Astana Biomed Group, an authorized Abcam distributor in Central Asia

Anti-VAMP2 antibody [EPR12790] (ab181869)

Key features and details

  • Produced recombinantly (animal-free) for high batch-to-batch consistency and long term security of supply
  • Rabbit monoclonal [EPR12790] to VAMP2
  • Suitable for: WB, ICC/IF, Flow Cyt, IP
  • Reacts with: Mouse, Rat, Human

Overview

  • Product name

    Anti-VAMP2 antibody [EPR12790]
    See all VAMP2 primary antibodies

  • Description

    Rabbit monoclonal [EPR12790] to VAMP2

  • Host species

    Rabbit

  • Tested Applications & Species

    Application Species
    Flow Cyt
    Human
    ICC/IF
    Human
    IP
    Human
    WB
    Mouse
    Rat
    Human
    See all applications and species data

  • Immunogen

    Synthetic peptide. This information is proprietary to Abcam and/or its suppliers.

  • Positive control

    • WB: Human fetal brain and Human cerebellum lysates ICC/IF: SH-SY5Y cells. Flow cyt: Jurkat cells.

  • General notes

    This product is a recombinant monoclonal antibody, which offers several advantages including:

    • - High batch-to-batch consistency and reproducibility
    • - Improved sensitivity and specificity
    • - Long-term security of supply
    • - Animal-free production
    For more information see here.

    Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.

    We are constantly working hard to ensure we provide our customers with best in class antibodies. As a result of this work we are pleased to now offer this antibody in purified format. We are in the process of updating our datasheets. The purified format is designated 'PUR' on our product labels. If you have any questions regarding this update, please contact our Scientific Support team.

Properties

Images

  • Western blot - Anti-VAMP2 antibody [EPR12790] (ab181869)
    Western blot - Anti-VAMP2 antibody [EPR12790] (ab181869)
    Anti-VAMP2 antibody [EPR12790] (ab181869) at 1/10000 dilution (purified) + Rat heart lysate at 10 µg

    Secondary
    Anti-Rabbit IgG (HRP), specific to the non-reduced form of IgG at 1/1000 dilution

    Predicted band size: 13 kDa



    Blocking buffer and concentration: 5% NFDM/TBST.
    Diluting buffer and concentration: 5% NFDM /TBST.

  • Immunocytochemistry/ Immunofluorescence - Anti-VAMP2 antibody [EPR12790] (ab181869)
    Immunocytochemistry/ Immunofluorescence - Anti-VAMP2 antibody [EPR12790] (ab181869)

    ab181869 staining VAMP2 in U87-MG (human glioblastoma) cells by ICC/IF (Immunocytochemistry/immunofluorescence). Cells were fixed with 100% methanol. Samples were incubated with primary antibody at a dilution of 1/500. A goat anti rabbit IgG (Alexa Fluor® 488) (ab150077) was used as the secondary antibody at a dilution of 1/1000. DAPI was used as a nuclear counterstain.

    Negative control 1:PBS only.

  • Immunocytochemistry/ Immunofluorescence - Anti-VAMP2 antibody [EPR12790] (ab181869)
    Immunocytochemistry/ Immunofluorescence - Anti-VAMP2 antibody [EPR12790] (ab181869)

    Immunofluorescent analysis of U87-MG cells (4% paraformaldehyde-fixed)  labeling VAMP2 with ab181869 at 1/500 dilution followed by Goat anti rabbit IgG (Alexa Fluor®488) at 1/200 dilution and counterstained with Dapi.

  • Flow Cytometry - Anti-VAMP2 antibody [EPR12790] (ab181869)
    Flow Cytometry - Anti-VAMP2 antibody [EPR12790] (ab181869)

    Flow cytometry analysis of Jurkat cells fixed with 2% paraformaldehyde labeling VAMP2 with unpurified ab181869 at 1/150 dilution followed by Goat anti rabbit IgG (FITC) at 1/150 dilution. Rabbit monoclonal IgG was used as an isotype control.

  • Western blot - Anti-VAMP2 antibody [EPR12790] (ab181869)
    Western blot - Anti-VAMP2 antibody [EPR12790] (ab181869)
    Anti-VAMP2 antibody [EPR12790] (ab181869) at 1/50000 dilution (purified) + Mouse brain lysate at 10 µg

    Secondary
    Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/100000 dilution (Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated)

    Predicted band size: 13 kDa



    Blocking buffer and concentration: 5% NFDM/TBST.
    Diluting buffer and concentration: 5% NFDM /TBST.

