Anti-TRIM36 Antibody

筛选器： All WB ICC/IF FCM ELISA

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  Western blot analysis of TRIM36 using anti-TRIM36 antibody (A10270-3). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
  Lane 1: rat testis tissue lysates,
  Lane 2: mouse testis tissue lysates.
  After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-TRIM36 antigen affinity purified polyclonal antibody (A10270-3) 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 TRIM36 at approximately 83 kDa. The expected band size for TRIM36 is at 83 kDa.

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  IF analysis of TRIM36 using anti-TRIM36 antibody (A10270-3) and anti-Alpha Tubulin antibody (M03989-3).
  TRIM36 was detected in an immunocytochemical section of U2OS cells. The section was incubated with rabbit anti-TRIM36 Antibody (A10270-3) at a dilution of 1:100. Cy3-conjugated Anti-rabbit IgG Secondary Antibody (red)(Catalog#BA1032) and Dylight488-conjugated Anti-mouse IgG Secondary Antibody (Green) (Catalog # BA1126) were used as secondary antibody.

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  Flow Cytometry analysis of Hela cells using anti-TRIM36 antibody (A10270-3).
  Overlay histogram showing Hela cells stained with A10270-3 (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-TRIM36 Antibody (A10270-3) 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 TRIM36 using anti-TRIM36 antibody (A10270-3). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
  Lane 1: rat testis tissue lysates,
  Lane 2: mouse testis tissue lysates.
  After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-TRIM36 antigen affinity purified polyclonal antibody (A10270-3) 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 TRIM36 at approximately 83 kDa. The expected band size for TRIM36 is at 83 kDa.

• 

  IF analysis of TRIM36 using anti-TRIM36 antibody (A10270-3) and anti-Alpha Tubulin antibody (M03989-3).
  TRIM36 was detected in an immunocytochemical section of U2OS cells. The section was incubated with rabbit anti-TRIM36 Antibody (A10270-3) at a dilution of 1:100. Cy3-conjugated Anti-rabbit IgG Secondary Antibody (red)(Catalog#BA1032) and Dylight488-conjugated Anti-mouse IgG Secondary Antibody (Green) (Catalog # BA1126) were used as secondary antibody.

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  Flow Cytometry analysis of Hela cells using anti-TRIM36 antibody (A10270-3).
  Overlay histogram showing Hela cells stained with A10270-3 (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-TRIM36 Antibody (A10270-3) 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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