Anti-BDNF antibody [EPR1292] - BSA and Azide free

11 product images

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  Western blot - Anti-BDNF antibody [EPR1292] - BSA and Azide free (ab271873)

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-BDNF antibody [EPR1292] ab108319).

  This blot was produced using a 4-12% Bis-tris gel under the MES buffer system. The gel was run at 200V for 35 minutes before being transferred onto a Nitrocellulose membrane at 30V for 70 minutes. The membrane was then blocked for an hour using Licor blocking buffer before being incubated with unpurified Anti-BDNF antibody [EPR1292] ab108319 (1/1000) overnight at 4°C. Anti-GAPDH antibody [6C5] - Loading Control ab8245 (mouse anti-GAPDH; 0.05 ug/mL) was included as a loading control. Antibody binding was detected using goat anti-rabbit IgG IR-680 (green) and goat anti-mouse IgG IR800 (red) at a 1:10,000 dilution for 1hr at room temperature and then imaged using the Licor Odyssey CLx

  All lanes: Western blot - Anti-BDNF antibody [EPR1292] (Anti-BDNF antibody [EPR1292] ab108319) at 1/1000 dilution

  Lane 1: Human hippocampus lysate at 20 µg

  Lane 2: Rat hippocampus lysate at 20 µg

  Lane 3: Mouse hippocampus lysate at 20 µg

  Secondary

  All lanes: Gt anti Rb IR680 at 1/10000 dilution

  Performed under reducing conditions.

  Predicted band size: 27 kDa

  Observed band size: 15 kDa, 28 kDa, 35 kDa, 45 kDa

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-BDNF antibody [EPR1292] - BSA and Azide free (ab271873)

  This data was developed using the same antibody clone in a different buffer formulation (Anti-BDNF antibody [EPR1292] ab108319).
  

  IHC image of BDNF staining in a section of frozen normal human cerebral cortex performed on a Leica BOND^TM system using the standard protocol. The section was fixed in 10% paraformaldehyde (10 min) prior to staining. The section was incubated with Anti-BDNF antibody [EPR1292] ab108319, 1/200 dilution, for 15 mins at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX. The inset secondary-only control image is taken from an identical assay without primary antibody.

  For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.

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  Western blot - Anti-BDNF antibody [EPR1292] - BSA and Azide free (ab271873)

  This data was developed using Anti-BDNF antibody [EPR1292] ab108319, the same antibody clone in a different buffer formulation.

  All lanes: Western blot - Anti-BDNF antibody [EPR1292] (Anti-BDNF antibody [EPR1292] ab108319) at 1/1000 dilution

  Lane 1: Human brain lysates at 20 µg

  Lane 2: Mouse brain lysates at 20 µg

  Lane 3: Rat brain lysates at 20 µg

  Lane 4: Human hippocampus lysates at 20 µg

  Lane 5: Mouse hippocampus lysates at 20 µg

  Lane 6: Rat hippocampus lysates at 20 µg

  Lane 7: Human cerebellum lysates at 20 µg

  Lane 8: Mouse cerebellum lysates at 20 µg

  Lane 9: Rat cerebellum lysates at 20 µg

  Secondary

  All lanes: Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity with human IgG at 1/2000 dilution

  Predicted band size: 27 kDa

  Observed band size: 15-45 kDa

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  Immunohistochemistry (Frozen sections) - Anti-BDNF antibody [EPR1292] - BSA and Azide free (ab271873)

  Immunohistochemistry (Frozen sections) analysis of rat cerebral cortex tissue sections labeling BDNF with Purified Anti-BDNF antibody [EPR1292] ab108319 at 1/100 (2.8 μg/ml).Heat mediated antigen retrieval using sodium citrate buffer (10mM citrate pH 6.0 + 0.05% Tween-20). Goat anti rabbit IgG (Alexa Fluor® 488, Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077) was used as the secondary antibody. Negative control: PBS instead of the primary antibody. DAPI was used as a counterstain.
  

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-BDNF antibody [EPR1292] ab108319).

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-BDNF antibody [EPR1292] - BSA and Azide free (ab271873)

  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of Human bladder cancer tissue sections labeling BDNF with Purified Anti-BDNF antibody [EPR1292] ab108319 at 1:500 dilution (0.56 µg/ml). Heat mediated antigen retrieval was performed using Antigen Retrieval Buffer (100X Tris-EDTA Buffer, pH 9.0) ab93684 (Tris/EDTA buffer, pH 9.0)This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-BDNF antibody [EPR1292] ab108319).

