Anti-TPPP antibody [EPR3316] - BSA and Azide free

9 product images

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  Immunocytochemistry/ Immunofluorescence - Anti-TPPP antibody [EPR3316] - BSA and Azide free (ab238958)

  Immunocytochemistry/Immunofluorescence staining of Neuro-2a (mouse neuroblastoma) cells labelling TPPP with purified Anti-TPPP antibody [EPR3316] ab92305 at a working dilution of 1/100. The secondary antibody was Alexa Fluor® 488 goat anti-rabbit (Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077), used at a dilution of 1/1000. Anti-alpha Tubulin antibody [DM1A] - Loading Control ab7291, a mouse anti-tubulin antibody (1/1000), was used to stain tubulin along with Goat Anti-Mouse IgG H&L (Alexa Fluor® 594) preadsorbed ab150120 (Alexa Fluor® 594 goat anti-mouse, 1/1000), shown in the top right hand panel. DAPI was used as nuclear counterstain. The cells were fixed in 4% Paraformaldehyde and permeabilized using 0.1% Triton X-100. The negative controls are shown in bottom middle and right hand panels - for negative control 1, rabbit primary antibody was used followed by an Alexa Fluor® 594 goat anti-mouse antibody (Goat Anti-Mouse IgG H&L (Alexa Fluor® 594) preadsorbed ab150120). For negative control 2, Anti-alpha Tubulin antibody [DM1A] - Loading Control ab7291 (mouse anti-tubulin) was used followed by an Alexa Fluor® 488 goat anti-rabbit secondary (Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077).

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-TPPP antibody [EPR3316] ab92305).

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-TPPP antibody [EPR3316] - BSA and Azide free (ab238958)

  Immunohistochemical analysis of paraffin-embedded rat cerebral cortex tissue sections labelling TPPP with purified Anti-TPPP antibody [EPR3316] ab92305 at dilution of 1/50. The secondary antibody used was Goat Anti-Rabbit IgG H&L (HRP) ab97051; a goat anti-rabbit IgG H&L (HRP) at dilution of 1/500. The sample was counterstained with hematoxylin. Antigen retrieval was performed using EDTA Buffer; pH 9.0. PBS was used instead of the primary antibody as the negative control and is shown in the inset.

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-TPPP antibody [EPR3316] ab92305).

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-TPPP antibody [EPR3316] - BSA and Azide free (ab238958)

  Immunohistochemical analysis of paraffin-embedded mouse cerebral cortex tissue sections labelling TPPP with purified Anti-TPPP antibody [EPR3316] ab92305 at dilution of 1/50. The secondary antibody used was Goat Anti-Rabbit IgG H&L (HRP) ab97051; a goat anti-rabbit IgG H&L (HRP) at dilution of 1/500. The sample was counterstained with hematoxylin. Antigen retrieval was performed using EDTA Buffer; pH 9.0. PBS was used instead of the primary antibody as the negative control and is shown in the inset.

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-TPPP antibody [EPR3316] ab92305).

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-TPPP antibody [EPR3316] - BSA and Azide free (ab238958)

  Immunohistochemical analysis of paraffin-embedded human glioma tissue sections labelling TPPP with purified Anti-TPPP antibody [EPR3316] ab92305 at dilution of 1/50. The secondary antibody used was Goat Anti-Rabbit IgG H&L (HRP) ab97051; a goat anti-rabbit IgG H&L (HRP) at dilution of 1/500. The sample was counterstained with hematoxylin. Antigen retrieval was performed using EDTA Buffer; pH 9.0. PBS was used instead of the primary antibody as the negative control and is shown in the inset.

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-TPPP antibody [EPR3316] ab92305).

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  Flow Cytometry (Intracellular) - Anti-TPPP antibody [EPR3316] - BSA and Azide free (ab238958)

  Overlay histogram showing SH-SY5Y cells stained with Anti-TPPP antibody [EPR3316] ab92305 (red line). The cells were fixed with 4% paraformaldehyde (10 min) and then permeabilized with 0.1% PBS-Tween for 20 min. The cells were then incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions followed by the antibody (Anti-TPPP antibody [EPR3316] ab92305, 1/100 dilution) for 30 min at 22°C. The secondary antibody used was DyLight® 488 goat anti-rabbit IgG (H+L) (Goat Anti-Rabbit IgG H&L (DyLight® 488) preadsorbed ab96899) at 1/500 dilution for 30 min at 22°C. Isotype control antibody (black line) was rabbit IgG (monoclonal) (0.1μg/1x10⁶ cells) used under the same conditions. Unlabelled sample (blue line) was also used as a control. Acquisition of >5,000 events were collected using a 20mW Argon ion laser (488nm) and 525/30 bandpass filter. This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-TPPP antibody [EPR3316] ab92305).
  

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-TPPP antibody [EPR3316] - BSA and Azide free (ab238958)

  Anti-TPPP antibody [EPR3316] ab92305 at 1/250 dilution staining TPPP in paraffin-embedded Human brain tissue by immunohistochemistry.
  

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-TPPP antibody [EPR3316] ab92305).

  Perform heat mediated antigen retrieval via the pressure cooker method before commencing with IHC staining protocol.

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  Immunocytochemistry/ Immunofluorescence - Anti-TPPP antibody [EPR3316] - BSA and Azide free (ab238958)

  Anti-TPPP antibody [EPR3316] ab92305 at 1/100 dilution staining TPPP in SH-SY5Y cells, by immunofluorescence.

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-TPPP antibody [EPR3316] ab92305).

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-TPPP antibody [EPR3316] - BSA and Azide free (ab238958)

  Immunohistochemical analysis of paraffin-embedded human cerebral cortex tissue sections labelling TPPP with purified Anti-TPPP antibody [EPR3316] ab92305 at dilution of 1/50. The secondary antibody used was Goat Anti-Rabbit IgG H&L (HRP) ab97051; a goat anti-rabbit IgG H&L (HRP) at dilution of 1/500. The sample was counterstained with hematoxylin. Antigen retrieval was performed using EDTA Buffer; pH 9.0. PBS was used instead of the primary antibody as the negative control and is shown in the inset.
  

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-TPPP antibody [EPR3316] ab92305).

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  Flow Cytometry (Intracellular) - Anti-TPPP antibody [EPR3316] - BSA and Azide free (ab238958)

  Overlay histogram showing 4% paraformaldehyde fixed Neuro-2a (mouse neuroblastoma) cells labelling TPPP with purified Anti-TPPP antibody [EPR3316] ab92305 at dilution of 1/20. The secondary antibody used was Alexa Fluor^® 488 goat-anti-rabbit IgG at dilution of 1/2000. A non-specific IgG antibody (rabbit monoclonal) was used as isotype control (black line). The blue line shows cells without incubation with primary antibody and secondary antibody.
  

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-TPPP antibody [EPR3316] ab92305).