Date published: 2025-12-10

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α-dystroglycan Antibody (2237E2D1): sc-65628

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Datasheets
  • α-dystroglycan Antibody (2237E2D1) is a mouse monoclonal IgG2b κ provided at 200 µg/ml
  • raised against brain tissue homogenate, with epitope mapping to the glycosylation site of α-dystroglycan of bovine origin
  • recommended for detection of brain α-dystroglycan of bovine origin by WB and IP; non cross-reactive with brain α-dystroglycan of mouse, rat and rabbit origin; non cross reactive with skeletal muscle α-dystroglycan
  • See α-dystroglycan (IIH6): sc-53987 for α-dystroglycan antibody conjugates, including AC, HRP, FITC, PE, Alexa Fluor® 488, 594, 647, 680 and 790.
  • m-IgG Fc BP-HRP is the preferred secondary detection reagent for α-dystroglycan Antibody (2237E2D1) for WB applications. This reagent is now offered in a bundle with α-dystroglycan Antibody (2237E2D1) (see ordering information below).

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    α-dystroglycan Antibody (2237E2D1) is a mouse monoclonal IgG2b antibody that detects α-dystroglycan in bovine samples through western blotting (WB) and immunoprecipitation (IP) applications. α-dystroglycan (2237E2D1) antibody recognizes a crucial cell surface receptor that interacts with various extracellular matrix molecules, including laminins, Agrin, and Perlecan, playing a vital role in the formation of basement membranes during early development and the organization of laminin on the cell surface. α-dystroglycan monoclonal antibody (2237E2D1) targets a protein primarily located on the cell membrane, where α-dystroglycan forms a complex with the transmembrane glycoprotein β-dystroglycan, creating the α/β-dystroglycan complex essential for maintaining muscle integrity and function. Anti-α-dystroglycan antibody (2237E2D1) detects a protein integral to the dystrophin-associated protein complex at the sarcolemma and the utrophin-associated protein complex at the neuromuscular junction, facilitating the clustering of nicotinic acetylcholine receptors, which is critical for effective neuromuscular transmission. Proper functioning of α-dystroglycan is essential for muscle cell stability and signaling, making α-dystroglycan a significant target for research in muscle-related diseases and developmental biology.

    For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.

    Alexa Fluor® is a trademark of Molecular Probes Inc., OR., USA

    LI-COR® and Odyssey® are registered trademarks of LI-COR Biosciences

    α-dystroglycan Antibody (2237E2D1) References:

    1. Deficiency of alpha-dystroglycan in muscle-eye-brain disease.  |  Kano, H., et al. 2002. Biochem Biophys Res Commun. 291: 1283-6. PMID: 11883957
    2. Aberrant glycosylation of alpha-dystroglycan and congenital muscular dystrophies.  |  Endo, T. 2005. Acta Myol. 24: 64-9. PMID: 16550917
    3. Defective glycosylation of α-dystroglycan contributes to podocyte flattening.  |  Kojima, K., et al. 2011. Kidney Int. 79: 311-6. PMID: 20944549
    4. Decoding arenavirus pathogenesis: essential roles for alpha-dystroglycan-virus interactions and the immune response.  |  Oldstone, MB. and Campbell, KP. 2011. Virology. 411: 170-9. PMID: 21185048
    5. Dissecting the molecular basis of the role of the O-mannosylation pathway in disease: α-dystroglycan and forms of muscular dystrophy.  |  Live, D., et al. 2013. Chembiochem. 14: 2392-402. PMID: 24318691
    6. Chemoenzymatic synthesis of α-dystroglycan core M1 O-mannose glycans.  |  Zhang, Y., et al. 2015. Chem Commun (Camb). 51: 11654-7. PMID: 26100261
    7. Exogenous expression of the glycosyltransferase LARGE1 restores α-dystroglycan matriglycan and laminin binding in rhabdomyosarcoma.  |  Beltrán, D., et al. 2019. Skelet Muscle. 9: 11. PMID: 31054580
    8. HNK-1 sulfotransferase modulates α-dystroglycan glycosylation by 3-O-sulfation of glucuronic acid on matriglycan.  |  Sheikh, MO., et al. 2020. Glycobiology. 30: 817-829. PMID: 32149355
    9. Cancer Malignancy Is Correlated with Upregulation of PCYT2-Mediated Glycerol Phosphate Modification of α-Dystroglycan.  |  Umezawa, F., et al. 2022. Int J Mol Sci. 23: PMID: 35743105
    10. Identification of Matriglycan by Dual Exoglycosidase Digestion of α-Dystroglycan.  |  Chandel, I. and Campbell, KP. 2023. Bio Protoc. 13: e4827. PMID: 37753476

    Ordering Information

    Product NameCatalog #UNITPriceQtyFAVORITES

    α-dystroglycan Antibody (2237E2D1)

    sc-65628
    200 µg/ml
    $316.00

    α-dystroglycan Antibody (2237E2D1): m-IgG Fc BP-HRP Bundle

    sc-539186
    200 µg Ab; 10 µg BP
    $354.00

    How much sample do you recommend loading on the gel for Western blot detection using α-dystroglycan (2237E2D1): sc-65628?

    Asked by: TinTin
    We recommend loading 40–60 µg whole cell lysate, 10–20 µg nuclear extract, 5-10 µg transfected lysate, or 10–20 ng purified protein per lane. A link to our complete Western blotting protocol is provided here for your reference: https://www.scbt.com/scbt/resources/protocols/western-immuno-blotting
    Answered by: Technical Support
    Date published: 2017-03-01
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    Rated 4 out of 5 by from Strong positive signal observed in WB inStrong positive signal observed in WB in cow brain tissue extract. -SCBT QC
    Date published: 2014-05-27
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    α-dystroglycan Antibody (2237E2D1) is rated 4.0 out of 5 by 1.
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