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  Flow Cytometry (Intracellular) - Anti-BDNF antibody [EPR1292] - BSA and Azide free (ab271873)

  Intracellular Flow Cytometry analysis of HeLa (Human cervix adenocarcinoma epithelial cell) cells labeling BDNF with purified Anti-BDNF antibody [EPR1292] ab108319 at 1/30 dilution (10 μg/ml) (red). Cells were fixed with 80% methanol. A Goat anti rabbit IgG (Alexa Fluor^® 488) secondary antibody was used at 1/2000 dilution. Isotype control - Rabbit monoclonal IgG (Black). Unlabeled control - Cell without incubation with primary antibody and secondary antibody (Blue).
  

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-BDNF antibody [EPR1292] ab108319).

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  Western blot - Anti-BDNF antibody [EPR1292] - BSA and Azide free (ab271873)

  This data was developed using Anti-BDNF antibody [EPR1292] ab108319, the same antibody clone in a different buffer formulation. Different batches of Anti-BDNF antibody [EPR1292] ab108319 were tested on Mouse brain lysate at 0.3 µg/ml. 15 µg of lysate was loaded in each lane. Bands observed at 14-45 kDa.

  All lanes: Western blot - Anti-BDNF antibody [EPR1292] (Anti-BDNF antibody [EPR1292] ab108319)

  Predicted band size: 27 kDa

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  Immunohistochemistry (Frozen sections) - Anti-BDNF antibody [EPR1292] - BSA and Azide free (ab271873)

  Immunohistochemistry (Frozen sections) analysis of mouse cerebrum tissue sections labeling BDNF with Purified Anti-BDNF antibody [EPR1292] ab108319 at 1/100 (2.8 μg/ml).Heat mediated antigen retrieval using sodium citrate buffer (10mM citrate pH 6.0 + 0.05% Tween-20). Goat anti rabbit IgG (Alexa Fluor® 488, Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077) was used as the secondary antibody. Negative control: PBS instead of the primary antibody. DAPI was used as a counterstain.
  

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-BDNF antibody [EPR1292] ab108319).

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  Immunocytochemistry/ Immunofluorescence - Anti-BDNF antibody [EPR1292] - BSA and Azide free (ab271873)

  Immunocytochemistry/ Immunofluorescence analysis of HeLa (Human cervix adenocarcinoma epithelial cell) cells labeling BDNF with Purified Anti-BDNF antibody [EPR1292] ab108319 at 1:500 (0.6 µg/ml). Cells were fixed in 100% Methanol and permeabilized with None. Cells were counterstained with Alexa Fluor® 594 Anti-alpha Tubulin antibody [DM1A] - Microtubule Marker ab195889 Anti-alpha Tubulin antibody [DM1A] - Microtubule Marker (Alexa Fluor^® 594) 1:200 (2.5 µg/ml). Goat anti rabbit IgG (Alexa Fluor^® 488, Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077) was used as the secondary antibody at 1:1000 (2 µg/ml) dilution. DAPI nuclear counterstain. PBS instead of the primary antibody was used as the secondary antibody only control.This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-BDNF antibody [EPR1292] ab108319).

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-BDNF antibody [EPR1292] - BSA and Azide free (ab271873)

  Immunohistochemical analysis of paraffin-embedded human brain tissue using unpurified Anti-BDNF antibody [EPR1292] ab108319 at 1/100 dilution.

  Perform heat mediated antigen retrieval before commencing with IHC staining protocol.

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-BDNF antibody [EPR1292] ab108319).

• 

  Western blot - Anti-BDNF antibody [EPR1292] - BSA and Azide free (ab271873)

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-BDNF antibody [EPR1292] ab108319).

  Blocking and diluting buffer and concentration: 5% NFDM/TBST

  Anti-6X His tag® antibody [EPR20547] - ChIP Grade ab213204 was used as a His tag loading control.

  All lanes: Western blot - Anti-BDNF antibody [EPR1292] (Anti-BDNF antibody [EPR1292] ab108319) at 1/1000 dilution

  Lane 1: 293T cells transfected with an empty vector containing a His tag whole cell lysate at 20 µg

  Lane 2: 293T cells transfected with a Human BDNF expression vector containing a His-tag whole cell lysate at 20 µg

  Lane 3: 293T cells transfected with a Human NGF expression vector containing a His-tag whole cell lysate at 20 µg

  Lane 4: 293T cells transfected with a Human NTF3 expression vector containing a His-tag whole cell lysate at 20 µg

  Lane 5: 293T cells transfected with a Human NTF4 expression vector containing a His-tag whole cell lysate at 20 µg

  Secondary

  All lanes: Western blot - Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/20000 dilution

  Observed band size: 35 kDa

  Exposure time: 1s