Date published: 2025-11-23

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DMPK Antibody (9-RY26): sc-134319

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Datasheets
  • DMPK Antibody (9-RY26) is a mouse monoclonal IgG2a κ DMPK antibody, cited in 4 publications, provided at 100 µg/ml
  • raised against an internal region of DMPK of human origin
  • recommended for detection of DMPK of human origin by WB, IP and ELISA
  • m-IgG Fc BP-HRP, m-IgG2a BP-HRP and m-IgGκ BP-HRP are the preferred secondary detection reagents for DMPK Antibody (9-RY26) for WB applications. These reagents are now offered in bundles with DMPK Antibody (9-RY26) (see ordering information below).

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DMPK Antibody (9-RY26) is a mouse monoclonal IgG2a kappa light chain antibody that detects the DMPK protein of human origin by western blotting (WB), immunoprecipitation (IP), and enzyme-linked immunosorbent assay (ELISA). Anti-DMPK antibody (9-RY26) is available as a non-conjugated format. Myotonic dystrophy protein kinase (DMPK) plays a crucial role in muscle function as a multi-domain protein kinase that is activated by G protein second messengers and proteolysis. DMPK involvement in myotonic muscular dystrophy (DM) makes this protein significant, as DM is a genetic disorder characterized by muscle weakness and cardiac conduction defects, primarily affecting skeletal and cardiac muscle. DM pathogenesis links to CTG repeat expansion in the 3′-untranslated region of the DMPK gene, leading to accumulation of mutant DMPK transcripts with extended CUG repeats retained in the nucleus. This retention disrupts normal cellular processes and influences the expression of the DM locus-associated homeodomain protein (DMAHP)/SIX5, contributing to clinical manifestations of the disease. DMPK interacts with various substrates, including myogenin, L-type calcium channels, and Phospholemman (PLM), highlighting DMPK′s multifaceted role in muscle physiology and pathology.

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

DMPK Antibody (9-RY26) References:

  1. DMPK dosage alterations result in atrioventricular conduction abnormalities in a mouse myotonic dystrophy model.  |  Berul, CI., et al. 1999. J Clin Invest. 103: R1-7. PMID: 10021468
  2. Phospholemman is a substrate for myotonic dystrophy protein kinase.  |  Mounsey, JP., et al. 2000. J Biol Chem. 275: 23362-7. PMID: 10811636
  3. Myotonic dystrophy protein kinase domains mediate localization, oligomerization, novel catalytic activity, and autoinhibition.  |  Bush, EW., et al. 2000. Biochemistry. 39: 8480-90. PMID: 10913253
  4. Reduced expression of DMAHP/SIX5 gene in myotonic dystrophy muscle.  |  Inukai, A., et al. 2000. Muscle Nerve. 23: 1421-6. PMID: 10951446
  5. Myotonic dystrophy in transgenic mice expressing an expanded CUG repeat.  |  Mankodi, A., et al. 2000. Science. 289: 1769-73. PMID: 10976074
  6. Fundamental aspects of DMPK optimization of targeted protein degraders.  |  Cantrill, C., et al. 2020. Drug Discov Today. 25: 969-982. PMID: 32298797
  7. The role of DMPK science in improving pharmaceutical research and development efficiency.  |  Mak, KK., et al. 2022. Drug Discov Today. 27: 705-729. PMID: 34774767
  8. High Resolution Analysis of DMPK Hypermethylation and Repeat Interruptions in Myotonic Dystrophy Type 1.  |  Rasmussen, A., et al. 2022. Genes (Basel). 13: PMID: 35741732
  9. ADME and DMPK considerations for the discovery and development of antibody drug conjugates (ADCs).  |  Beaumont, K., et al. 2022. Xenobiotica. 52: 770-785. PMID: 36314242
  10. Antisense oligonucleotide targeting DMPK in patients with myotonic dystrophy type 1: a multicentre, randomised, dose-escalation, placebo-controlled, phase 1/2a trial.  |  Thornton, CA., et al. 2023. Lancet Neurol. 22: 218-228. PMID: 36804094
  11. Specific DMPK-promoter targeting by CRISPRi reverses myotonic dystrophy type 1-associated defects in patient muscle cells.  |  Porquet, F., et al. 2023. Mol Ther Nucleic Acids. 32: 857-871. PMID: 37273786
  12. Altered phosphorylation and intracellular distribution of a (CUG)n triplet repeat RNA-binding protein in patients with myotonic dystrophy and in myotonin protein kinase knockout mice.  |  Roberts, R., et al. 1997. Proc Natl Acad Sci U S A. 94: 13221-6. PMID: 9371827

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

DMPK Antibody (9-RY26)

sc-134319
100 µg/ml
$333.00

DMPK Antibody (9-RY26): m-IgG Fc BP-HRP Bundle

sc-537366
100 µg Ab; 10 µg BP
$354.00

DMPK Antibody (9-RY26): m-IgGκ BP-HRP Bundle

sc-534613
100 µg Ab; 40 µg BP
$354.00

DMPK Antibody (9-RY26): m-IgG2a BP-HRP Bundle

sc-547994
100 µg Ab; 10 µg BP
$354.00

Bonjour, cette anticorps a t'il été validé pour la cytométrie en flux? Merci

Asked by: StemCell
Merci pour votre question. Cet anticorps est recommandé uniquement pour les tests WB, IP et ELISA.
Answered by: Tech Support Europe
Date published: 2025-10-23

For Western Blot, is it recommended to use denatured or non-denatured conditions with DMPK (9-RY26): sc-134319 antibody?

Asked by: jerojero
Thank you for your question. We recommend this antibody for use in denatured Western Blot conditions. It has not been validated for use in non-denatured conditions. Please contact our Technical Service Department for further details or inquiries.
Answered by: Technical Support
Date published: 2017-03-27
  • y_2025, m_11, d_22, h_6CST
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Rated 5 out of 5 by from Good for Western BlotAntibody detects over-expressed human DMPK in transfected lysate and endogenous DMPK in human cell lines HeLa, K-562, and Jurkat. -SCBT QC
Date published: 2023-09-14
Rated 4 out of 5 by from Good antibodyIt detects different forms of DMPK (phosphorylation variants) in western blots.
Date published: 2019-02-26
Rated 1 out of 5 by from No hay señalEl producto no nos funcionó, en cambio otros anticuerpos si.
Date published: 2017-08-29
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DMPK Antibody (9-RY26) is rated 3.3 out of 5 by 4.
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