Anti-Doublecortin antibody

17 product images

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  Immunohistochemistry (PFA perfusion fixed frozen sections) - Anti-Doublecortin antibody (ab18723)

  IHC image of Doublecortin staining in a section of frozen PFA perfusion fixed 6 week old rat dentate gyrus. After dissection, the tissue was further fixed in PFA overnight, washed in PBS and then incubated overnight in 30% sucrose. It was then embedded in OCT and cryosectioned. Non-specific protein-protein interactions were blocked in TBS containing 0.025% (v/v) Triton X-100, 0.3M glycine and 1% (w/v) BSA for 1h at room temperature. The section was incubated overnight at +4°C in TBS containing 0.025% (v/v) Triton X-100 and 1% (w/v) BSA with ab18723 at 1/1300 dilution and then incubated with Goat Anti-Rabbit IgG H&L (Alexa Fluor® 594) ab150080 (Goat Anti-Rabbit IgG H&L (Alexa Fluor^® 594) preabsorbed, (Shown in red) 1/1000) for 1 hour at room temperature. DAPI was used to stain the cell nuclei (blue). The secondary-only control insert image is taken from an identical assay without primary antibody.
  Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
  For IHC staining systems (automated and non-automated), customers should optimize variable parameters such as antibody concentrations and incubation times.

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  Immunohistochemistry (PFA perfusion fixed frozen sections) - Anti-Doublecortin antibody (ab18723)

  IHC image of Doublecortin staining in a section of frozen PFA perfusion fixed 8 week old mouse SVZ. After dissection, the tissue was further fixed in PFA overnight, washed in PBS and then incubated overnight in 30% sucrose. It was then embedded in OCT and cryosectioned. Non-specific protein-protein interactions were blocked in TBS containing 0.025% (v/v) Triton X-100, 0.3M glycine and 1% (w/v) BSA for 1h at room temperature. The section was incubated overnight at +4°C in TBS containing 0.025% (v/v) Triton X-100 and 1% (w/v) BSA with ab18723 at 1/2000 dilution and then incubated with Goat Anti-Rabbit IgG H&L (Alexa Fluor® 594) ab150080 (Goat Anti-Rabbit IgG H&L (Alexa Fluor^® 594) preabsorbed, (Shown in red) 1/1000) for 1 hour at room temperature. DAPI was used to stain the cell nuclei (blue). The secondary-only control insert image is taken from an identical assay without primary antibody.
  Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
  For IHC staining systems (automated and non-automated), customers should optimize variable parameters such as antibody concentrations and incubation times.

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  Immunohistochemistry (PFA perfusion fixed frozen sections) - Anti-Doublecortin antibody (ab18723)

  IHC image of Doublecortin staining in a section of frozen PFA perfusion fixed 8 week old mouse dentate gyrus. After dissection, the tissue was further fixed in PFA overnight, washed in PBS and then incubated overnight in 30% sucrose. It was then embedded in OCT and cryosectioned. Non-specific protein-protein interactions were blocked in TBS containing 0.025% (v/v) Triton X-100, 0.3M glycine and 1% (w/v) BSA for 1h at room temperature. The section was incubated overnight at +4°C in TBS containing 0.025% (v/v) Triton X-100 and 1% (w/v) BSA with ab18723 at 1/2000 dilution and then incubated with Goat Anti-Rabbit IgG H&L (Alexa Fluor® 594) ab150080 (Goat Anti-Rabbit IgG H&L (Alexa Fluor^® 594) preabsorbed, (Shown in red) 1/1000) for 1 hour at room temperature. DAPI was used to stain the cell nuclei (blue). The secondary-only control insert image is taken from an identical assay without primary antibody.
  Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
  For IHC staining systems (automated and non-automated), customers should optimize variable parameters such as antibody concentrations and incubation times.

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  Western blot - Anti-Doublecortin antibody (ab18723)

  Blocking buffer: 3% Milk
  

  Gel type: MOPS

  Exposure Time: 1 minute 30 seconds

  All lanes: Western blot - Anti-Doublecortin antibody (ab18723) at 1 µg/mL

  Lane 1: Mouse brain tissue lysate - total protein (0 days) at 10 µg

  Lane 2: Rat brain tissue lysate - total protein (0 days) at 10 µg

  Secondary

  All lanes: Goat polyclonal to Rabbit IgG - H&L - Pre-Adsorbed (HRP) at 1/50000 dilution

  Predicted band size: 49 kDa

  Observed band size: 45 kDa

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  This image is courtesy of an anonymous customer review.

