Anti-SOX18 Antibody

筛选器： All WB ICC/IF FCM ELISA

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  Western blot analysis of SOX18 using anti-SOX18 antibody (A04004-2). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
  Lane 1: human Jurkat whole cell lysates,
  Lane 2: human COLO-320 whole cell lysates,
  Lane 3: human HELA whole cell lysates,
  Lane 4: human HEPG2 whole cell lysates,
  Lane 5: Monkey COS-7 whole cell lysates,
  Lane 6: rat heart tissue lysates,
  Lane 7: rat lung tissue lysates,
  Lane 8: rat liver tissue lysates,
  Lane 9: mouse lung tissue lysates,
  Lane 10: mouse liver tissue lysates.
  After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-SOX18 antigen affinity purified polyclonal antibody (A04004-2) 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 SOX18 at approximately 41 kDa. The expected band size for SOX18 is at 41 kDa.

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  IF analysis of SOX18 using anti-SOX18 antibody (A04004-2).
  SOX18 was detected in an immunocytochemical section of HepG2 cells. The section was incubated with rabbit anti-SOX18 Antibody (A04004-2) 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 HepG2 cells using anti-SOX18 antibody (A04004-2).
  Overlay histogram showing HepG2 cells stained with A04004-2 (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-SOX18 Antibody (A04004-2) 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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  Western blot analysis of SOX18 using anti-SOX18 antibody (A04004-2). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
  Lane 1: human Jurkat whole cell lysates,
  Lane 2: human COLO-320 whole cell lysates,
  Lane 3: human HELA whole cell lysates,
  Lane 4: human HEPG2 whole cell lysates,
  Lane 5: Monkey COS-7 whole cell lysates,
  Lane 6: rat heart tissue lysates,
  Lane 7: rat lung tissue lysates,
  Lane 8: rat liver tissue lysates,
  Lane 9: mouse lung tissue lysates,
  Lane 10: mouse liver tissue lysates.
  After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-SOX18 antigen affinity purified polyclonal antibody (A04004-2) 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 SOX18 at approximately 41 kDa. The expected band size for SOX18 is at 41 kDa.

• 

  IF analysis of SOX18 using anti-SOX18 antibody (A04004-2).
  SOX18 was detected in an immunocytochemical section of HepG2 cells. The section was incubated with rabbit anti-SOX18 Antibody (A04004-2) 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).

• 

  Flow Cytometry analysis of HepG2 cells using anti-SOX18 antibody (A04004-2).
  Overlay histogram showing HepG2 cells stained with A04004-2 (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-SOX18 Antibody (A04004-2) 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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