  • Western blot - Anti-VAMP2 antibody [EPR12790] (ab181869)
    Western blot - Anti-VAMP2 antibody [EPR12790] (ab181869)
    Anti-VAMP2 antibody [EPR12790] (ab181869) at 1/50000 dilution (purified) + Human cerebellum lysate at 10 µg

    Secondary
    Anti-Rabbit IgG (HRP), specific to the non-reduced form of IgG at 1/10000 dilution

    Predicted band size: 13 kDa



    Blocking buffer and concentration: 5% NFDM/TBST.
    Diluting buffer and concentration: 5% NFDM /TBST.

  • Western blot - Anti-VAMP2 antibody [EPR12790] (ab181869)
    Western blot - Anti-VAMP2 antibody [EPR12790] (ab181869)
    All lanes : Anti-VAMP2 antibody [EPR12790] (ab181869) at 1/50000 dilution (unpurified)

    Lane 1 : Human fetal brain lysate
    Lane 2 : Human cerebellum lysate

    Lysates/proteins at 10 µg per lane.

    Secondary
    All lanes : Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugate at 1/1000 dilution

    Predicted band size: 13 kDa

  • Immunoprecipitation - Anti-VAMP2 antibody [EPR12790] (ab181869)
    Immunoprecipitation - Anti-VAMP2 antibody [EPR12790] (ab181869)

    ab181869 (purified) at 1/150 immunoprecipitating VAMP2 in Human cerebellum whole cell lysate. 10 ug of cell lysate was present in the input. For western blotting, a HRP-conjugated Veriblot for IP Detection Reagent (ab131366) (1/1,500) was used for detection. A rabbit monoclonal IgG (ab172730) was used intead of ab128913 as a negative control (Lane 3).

    Blocking buffer and concentration: 5% NFDM/TBST.

    Diluting buffer and concentration: 5% NFDM /TBST.

  • Immunoprecipitation - Anti-VAMP2 antibody [EPR12790] (ab181869)
    Immunoprecipitation - Anti-VAMP2 antibody [EPR12790] (ab181869)

    Western blot analysis of immunoprecipitation pellet from Human cerebellum lysate immunoprecipitated using ab181869 at 1/70 dilution.
    Secondary: Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugate at 1/1000 dilution.

  • Flow Cytometry - Anti-VAMP2 antibody [EPR12790] (ab181869)
    Flow Cytometry - Anti-VAMP2 antibody [EPR12790] (ab181869)

    Flow Cytometry analysis of SH-SY5Y cells labelling VAMP2 with purified ab181869 at 1/100 (red). Cells were fixed with 4% paraformaldehyde. A FITC-conjugated goat anti-rabbit IgG (1/500) was used as the secondary antibody. Black - Isotype control, rabbit monoclonal IgG. Blue - Unlabelled control, cells without incubation with primary and secondary antibodies.

  • Immunocytochemistry/ Immunofluorescence - Anti-VAMP2 antibody [EPR12790] (ab181869)
    Immunocytochemistry/ Immunofluorescence - Anti-VAMP2 antibody [EPR12790] (ab181869)

    Immunocytochemistry/Immunofluorescence analysis of U87-MG (human glioblastoma) cells labelling VAMP2 with purified ab181869 at 1/250. Cells were fixed with 100% methanol and permeabilized with 0.1% Triton X-100. ab150077, an Alexa Fluor® 488-conjugated goat anti-rabbit IgG (1/1000) was used as the secondary antibody. DAPI (blue) was used as the nuclear counterstain. ab7291, a mouse anti-tubulin (1/1000) and ab150120, an Alexa Fluor® 594-conjugated goat anti-mouse IgG (1/1000) were also used.

    Control 1: primary antibody (1/100) and secondary antibody, ab150120, an Alexa Fluor® 594-conjugated goat anti-mouse IgG (1/500).

    Control 2: ab7291 (1/1000) and secondary antibody, ab150077, an Alexa Fluor® 488-conjugated goat anti-rabbit IgG (1/500).

  • Immunocytochemistry/ Immunofluorescence - Anti-VAMP2 antibody [EPR12790] (ab181869)
    Immunocytochemistry/ Immunofluorescence - Anti-VAMP2 antibody [EPR12790] (ab181869)

    Immunofluorescent analysis of SH-SYSY cells (human cell line) (4% paraformaldehyde-fixed) labeling VAMP2 with unpurified ab181869 at 1/500 dilution followed by Goat anti rabbit IgG (Alexa Fluor®488) at 1/200 dilution and counterstained with DAPI.

  • Anti-VAMP2 antibody [EPR12790] (ab181869)
    Anti-VAMP2 antibody [EPR12790] (ab181869)

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