  Immunohistochemistry (PFA perfusion fixed frozen sections) - Anti-Doublecortin antibody (ab18723)

  IHC-FoFr image of Doublecortin staining in Mouse adult dentate gyrus sections using ab18723 (1/100 dilution). The sections were fixed in paraformaldehyde and permeabilized using 1x TBST. The sections were then blocked using 10% donkey serum for 1 hour at 25°C. ab18723 was diluted 1/100 and incubated with the sections for 12 hours at 25°C. The secondary antibody used was Donkey anti-rabbit conjugated to Cy3 Dye (1/500 dilution). DAPI was used to stain the nuclei.

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Doublecortin antibody (ab18723)

  Doublecortin Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) staining of mouse brain using rabbit Anti-Doublecortin antibody

  IHC image of ab18723 staining in Mouse 8 weeks brain formalin fixed paraffin embedded tissue section, performed on a Leica BOND^TM system using the standard protocol F (with no post primary). The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH6, epitope retrieval solution 1) for 20 mins. The section was then incubated with ab18723, 0.1μg/ml, 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. Secondary-only control image is shown as insert.
  

  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-Doublecortin antibody (ab18723)

  All lanes: Western blot - Anti-Doublecortin antibody (ab18723) at 1 µg/mL

  All lanes: Western blot - Mouse brain tissue lysate - total protein (0 days) (Mouse brain tissue lysate - total protein (0 days) ab7188) at 10 µg

  Secondary

  All lanes: Goat polyclonal to Rabbit IgG - H&L - Pre-Adsorbed (HRP) at 1/3000 dilution

  Performed under reducing conditions.

  Predicted band size: 49 kDa

  Observed band size: 45 kDa, 49 kDa

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Doublecortin antibody (ab18723)

  Doublecortin Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) staining of rat brain tissue using rabbit Anti-Doublecortin antibody

  IHC image of ab18723 staining in rat 6 week brain formalin fixed paraffin embedded tissue section performed on a Leica Bond^TM system using the standard protocol F. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH6) for 20 mins. The section was then incubated with ab18723 0.1μg/ml 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.
  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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  This image is courtesy of Francois Guillemot, NIMR, UK

  Immunohistochemistry (PFA perfusion fixed frozen sections) - Anti-Doublecortin antibody (ab18723)

  Doublecortin Immunohistochemistry (PFA perfusion fixed frozen sections) staining of mouse brain using rabbit Anti-Doublecortin antibody

  Doublecortin expression in the dentate gyrus of a 1 month-old mouse brain. Doublecortin staining using ab18723 (1/500 dilution) in the dentate gyrus of a 1 month-old mouse brain. The mouse has been perfused with paraformaldehyde 4% (50ml). After dissection the brain has been incubated overnight in sucrose 20% embedded in OCT and cryosectioned (10 µm). No antigen retrieval was used. The secondary antibody used was a non-Abcam Goat anti-rabbit Alexa488.

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Doublecortin antibody (ab18723)

  Doublecortin Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) staining of rat brain tissue using rabbit Anti-Doublecortin antibody

  ab18723 staining 6 week rat brain tissue dentate gyrus (DG) by IHC-P using rabbit-specific EXPOSE IHC detection kit (ab80437). Formalin fixed paraffin embedded tissue sections were pre-treated using heat mediated antigen retrieval (using a pressure cooker) with sodium citrate buffer (pH6) for 30 mins. The section was incubated with ab18723 0.1μg/ml for 1 hour at room temperature. DAB was used as the chromogen and the section was counterstained with haematoxylin and mounted with DPX.

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  This image is courtesy of Carl Hobbs, King's College London, United Kingdom

  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Doublecortin antibody (ab18723)

  ab18723 at 1/200 staining mouse E18 body T/S spinal cord tissue sections by IHC-P. The tissue was formaldehyde fixed and a heat mediated antigen retireval step was perfomed before incubation with the antibody for 24 hours. A biotinylated goat antibody was used as the secondary.

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  This image is courtesy of Randal Moldrich, CNRS UMR7637, ESPCI, France

  Immunocytochemistry/ Immunofluorescence - Anti-Doublecortin antibody (ab18723)

  Doublecortin antibody (ab18723; green) labeling cell extensions from rat embryos consistent with dendrite morphology in 4 day old cultures. Preincubation of ab18723 with its immunising peptide (Human Doublecortin peptide ab19804) quenched immunostaining (see review).
  

