Date published: 2026-6-4

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dystrophin Antibody (MANDRA1): sc-73592

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  • dystrophin Antibody (MANDRA1) is a mouse monoclonal IgG1 κ dystrophin antibody, cited in 10 publications, provided at 200 µg/ml
  • raised against amino acids 3200-3684 dystrophin of human origin
  • recommended for detection of an epitope corresponding to amino acids 3558-3684 of dystrophin of mouse, rat, human and fish origin by WB, IP, IF and IHC(P)
  • available conjugated to agarose for IP; HRP for WB, IHC(P) and ELISA; and to either phycoerythrin or FITC for IF, IHC(P) and FCM
  • also available conjugated to Alexa Fluor® 488 or Alexa Fluor® 647 for IF, IHC(P) and FCM
  • m-IgG Fc BP-HRP and m-IgG1 BP-HRP are the preferred secondary detection reagents for dystrophin Antibody (MANDRA1) for WB and IHC(P) applications. These reagents are now offered in bundles with dystrophin Antibody (MANDRA1) (see ordering information below).
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Dystrophin Antibody (MANDRA1) is a mouse monoclonal IgG1 kappa light chain antibody that detects dystrophin protein of mouse, rat, and human origin by western blotting (WB), immunoprecipitation (IP), immunofluorescence (IF), and immunohistochemistry. Anti-dystrophin antibody (MANDRA1) is available in both non-conjugated and various conjugated forms, including agarose, horseradish peroxidase (HRP), phycoerythrin (PE), fluorescein isothiocyanate (FITC), and multiple Alexa Fluor® conjugates. Dystrophin plays a crucial role in the dystrophin-glycoprotein complex (DGC), which connects the F-actin cytoskeleton within muscle fibers to the extracellular matrix, thereby maintaining the structural integrity of muscle cells during contraction. This connection is vital for muscle function, as it helps to stabilize the muscle membrane and prevent damage during mechanical stress. A deficiency in dystrophin is linked to severe muscle disorders such as Duchenne (DMD) and Becker (BMD) muscular dystrophies, highlighting dystrophin′s importance in muscle health. The human dystrophin gene spans 2.4 megabases, contains over 80 exons, and produces a 14 kb mRNA that can undergo differential splicing to generate a variety of transcripts, each encoding different protein isoforms. Dystrophin constitutes approximately 0.002% of total striated muscle protein and is localized at triadic junctions in skeletal muscle, where dystrophin is believed to play a significant role in calcium ion homeostasis and force transmission, further underscoring dystrophin′s importance in muscle physiology.

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

dystrophin Antibody (MANDRA1) References:

  1. Dystrophin is a microtubule-associated protein.  |  Prins, KW., et al. 2009. J Cell Biol. 186: 363-9. PMID: 19651889
  2. Skipping multiple exons of dystrophin transcripts using cocktail antisense oligonucleotides.  |  Echigoya, Y. and Yokota, T. 2014. Nucleic Acid Ther. 24: 57-68. PMID: 24380394
  3. Dystrophin quantification: Biological and translational research implications.  |  Anthony, K., et al. 2014. Neurology. 83: 2062-9. PMID: 25355828
  4. Dystrophin Analysis in Clinical Trials.  |  Aartsma-Rus, A. 2014. J Neuromuscul Dis. 1: 41-53. PMID: 27858668
  5. Utrophin Compensates dystrophin Loss during Mouse Spermatogenesis.  |  Chen, HC., et al. 2017. Sci Rep. 7: 7372. PMID: 28785010
  6. Dystrophin Dp71 Subisoforms Localize to the Mitochondria of Human Cells.  |  Niba, ETE., et al. 2021. Life (Basel). 11: PMID: 34575126
  7. Dystrophin in the Neonatal and Adult Rat Intestine.  |  Lionarons, JM., et al. 2021. Life (Basel). 11: PMID: 34833031
  8. The role of dystrophin isoforms and interactors in the brain.  |  Tetorou, K., et al. 2024. Brain.. PMID: 39673425
  9. Dystrophin-associated proteins in muscular dystrophy.  |  Ozawa, E., et al. 1995. Hum Mol Genet. 4 Spec No: 1711-6. PMID: 8541869
  10. Structure-function relationships in dystrophin and utrophin.  |  Winder, SJ. 1996. Biochem Soc Trans. 24: 497-501. PMID: 8736791

