Anti-Androgen receptor/AR Antibody

筛选器： All WB FCM ICC/IF ELISA

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  Western blot analysis of Androgen receptor/AR using anti-Androgen receptor/AR antibody (A00542). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
  Lane 1: Human K562 whole cell lysates,
  Lane 2: Human U2OS whole cell lysates,
  Lane 3: Human HEK293 whole cell lysates,
  Lane 4: Human PC-3 whole cell lysates,
  Lane 5: Human 22RV1 whole cell lysates,
  Lane 6: Human HepG2 whole cell lysates,
  Lane 7: Human CACO-2 whole cell lysates.
  After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-Androgen receptor/AR antigen affinity purified polyclonal antibody (A00542) at a dilution of 1:1000 and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for Androgen receptor/AR at approximately 110-120 kDa. The expected band size for Androgen receptor/AR is at 99 kDa.

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  Flow Cytometry analysis of A549 cells using anti-Androgen receptor/AR antibody (A00542).
  Overlay histogram showing A549 cells stained with A00542 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Androgen receptor/AR Antibody (A00542) at 1:100 dilution for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG at 1:100 dilution used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.

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  Flow Cytometry analysis of C6 cells using anti-Androgen receptor/AR antibody (A00542).
  Overlay histogram showing C6 cells stained with A00542 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Androgen receptor/AR Antibody (A00542) at 1:100 dilution for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG at 1:100 dilution used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.

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  Flow Cytometry analysis of Raw264.7 cells using anti-Androgen receptor/AR antibody (A00542).
  Overlay histogram showing Raw264.7 cells stained with A00542 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Androgen receptor/AR Antibody (A00542) at 1:100 dilution for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG at 1:100 dilution used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.

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  IF analysis of Androgen receptor/AR using anti-Androgen receptor/AR antibody (A00542).
  Androgen receptor/AR was detected in an immunocytochemical section of T-47D cells. The section was incubated with rabbit anti-Androgen receptor/AR Antibody (A00542) at a dilution of 1:100. DyLight®488 Conjugated Goat Anti-Rabbit IgG (Green) (Catalog # BA1127) was used as secondary antibody. The section was counterstained with DAPI (Catalog # AR1176) (Blue).

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  Western blot analysis of Androgen receptor/AR using anti-Androgen receptor/AR antibody (A00542). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
  Lane 1: Human K562 whole cell lysates,
  Lane 2: Human U2OS whole cell lysates,
  Lane 3: Human HEK293 whole cell lysates,
  Lane 4: Human PC-3 whole cell lysates,
  Lane 5: Human 22RV1 whole cell lysates,
  Lane 6: Human HepG2 whole cell lysates,
  Lane 7: Human CACO-2 whole cell lysates.
  After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-Androgen receptor/AR antigen affinity purified polyclonal antibody (A00542) at a dilution of 1:1000 and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for Androgen receptor/AR at approximately 110-120 kDa. The expected band size for Androgen receptor/AR is at 99 kDa.

• 

  Flow Cytometry analysis of A549 cells using anti-Androgen receptor/AR antibody (A00542).
  Overlay histogram showing A549 cells stained with A00542 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Androgen receptor/AR Antibody (A00542) at 1:100 dilution for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG at 1:100 dilution used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.

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  Flow Cytometry analysis of C6 cells using anti-Androgen receptor/AR antibody (A00542).
  Overlay histogram showing C6 cells stained with A00542 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Androgen receptor/AR Antibody (A00542) at 1:100 dilution for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG at 1:100 dilution used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.

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  Flow Cytometry analysis of Raw264.7 cells using anti-Androgen receptor/AR antibody (A00542).
  Overlay histogram showing Raw264.7 cells stained with A00542 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Androgen receptor/AR Antibody (A00542) at 1:100 dilution for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG at 1:100 dilution used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.

• 

  IF analysis of Androgen receptor/AR using anti-Androgen receptor/AR antibody (A00542).
  Androgen receptor/AR was detected in an immunocytochemical section of T-47D cells. The section was incubated with rabbit anti-Androgen receptor/AR Antibody (A00542) at a dilution of 1:100. DyLight®488 Conjugated Goat Anti-Rabbit IgG (Green) (Catalog # BA1127) was used as secondary antibody. The section was counterstained with DAPI (Catalog # AR1176) (Blue).

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