  Dorsal root ganglion explants were dissected from 16 day-old rat embryos and cultured for 4 days in vitro with Neurobasal Medium containing 10% fetal calf serum and B27 supplement. Immunocytochemistry: All steps were performed in PBS. Cells or explants were fixed in 4% PFA for 15min, permeabilised with 0.1% TX100 for 10min and blocked with 5% BSA, 0.1% TX100 for 45min. ab18723 was incubated at 5μg/ml for 12h in 5% BSA, 0.1% TX100 at 4°C. For peptide blocking experiments preincubation of the peptide (Human Doublecortin peptide ab19804; 250μg/ml) and antibody (5μg/ml ) was performed for 2h at 37°C. Cultures were washed (3x) of primary antibody solution. Goat anti-rabbit AlexaFluor 488 was used as secondary antibody (1/400) in 5% BSA, 0.1% TX100 for 2h at R

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  This image is courtesy of Carl Hobbs, King's College London, United Kingdom

  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Doublecortin antibody (ab18723)

  Immunohistochemistical staining (on formaldehyde/PFA-fixed paraffin-embedded sections) of Doublecortin antibody - Neuronal Marker (ab18723) on Quail Tissue sections (E6/7 brain (Saggital section). Antigen retrieval step: Heat mediated. Blocking step: 1% BSA for 10 mins at RT. Primary Antibody ab18723 incubated at 1/400 for 2 hours RT. Secondary Antibody: Biotin conjugated goat anti rabbit Ig
  (1/300).

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  This image is courtesy of Carl Hobbs, King's College London, United Kingdom

  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Doublecortin antibody (ab18723)

  ab18723 at 1/2000 staining mouse brain svr: progenitor olfactory neurones by IHC-P. The tissue was formaldehyde fixed and a heat mediated antigen retrieval step was performed before incubation with the antibody for 16 hours. An Alexa-Fluor ® 488 conjugated goat antibody was used as the secondary (green). The tissue was also stained for Ki67 (shown in red).

  The MIP image was derived from Apotome-generated Z-stacks from the greyscale image of each of the channels in the MIP.

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Doublecortin antibody (ab18723)

  Immunohistochemical analysis of formalin-fixed paraffin-embedded mouse brain labelling doublecortin with ab18723 at a dilution of 0.8µg/ml. The immunostaining was performed on a Ventana DISCOVERY ULTRA (Roche Tissue Diagnostics) instrument with an OptiView DAB IHC Detection Kit. Heat mediated antigen retrieval was conducted for 32min with ULTRA cell conditioning solution (CC1 pH8.5). ab18723 anti doublecortin antibody was incubated at 37°C for 16min. Sections were counterstained is with Hematoxylin II. Image inset shows absence of staining in secondary antibody only control.

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  Immunocytochemistry/ Immunofluorescence - Anti-Doublecortin antibody (ab18723)

  Doublecortin Immunocytochemistry/ Immunofluorescence staining of Rat Primary Neurons DIV1 cells using rabbit Anti-Doublecortin antibody

  ab18723 staining Doublecortin in Rt Primary Neurons DIV1 cells. The cells were fixed with 100% methanol (5 min) permeabilized with 0.1% PBS-Tween for 5 minutes and then blocked with 1% BSA/10% normal goat serum/0.3M glycine in 0.1%PBS-Tween for 1h. The cells were then incubated overnight at 4°C with ab18723 at 5µg/ml and Anti-alpha Tubulin antibody [DM1A] - Loading Control ab7291 Mouse monoclonal [DM1A] to alpha Tubulin - Loading Control. Cells were then incubated with Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081 Goat polyclonal Secondary Antibody to Rabbit IgG - H&L (Alexa Fluor^® 488) pre-adsorbed at 1/1000 dilution (shown in green) and Goat Anti-Mouse IgG H&L (Alexa Fluor® 594) preadsorbed ab150120 Goat polyclonal Secondary Antibody to Mouse IgG - H&L (Alexa Fluor^® 594) pre-adsorbed at 1/1000 dilution (shown in pseudocolour magenta). Nuclear DNA was labelled with DAPI (shown in blue).

  Also suitable in cells fixed with 4% paraformaldehyde (10 min).

  Image was acquired with a high-content analyser (Operetta CLS Perkin Elmer) and a maximum intensity projection of confocal sections is shown.

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  Immunohistochemistry (Frozen sections) - Anti-Doublecortin antibody (ab18723)

  Doublecortin Immunohistochemistry (Frozen sections) staining of 8 week old mouse dentate gyrus using rabbit Anti-Doublecortin antibody

  Immunofluorescence staining of Doublecortin in a section of frozen PFA perfusion fixed 8 week old mouse dentate gyrus.

  After dissection, the tissue was further fixed in PFA overnight, washed in PBS and then incubated overnight in 30% sucrose. It was then embedded in OCT and cryosectioned. No antigen retrieval step was performed prior to staining. Performed on a Leica BOND^TM. The section was incubated at room temperature for 1 hour with ab18723 at 1ug/mL and then incubated with Goat Anti-Rabbit IgG H&L (Alexa Fluor® 594) ab150080 (Goat Anti-Rabbit IgG H&L (Alexa Fluor® 594) preabsorbed, (Shown in magenta) 1/1000) for 1 hour at room temperature. Nuclear DNA was labelled with DAPI (shown in blue). The section was then mounted using Dako Fluorescence Mounting Medium^®.

  Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).

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