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

dystrophin Antibody (MANDRA1)

sc-73592
200 µg/ml
$322.00

dystrophin Antibody (MANDRA1): m-IgG Fc BP-HRP Bundle

sc-527006
200 µg Ab; 10 µg BP
$361.00

dystrophin Antibody (MANDRA1): m-IgG1 BP-HRP Bundle

sc-532379
200 µg Ab; 20 µg BP
$361.00

dystrophin Antibody (MANDRA1) AC

sc-73592 AC
500 µg/ml, 25% agarose
$424.00

dystrophin Antibody (MANDRA1) HRP

sc-73592 HRP
200 µg/ml
$322.00

dystrophin Antibody (MANDRA1) FITC

sc-73592 FITC
200 µg/ml
$336.00

dystrophin Antibody (MANDRA1) PE

sc-73592 PE
200 µg/ml
$349.00

dystrophin Antibody (MANDRA1) Alexa Fluor® 488

sc-73592 AF488
200 µg/ml
$364.00

dystrophin Antibody (MANDRA1) Alexa Fluor® 647

sc-73592 AF647
200 µg/ml
$364.00

can i use dystrophin Antibody (MANDRA1): sc-73592 to IP the dystrophin from the rabbit muscle?

Asked by: bingo
Thank you for your question. Yes sc-73592 can be used for IP. https://www.scbt.com/resources/protocols/immunoprecipitation-western-blots
Answered by: BlakeJ
Date published: 2023-05-31

Can dystrophin (MANDRA1): sc-73592 monoclonal antibody be used in IF or IHC with mouse tissue or cells? Will there be non-specific staining?

Asked by: Professor Griffin
Thank you for your inquiry. The use of mouse monoclonal antibodies with mouse samples is very common and typically poses no problem. To eliminate any potential cross-reactivity of an anti-mouse secondary detection reagent, dystrophin (MANDRA1): sc-73592 is available in a variety of direct conjugations, such as HRP, PE, FITC and AlexaFluors.
Answered by: Technical Support
Date published: 2017-02-24
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Rated 4 out of 5 by from recognizes Dp71 isoform of dystrophinwe were interested in this sample to detect Dp71 isoform of dystrophin. It works fine in WB, IP and IF. for WB the final concentration was 1:1000 (or 0.2ug/ml) in TBST. For blocking I used 5% milk in TBST. For IP I used 1ug of AB and 2mg of lysate. It also works fine in coIP. for IF I used 1:100 final dilution of AB.
Date published: 2018-08-27
Rated 5 out of 5 by from Great !This antibody (sc-73592, 1:333 dilution) works well with dystrophin proteins in skeletal muscle tissues, including Quadriceps (Q), Gastrocnemius (G) and Tibialis Anterior (T), of normal mouse. Mdx tissue lysates are negative controls.
Date published: 2017-09-05
Rated 5 out of 5 by from Great for Paraffin Sections!Excellent choice when working with paraffin-embedded sections in IHC.
Date published: 2017-01-18
Rated 5 out of 5 by from Excellent immunoperoxidase membrane and cytoplasmicExcellent immunoperoxidase membrane and cytoplasmic staining in formalin fixed, paraffin-embedded human heart muscle tissue. -SCBT QC
Date published: 2015-04-06
Rated 5 out of 5 by from Band of interest observed in WB in both humanBand of interest observed in WB in both human skeletal muscle and rat skeletal muscle issue extracts. -SCBT QC
Date published: 2015-03-31
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dystrophin Antibody (MANDRA1) is rated 4.8 out of 5 by 5.
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