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    products/primary-antibodies/ellis-van-creveld-syndrome-antibody-epr10408-ab171952.pdf

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RecombinantRabMAb

Recombinant Anti-Ellis van Creveld syndrome antibody [EPR10408] (ab171952)

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Western blot - Anti-Ellis van Creveld syndrome antibody [EPR10408] (ab171952)
  • Immunocytochemistry/ Immunofluorescence - Anti-Ellis van Creveld syndrome antibody [EPR10408] (ab171952)
  • Anti-Ellis van Creveld syndrome antibody [EPR10408] (ab171952)

Key features and details

  • Produced recombinantly (animal-free) for high batch-to-batch consistency and long term security of supply
  • Rabbit monoclonal [EPR10408] to Ellis van Creveld syndrome
  • Suitable for: WB, ICC/IF
  • Reacts with: Human

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Overview

  • Product name

    Anti-Ellis van Creveld syndrome antibody [EPR10408]
    See all Ellis van Creveld syndrome primary antibodies
  • Description

    Rabbit monoclonal [EPR10408] to Ellis van Creveld syndrome
  • Host species

    Rabbit
  • Tested applications

    Suitable for: WB, ICC/IFmore details
    Unsuitable for: Flow Cyt,IHC-P or IP
  • Species reactivity

    Reacts with: Human
    Predicted to work with: Mouse, Rat
  • Immunogen

    Synthetic peptide within Human Ellis van Creveld syndrome aa 200-300 (Cysteine residue). The exact sequence is proprietary.
    Database link: P57679

  • Positive control

    • MCF7, K562, HeLa and 293T cell lysates. HeLa 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

  • Form

    Liquid
  • Storage instructions

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

    pH: 7.20
    Constituents: 0.35% Sodium citrate, 0.17% Sodium chloride, 0.03% EDTA, 59% PBS, 40% Glycerol (glycerin, glycerine), 0.05% BSA
  • Concentration information loading...
  • Purity

    Protein A purified
  • Clonality

    Monoclonal
  • Clone number

    EPR10408
  • Isotype

    IgG
  • Research areas

    • Developmental Biology
    • Organogenesis
    • Skeletal development
    • Muscle
    • Developmental Biology
    • Organogenesis
    • Skeletal development
    • Bone

Associated products

  • Alternative Versions

    • Anti-Ellis van Creveld syndrome antibody [EPR10408] - BSA and Azide free (ab249669)
  • Isotype control

    • Rabbit IgG, monoclonal [EPR25A] - Isotype Control (ab172730)
  • Positive Controls

    • HeLa whole cell lysate (ab150035)
    • HeLa whole cell lysate (ab29545)
    • K-562 whole cell lysate (ab7911)

Applications

The Abpromise guarantee

Our Abpromise guarantee covers the use of ab171952 in the following tested applications.

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

Application Abreviews Notes
WB
1/1000 - 1/5000. Predicted molecular weight: 112 kDa.
ICC/IF
1/50 - 1/100.
Notes
WB
1/1000 - 1/5000. Predicted molecular weight: 112 kDa.
ICC/IF
1/50 - 1/100.
Application notes
Is unsuitable for Flow Cyt,IHC-P or IP.

Target

  • Relevance

    Ellis van Creveld syndrome is an autosomal recessive disorder characterized by the clinical tetrad of chondrodystrophy, polydactyly, ectodermal dysplasia and cardiac anomalies. Patients manifest short limb dwarfism, short ribs, postaxial polydactyly and dysplastic nails and teeth. Congenital heart defects, most commonly an atrioventricular septal defect, are observed in 60% of affected individuals. Defects in this protein are a cause of Ellis van Creveld syndrome (EVC).
  • Cellular localization

    Membrane; Single pass membrane protein
  • Database links

    • Entrez Gene: 2121 Human
    • Entrez Gene: 59056 Mouse
    • Entrez Gene: 289712 Rat
    • Omim: 225500 Human
    • Omim: 604831 Human
    • SwissProt: P57679 Human
    • SwissProt: P57680 Mouse
    • Alternative names

      • DWF 1 antibody
      • DWF1 antibody
      • Ellis van Creveld syndrome protein antibody
      • EVC antibody
      • EVC1 antibody
      • EVCL antibody
      • MGC105107 antibody
      see all

    Images

    • Western blot - Anti-Ellis van Creveld syndrome antibody [EPR10408] (ab171952)
      Western blot - Anti-Ellis van Creveld syndrome antibody [EPR10408] (ab171952)
      All lanes : Anti-Ellis van Creveld syndrome antibody [EPR10408] (ab171952) at 1/1000 dilution

      Lane 1 : MCF7 cell lysate
      Lane 2 : K562 cell lysate
      Lane 3 : HeLa cell lysate
      Lane 4 : 293T cell lysate

      Lysates/proteins at 10 µg per lane.

      Predicted band size: 112 kDa

    • Immunocytochemistry/ Immunofluorescence - Anti-Ellis van Creveld syndrome antibody [EPR10408] (ab171952)
      Immunocytochemistry/ Immunofluorescence - Anti-Ellis van Creveld syndrome antibody [EPR10408] (ab171952)

      Immunofluorescent analysis of HeLa cells labeling Ellis van Creveld syndrome  with ab171952 at 1/50 dilution (red). DAPI nuclear staining (blue).

    • Anti-Ellis van Creveld syndrome antibody [EPR10408] (ab171952)
      Anti-Ellis van Creveld syndrome antibody [EPR10408] (ab171952)

    Protocols

    • Western blot protocols
    • Immunocytochemistry & immunofluorescence protocols

    Click here to view the general protocols

    Datasheets and documents

    • SDS download

    • Datasheet download

      Download

    References (0)

    Publishing research using ab171952? Please let us know so that we can cite the reference in this datasheet.

    ab171952 has not yet been referenced specifically in any publications.

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