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Signal Transduction Cytoskeleton / ECM Extracellular Matrix Structures Focal Adhesions
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Anti-VASP antibody [OTI1H8] (ab114029)

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Western blot - Anti-VASP antibody [OTI1H8] (ab114029)
  • Immunocytochemistry/ Immunofluorescence - Anti-VASP antibody [OTI1H8] (ab114029)
  • Flow Cytometry - Anti-VASP antibody [OTI1H8] (ab114029)
  • Western blot - Anti-VASP antibody [OTI1H8] (ab114029)

Key features and details

  • Mouse monoclonal [OTI1H8] to VASP
  • Suitable for: WB, Flow Cyt, ICC/IF
  • Reacts with: Dog, Human, African green monkey
  • Isotype: IgG1

You may also be interested in

Protein
Product image
Recombinant Human VASP protein (ab105601)
Secondary
Product image
Goat Anti-Mouse IgG H&L (HRP) (ab205719)

View more associated products

Overview

  • Product name

    Anti-VASP antibody [OTI1H8]
    See all VASP primary antibodies
  • Description

    Mouse monoclonal [OTI1H8] to VASP
  • Host species

    Mouse
  • Tested Applications & Species

    Application Species
    Flow Cyt
    Human
    ICC/IF
    African green monkey
    WB
    Human
    See all applications and species data
  • Immunogen

    Recombinant full length protein corresponding to Human VASP aa 1 to the C-terminus. Produced in HEK-293T cells. NP_003361
    Database link: P50552

    Run BLAST with BLAST the sequence with ExPASy Run BLAST with BLAST the sequence with NCBI
  • Positive control

    • WB: HEK-293T cell lysate transfected with pCMV6-ENTRY VASP cDNA; HepG2, HeLa, MCF7, HT-29 and A549 cell extracts; ICC/IF: COS-7 cells transiently transfected by pCMV6-ENTRY VASP; Flow Cyt: HEK-293T cells transfected with pCMV6-ENTRY VASP overexpress plasmid.
  • General notes

    The clone number has been updated from 1H8 to OTI1H8, both clone numbers name the same clone.

Properties

  • Form

    Liquid
  • Storage instructions

    Shipped at 4°C. Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C. Avoid freeze / thaw cycle.
  • Storage buffer

    pH: 7.30
    Preservative: 0.02% Sodium azide
    Constituents: PBS, 1% BSA, 50% Glycerol
  • Concentration information loading...
  • Purity

    Affinity purified
  • Purification notes

    Purified from cell culture supernatant by affinity chromatography
  • Clonality

    Monoclonal
  • Clone number

    OTI1H8
  • Isotype

    IgG1
  • Research areas

    • Signal Transduction
    • Cytoskeleton / ECM
    • Extracellular Matrix
    • Structures
    • Focal Adhesions

Associated products

  • Compatible Secondaries

    • Goat Anti-Mouse IgG H&L (Alexa Fluor® 488) (ab150113)
    • Goat Anti-Mouse IgG H&L (HRP) (ab205719)
  • Isotype control

    • Mouse IgG1, kappa monoclonal [15-6E10A7] - Isotype Control (ab170190)
  • Positive Controls

    • HeLa whole cell lysate (ab150035)
    • Hep G2 whole cell lysate (ab166833)
    • MCF7 whole cell lysate (ab29537)
    • HeLa whole cell lysate (ab29545)
    • HT-29 whole cell lysate (ab3952)
    • A549 whole cell lysate (ab7910)
  • Recombinant Protein

    • Recombinant Human VASP protein (ab105601)

Applications

The Abpromise guarantee

Our Abpromise guarantee covers the use of ab114029 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

Guaranteed

Tested applications are guaranteed to work and covered by our Abpromise guarantee.

Predicted

Predicted to work for this combination of applications and species but not guaranteed.

Incompatible

Does not work for this combination of applications and species.

Application Species
Flow Cyt
Human
ICC/IF
African green monkey
WB
Human
Application Abreviews Notes
WB
1/500 - 1/2000. Predicted molecular weight: 40 kDa.
Flow Cyt
1/100.

ab170190 - Mouse monoclonal IgG1, is suitable for use as an isotype control with this antibody.

ICC/IF
1/100.
Notes
WB
1/500 - 1/2000. Predicted molecular weight: 40 kDa.
Flow Cyt
1/100.

ab170190 - Mouse monoclonal IgG1, is suitable for use as an isotype control with this antibody.

ICC/IF
1/100.

Target

  • Function

    Ena/VASP proteins are actin-associated proteins involved in a range of processes dependent on cytoskeleton remodeling and cell polarity such as axon guidance, lamellipodial and filopodial dynamics, platelet activation and cell migration. VASP promotes actin filament elongation. It protects the barbed end of growing actin filaments against capping and increases the rate of actin polymerization in the presence of capping protein. VASP stimulates actin filament elongation by promoting the transfer of profilin-bound actin monomers onto the barbed end of growing actin filaments. Plays a role in actin-based mobility of Listeria monocytogenes in host cells. Regulates actin dynamics in platelets and plays an important role in regulating platelet aggregation.
  • Tissue specificity

    Highly expressed in platelets.
  • Sequence similarities

    Belongs to the Ena/VASP family.
    Contains 1 WH1 domain.
  • Domain

    The EVH2 domain is comprised of 3 regions. Block A is a thymosin-like domain required for G-actin binding. The KLKR motif within this block is essential for the G-actin binding and for actin polymerization. Block B is required for F-actin binding and subcellular location, and Block C for tetramerization.
    The WH1 domain mediates interaction with XIRP1.
  • Post-translational
    modifications

