, 490−555 nm), and track 3 for Alexa Fluor 546 (555 nm, 559 nm, 505−600 nm). Confocal images were reconstructed by stacking using ZEN (black edition) software (Zeiss). Final images were prepared by Photoshop CS6 (Adobe).
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2

Microscopic Imaging of α-Tubulin in MDA-MB-231 Cells

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MDA-MB-231 cells (2.4 × 104 cells/well) were grown on an 8-well chamber slide (Lab-Tech, Waltham, USA) for 24 h prior to treatment with reagents. Cells were treated for 24 h with compound 5 or DMSO as a control for 24 h. Cells were fixed in 4% paraformaldehyde in PBS and permeabilized with 0.5% Triton X-100 in PBS. Fixed cells were labeled with mouse monoclonal antibody to α-tubulin (B5-1-2, Sigma, St. Louis, MO, USA) followed by FITC-conjugated antibody to mouse IgG (Sigma) [31 (link)]. Nuclei were labeled with DAPI (Sigma). Fluorescence labeled cells were observed using confocal microscope (LSM700, Zeiss, White Plains, NY, USA) controlled by ZEN (black edition) software (Zeiss). Confocal images were stacked and merged using ZEN (black edition) software. Final images were prepared using Adobe Photoshop.
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3

Visualizing Microtubule Dynamics in MDA-MB-231 Cells

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MDA-MB-231 cells were seeded in the 8-well chamber slide (Lab-Tech) 24 h prior to treatment with compounds. After 24 h treatment, cells were fixed with 4% paraformaldehyde in PBS followed by permeabilization with 0.5% Triton-X100. Cells were then probed with antibody to α-tubulin (B5–1-2, Sigma) followed by FITC-conjugated antibody to mouse IgG (Sigma). Nuclei were labeled with 4′,6-diamidino-2-phenylindole (DAPI) (Sigma). Microtubules were detected using a confocal microscope (Zeiss, LSM700) controlled by ZEN software (Zeiss). Final images were reconstructed from 12−18 sections acquired at 0.6−1 μm intervals and merged using ZEN (black edition) software. Experiments were repeated at least twice for each compound at each concentration. Final images were prepared using Adobe Photoshop CS6.
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4

Immunofluorescence Microscopy of Tubulin

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KB-VIN cells (2.4 × 104 cells/well) were seeded
in an eight-well chamber slide (Lab-Tech)
for 24 h prior to treatment with compounds. The cells were treated
for 24 h with 2, 3, or DMSO as a control
for 24 h. Fixed (4% paraformaldehyde in PBS) and permeabilized (0.5%
Triton X-100 in PBS) cells were labeled with mouse monoclonal antibody
to α-tubulin (B5-1-2, Sigma), rabbit IgG to serine 10-phosphorylated
histone H3 (p-H3) (#06570, EMD Millipore) followed by FITC-conjugated
antibody to mouse IgG (Sigma) and Alexa Fluor 549-conjugated antibody
to rabbit IgG (Life Technologies).19 (link) Nuclei
were labeled with DAPI (Sigma). Fluorescence labeled cells were observed
using a confocal microscope (Zeiss, LSM700) controlled by ZEN software
(Zeiss). Confocal images of whole cells were superimposed and merged
using ZEN (black edition) software. Final images were prepared using
Adobe Photoshop CS6.
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5

Immunocytochemical Analysis of Microtubule and Mitotic Markers

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Immunocytochemical analysis was performed as previously described [26 (link)]. KB-VIN cells were grown on an 8-well chamber slide (Lab-Tech) for 24 h prior to treatment with the compound at a concentration of three-fold IC50. CA-4 was used at 0.2 μM (Figure 2A and Supporting Information, Supplementary Figure S1). After treatment of cells with the agent for 24 h, cells were fixed with 4% paraformaldehyde in PBS and permeabilized with 0.5% Triton X-100 in PBS. Fixed cells were labeled with mouse monoclonal antibody to α-tubulin (B5-1-2, Sigma) and rabbit IgG to Ser10-phosphorylated histone H3 (p-H3) (#06570, EMD Millipore), followed by FITC-conjugated antibody to mouse IgG (Sigma) and Alexa Fluor 549-conjugated antibody to rabbit IgG (Life Technologies). Nuclei were labeled with DAPI (Sigma). Fluorescently-labeled cells were observed using a confocal microscope (Zeiss, LSM700) with ZEN (black edition) software (Zeiss). The 15~20 optical sections acquired at 0.5~1 µm intervals were stacked and reconstructed using ZEN (black edition) software. Experiments were repeated at least twice for each compound. Final images were prepared using Adobe Photoshop CS3.
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