SpectraDye Antibody Labeling Kits – Witec AG

The labeling reaction really is fast and easy. Start by diluting antibody in PBS to 1 mg/ml.  Next, add 25 μl Antibody Labeling Buffer to 100 μl antibody solution. Mix thoroughly by pipetting up and down. Add 12 μl of Dye Solution to the reaction and mix by pipetting. Incubate 30 min at room temperature. Additional recommended steps: Add 3 μl Quenching Solution to the reaction mixture and incubate for 5 min at room temperature; then, add 8μl Neutralization Buffer to the reaction mixture. Antibody is labeled and ready to use.

Immunofluorescence Microscopy:

Decrease non-specific binding and eliminate species cross-reactivity when analyzing multiple antigens on the same slide.

Flow Cytometry: 

Simplify, decrease variability, and improve data quality in your flow cytometry assays by using your own fluorescently-labeled primary antibodies.

Western Blotting:

Save valuable time since secondary antibody incubation and wash steps are no longer required.

Increase the specificity of multicolor stained slides by using high quality monoclonal antibodies. HeLa cells were fixed on a glass coverslip then blocked with neutral donkey serum. The cells were then stained simultaneously with a panel of high-affinity SpectraDye labeled mouse monoclonal antibodies. The anti-GAPDH antibody was labeled with SpectraDye-490 (magenta), the anti-actin antibody was labeled with SpectraDye-650 (red) and the anti-tubulin antibody was labeled with SpectraDye-550 (green). The nuclei were stained with DAPI (blue).

SpectraDye Antibody Labeling Kits produce antibodies comparable to commercially available fluroescent antibodies. HeLa cells were cultured in DMEM medium supplemented with FBS and Penicillin/Streptomycin. The cells were pelleted and fixed with 4% paraformaldehyde. The HeLa cells were resuspended in PBS + 0.1% Triton and SpectraDye labeled antibodies were added at 0.33µg/µL. The antibodies were incubated at ambient temperature for 30 minutes then washed two times with 1X PBS. Data was acquired with the LSRFortessa. Black filled histogram represents antibody stained cells.  Black lined, gray histogram represents the unstained control.

Detect two or more proteins in a single fluorescent Western blot experiment using SpectraDye-labeled primary antibodies. Transferrin (500ng/lane) and GAPDH (500, 167, 56, and 19 ng/lane) were transferred to a PVDF membrane and detected with a rabbit anti-transferrin antibody labeled with SpectraDye-IR800 and a mouse anti-GAPDH antibody labeled with SpectraDye-IR700.