Anti-ASIC2 Antibody

筛选器： All WB ICC/IF FCM ELISA

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  Western blot analysis of ASIC2 using anti-ASIC2 antibody (A04055-1). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
  Lane 1: human placenta tissue lysates,
  Lane 2: human PC-3 whole cell lysates,
  Lane 3: human A549 whole cell lysates,
  Lane 4: human U2OS whole cell lysates,
  Lane 5: rat brain tissue lysates,
  Lane 6: rat liver tissue lysates,
  Lane 7: rat ovarian tissue lysates,
  Lane 8: mouse brain tissue lysates,
  Lane 9: mouse liver tissue lysates,
  Lane 10: mouse ovarian tissue lysates.
  After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-ASIC2 antigen affinity purified polyclonal antibody (A04055-1) 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 ASIC2 at approximately 58 kDa. The expected band size for ASIC2 is at 58 kDa.

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  IF analysis of ASIC2 using anti-ASIC2 antibody (A04055-1).
  ASIC2 was detected in an immunocytochemical section of A431 cells. The section was incubated with rabbit anti-ASIC2 Antibody (A04055-1) 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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  Flow Cytometry analysis of A549 cells using anti-ASIC2 antibody (A04055-1).
  Overlay histogram showing A549 cells stained with A04055-1 (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-ASIC2 Antibody (A04055-1) 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 PC-3 cells using anti-ASIC2 antibody (A04055-1).
  Overlay histogram showing PC-3 cells stained with A04055-1 (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-ASIC2 Antibody (A04055-1) 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.

• 

  Western blot analysis of ASIC2 using anti-ASIC2 antibody (A04055-1). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
  Lane 1: human placenta tissue lysates,
  Lane 2: human PC-3 whole cell lysates,
  Lane 3: human A549 whole cell lysates,
  Lane 4: human U2OS whole cell lysates,
  Lane 5: rat brain tissue lysates,
  Lane 6: rat liver tissue lysates,
  Lane 7: rat ovarian tissue lysates,
  Lane 8: mouse brain tissue lysates,
  Lane 9: mouse liver tissue lysates,
  Lane 10: mouse ovarian tissue lysates.
  After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-ASIC2 antigen affinity purified polyclonal antibody (A04055-1) 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 ASIC2 at approximately 58 kDa. The expected band size for ASIC2 is at 58 kDa.

• 

  IF analysis of ASIC2 using anti-ASIC2 antibody (A04055-1).
  ASIC2 was detected in an immunocytochemical section of A431 cells. The section was incubated with rabbit anti-ASIC2 Antibody (A04055-1) 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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  Flow Cytometry analysis of A549 cells using anti-ASIC2 antibody (A04055-1).
  Overlay histogram showing A549 cells stained with A04055-1 (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-ASIC2 Antibody (A04055-1) 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.

• 

  Flow Cytometry analysis of PC-3 cells using anti-ASIC2 antibody (A04055-1).
  Overlay histogram showing PC-3 cells stained with A04055-1 (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-ASIC2 Antibody (A04055-1) 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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