Anti-HSPH1 Antibody

筛选器： All WB IHC ICC/IF FCM

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  Figure 1. Western blot analysis of HSPH1 using anti-HSPH1 antibody (BA0931). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
  Lane 1: rat ovary Tissue lysates,
  Lane 2: human A549 whole cell lysates,
  Lane 3: human U87 whole cell lysates,
  Lane 4: human Hela whole cell lysates.
  After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-HSPH1 antigen affinity purified polyclonal antibody (BA0931) 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 HSPH1 at approximately 105 kDa. The expected band size for HSPH1 is at 97 kDa.

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  Figure 2. IHC analysis of HSPH1 using anti-HSPH1 antibody (BA0931).
  HSPH1 was detected in a paraffin-embedded section of human mammary cancer tissue. The tissue section was incubated with rabbit anti-HSPH1 Antibody (BA0931) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.

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  Figure 3. IF analysis of HSPH1 using anti-HSPH1 antibody (BA0931).
  HSPH1 was detected in an immunocytochemical section of A549 cells. The section was incubated with rabbit anti-HSPH1 Antibody (BA0931) 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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  Figure 4. Flow Cytometry analysis of A431 cells using anti-HSPH1 antibody (BA0931).
  Overlay histogram showing A431 cells stained with BA0931 (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-HSPH1 Antibody (BA0931) 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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  Figure 1. Western blot analysis of HSPH1 using anti-HSPH1 antibody (BA0931). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
  Lane 1: rat ovary Tissue lysates,
  Lane 2: human A549 whole cell lysates,
  Lane 3: human U87 whole cell lysates,
  Lane 4: human Hela whole cell lysates.
  After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-HSPH1 antigen affinity purified polyclonal antibody (BA0931) 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 HSPH1 at approximately 105 kDa. The expected band size for HSPH1 is at 97 kDa.

• 

  Figure 2. IHC analysis of HSPH1 using anti-HSPH1 antibody (BA0931).
  HSPH1 was detected in a paraffin-embedded section of human mammary cancer tissue. The tissue section was incubated with rabbit anti-HSPH1 Antibody (BA0931) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.

• 

  Figure 3. IF analysis of HSPH1 using anti-HSPH1 antibody (BA0931).
  HSPH1 was detected in an immunocytochemical section of A549 cells. The section was incubated with rabbit anti-HSPH1 Antibody (BA0931) 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).

• 

  Figure 4. Flow Cytometry analysis of A431 cells using anti-HSPH1 antibody (BA0931).
  Overlay histogram showing A431 cells stained with BA0931 (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-HSPH1 Antibody (BA0931) 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.