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Ar 441 pan ar antibody

Manufactured by Santa Cruz Biotechnology

The AR-441 pan-AR antibody is a laboratory research tool designed to detect androgen receptor (AR) protein expression in biological samples. It is a polyclonal antibody that recognizes multiple isoforms of the AR protein, making it a useful tool for studying AR expression in various cell and tissue types. The core function of this antibody is to provide a reliable and specific method for the detection and analysis of AR proteins in research applications.

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2 protocols using ar 441 pan ar antibody

1

Immunofluorescence Quantification of AR-V7

Check if the same lab product or an alternative is used in the 5 most similar protocols
After fixation with 4% paraformaldehyde, cells were incubated with an anti-FLAG (for cumate-inducible AR-V7-expressing LNCaP cells; Sigma-Aldrich, F3165) or AR-441 pan-AR antibody (for PC-3 cells transfected with AR-V7; Santa Cruz Biotechnology, sc-7305) overnight at 4°C and then washed and incubated with Alexa Fluor 488-conjugated secondary antibody (Thermo Fisher, A-11001) for 1 hr at room temperature in the dark and counterstained with DAPI. An average of 10 fields were captured for each group using a Nikon A1r confocal fluorescence microscope. The intensity ratios of nuclear and cytoplasmic fluorescence signals were quantitated using ImageJ.
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2

Immunofluorescence Quantification of AR-V7

Check if the same lab product or an alternative is used in the 5 most similar protocols
After fixation with 4% paraformaldehyde, cells were incubated with an anti-FLAG (for cumate-inducible AR-V7-expressing LNCaP cells; Sigma-Aldrich, F3165) or AR-441 pan-AR antibody (for PC-3 cells transfected with AR-V7; Santa Cruz Biotechnology, sc-7305) overnight at 4°C and then washed and incubated with Alexa Fluor 488-conjugated secondary antibody (Thermo Fisher, A-11001) for 1 hr at room temperature in the dark and counterstained with DAPI. An average of 10 fields were captured for each group using a Nikon A1r confocal fluorescence microscope. The intensity ratios of nuclear and cytoplasmic fluorescence signals were quantitated using ImageJ.
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