    Major substrate for cAMP-dependent (PKA) and cGMP-dependent protein kinase (PKG) in platelets. The preferred site for PKA is Ser-157, the preferred site for PKG, Ser-239. In ADP-activated platelets, phosphorylation by PKA or PKG on Ser-157 leads to fibrinogen receptor inhibition. Phosphorylation on Thr-278 requires prior phosphorylation on Ser-157 and Ser-239. In response to phorbol ester (PMA) stimulation, phosphorylated by PKC/PRKCA. In response to thrombin, phosphorylated by both PKC and ROCK1. Phosphorylation at Thr-278 by AMPK does not require prior phosphorylation at Ser-157 or Ser-239. Phosphorylation modulates F-actin binding, actin filament elongation and platelet activation. Carbon monoxide (CO) promotes phosphorylation at Ser-157, while nitric oxide (NO) promotes phosphorylation at Ser-157, but also at Ser-239. Response to NO and CO is blunted in platelets from diabetic patients, and VASP is not phosphorylated efficiently at Ser-157 and Ser-239.
  • Cellular localization

    Cytoplasm. Cytoplasm > cytoskeleton. Cell junction > focal adhesion. Cell projection > lamellipodium membrane. Cell projection > filopodium membrane. Targeted to stress fibers and focal adhesions through interaction with a number of proteins including MRL family members. Localizes to the plasma membrane in protruding lamellipodia and filopodial tips. Stimulation by thrombin or PMA, also translocates VASP to focal adhesions. Localized along the sides of actin filaments throughout the peripheral cytoplasm under basal conditions.
  • Target information above from: UniProt accession P50552 The UniProt Consortium
    The Universal Protein Resource (UniProt) in 2010
    Nucleic Acids Res. 38:D142-D148 (2010) .

    Information by UniProt
  • Database links

    • Entrez Gene: 403936 Dog
    • Entrez Gene: 7408 Human
    • Omim: 601703 Human
    • SwissProt: P50551 Dog
    • SwissProt: P50552 Human
    • Unigene: 515469 Human
    • Alternative names

      • Vasodilator stimulated phosphoprotein antibody
      • Vasodilator-stimulated phosphoprotein antibody
      • VASP antibody
      • VASP_HUMAN antibody

    Images

    • Western blot - Anti-VASP antibody [OTI1H8] (ab114029)
      Western blot - Anti-VASP antibody [OTI1H8] (ab114029)
      All lanes : Anti-VASP antibody [OTI1H8] (ab114029) at 1/500 dilution

      Lane 1 : HepG2 (Human liver hepatocellular carcinoma cell line) cell extract
      Lane 2 : HeLa (Human epithelial cell line from cervix adenocarcinoma) cell extract
      Lane 3 : HT-29 (Human colorectal adenocarcinoma cell line) cell extract
      Lane 4 : A549 (Human lung carcinoma cell line) cell extract
      Lane 5 : COS-7 (African green monkey kidney fibroblast-like cell line) cell extract
      Lane 6 : Jurkat (Human T cell leukemia cell line from peripheral blood) cell extract
      Lane 7 : MDCK (Canine kidney cell line) cell extract
      Lane 8 : PC-12 (Rat adrenal gland pheochromocytoma cell line) cell extract
      Lane 9 : MCF7 (Human breast adenocarcinoma cell line) cell extract

      Lysates/proteins at 35 µg per lane.

      Predicted band size: 40 kDa

    • Immunocytochemistry/ Immunofluorescence - Anti-VASP antibody [OTI1H8] (ab114029)
      Immunocytochemistry/ Immunofluorescence - Anti-VASP antibody [OTI1H8] (ab114029)

      ab114029 at 1/100 dilution staining VASP in COS-7 (African green monkey kidney fibroblast-like cell line) cells transiently transfected with pCMV6-ENTRY VASP by Immunofluorescence.

    • Flow Cytometry - Anti-VASP antibody [OTI1H8] (ab114029)
      Flow Cytometry - Anti-VASP antibody [OTI1H8] (ab114029)

      ab114029 at 1/100 dilution staining VASP in HEK-293T (Human epithelial cell line from embryonic kidney transformed with large T antigen) cells transfected with either pCMV6-ENTRY VASP overexpress plasmid (Red) or empty vector control plasmid (Blue) by flow cytometry.

    • Western blot - Anti-VASP antibody [OTI1H8] (ab114029)
      Western blot - Anti-VASP antibody [OTI1H8] (ab114029)
      All lanes : Anti-VASP antibody [OTI1H8] (ab114029) at 1/500 dilution

      Lane 1 : HEK-293T (Human epithelial cell line from embryonic kidney transformed with large T antigen) cell lysate transfected with pCMV6-ENTRY control cDNA
      Lane 2 : HEK-293T cell lysate transfected with pCMV6-ENTRY VASP cDNA

      Lysates/proteins at 5 µg per lane.

      Predicted band size: 40 kDa

    Protocols

    To our knowledge, customised protocols are not required for this product. Please try the standard protocols listed below and let us know how you get on.

    Click here to view the general protocols

    Datasheets and documents

    • Datasheet
  • References (0)

    Publishing research using ab114029? Please let us know so that we can cite the reference in this datasheet.

    ab114029 has not yet been referenced specifically in any publications.

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