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Browse our Dystrophin (DMD) ELISA Kits

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Dystrophin ELISA Kits (DMD)
On are 42 Dystrophin (DMD) ELISA Kits from 9 different suppliers available. Additionally we are shipping Dystrophin Antibodies (101) and Dystrophin Proteins (7) and many more products for this protein. A total of 155 Dystrophin products are currently listed.
BMD, cb664, CG7240, CG7243, CG7344, CG17750, CG31175, CG34157, CMD3B, det, DKFZp459C1629, DKFZp468A1620, DLP, DLP1, DLP2, DLP3, DLP186, dmd, dmDLP, dmDp186, dmDys, Dmel\\CG34157, DNADMD1, Dp71, Dp117, Dp186, Dp205, Dp427, DXS142, DXS164, DXS206, DXS230, DXS239, DXS268, DXS269, DXS270, DXS272, DXSmh7, DXSmh9, dys, GI3046716, IDLP, im:6911785, mdx, MGC79631, MGC83347, pke, RATDMD, zfDYS, zgc:110165
list all ELISA KIts Gene Name GeneID UniProt
DMD 1756 P11532
DMD 24907  
DMD 13405 P11531

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More ELISA Kits for Dystrophin Interaction Partners

Xenopus laevis Dystrophin (DMD) interaction partners

  1. Ordered disorder of the astrocytic dystrophin-associated protein complex in the norm and pathology.

Zebrafish Dystrophin (DMD) interaction partners

  1. Forced expression of embryonic dystrophin in zebrafish using an exon-skipping approach severely impairs the mobility and muscle architecture.

  2. Spatio-temporal differences in dystrophin dynamics at mRNA and protein levels have been revealed using a novel reporter system.

  3. Data indicate that ataluren (0.1-1 muM, 3-5 dpf) improved contractile function (~60% improvement of force at 0.5 muM) and dystrophin expression.

  4. Ordered disorder of the astrocytic dystrophin-associated protein complex in the norm and pathology.

  5. early expression of the short carboxyl-terminal dystrophin transcript, with expression of the full length muscle transcript occurring during myogenesis.

  6. Data suggest that dystrophin functions in regulation of calcium signaling during early stages of slow muscle cell differentiation; calcium signaling in these cells coincide with first spontaneous contractions of embryonic trunk.

  7. analysis of the dystrophin associated protein complex in zebrafish

  8. Data suggest that the progressive muscle degeneration phenotype of dystrophin mutant zebrafish embryos is caused by the failure of embryonic muscle end attachments.

  9. Dystrophin family gene expression in zebrafish is reported.

  10. reduction of dystrophin, dystroglycan (show DAG1 ELISA Kits) and sarcoglycan (show SGCD ELISA Kits) at translational level in embryos with overexpressed myostatin2

Fruit Fly (Drosophila melanogaster) Dystrophin (DMD) interaction partners

  1. Dys (show DAG1 ELISA Kits) protein regulates tarsal joint formation in response to Notch (show NOTCH1 ELISA Kits) activity during Drosophila leg development.

  2. The findings suggest that the signaling functions of Dystrophin protein are able to ameliorate dilated cardiomyopathy, and thus might help to improve heart muscle function in micro-Dystrophin-based gene therapy approaches.

  3. Nrk (show NRK ELISA Kits), mbl, capt and Cam (show CALM ELISA Kits) genetically interact with dystrophin and/or dystroglycan (show DAG1 ELISA Kits) in the process of axon path-finding in the eye.

  4. only dystroglycan (show DAG1 ELISA Kits), but not dystrophin deficiency causes myodegeneration induced by energetic stress suggesting that dystroglycan (show DAG1 ELISA Kits) might be a component of the low-energy pathway and act as a transducer of energetic stress in normal and dystrophic muscles

  5. Dystrophin and the Rho GTPase (show RACGAP1 ELISA Kits) crossveinless-c signaling pathway likely interact at the postsynaptic side of the NMJ to maintain synaptic homeostasis.

  6. Lack of the large dystrophin isoforms in the postsynaptic muscle cell leads to elevated evoked neurotransmitter release from presynaptic terminals.

  7. Our results indicate the existence of at least two possibly separate roles of dystrophin in muscle, maintaining synaptic homeostasis and preserving the structural stability of the muscle.

  8. The det locus encodes Drosophila dys, which acts with other components of the DAPC to influence intercellular signalling in developing wing veins.

  9. Possibility that Dp186 modulates other non-Gbb/Wit-dependent retrograde signaling pathways required to maintain normal synaptic physiology.

Human Dystrophin (DMD) interaction partners

  1. It concluded that Dp71, comprising Dp71b and Dp71ab, was expressed exclusively in HEK293 cells and that Dp71ab was specifically localized to the nucleus. Our findings suggest that Dp71ab in the nucleus contributes to the diverse functions of HEK293 cells.

  2. This study aimed to provide in vitro quantitative evidence of the ability of human mesoangioblasts to restore dystrophin, in terms of protein accumulation and distribution, within myotubes derived from patients with Duchenne muscular dystrophy.

  3. In TMD patients, a novel locus at genome-wide level of significance (rs73460075, OR = 0.56, P = 3.8 x 10(-8)) in the intron of the dystrophin gene DMD (X chromosome), and a suggestive locus on chromosome 7 (rs73271865, P = 2.9 x 10(-7)) upstream of the Sp4 Transcription Factor ( SP4) gene were identified in the discovery cohort, but neither of these was replicated.

  4. As exon 44 skipping-amenable DMD has a later loss of ambulation, mutation-specific randomization and selection of placebo groups are essential for the success of clinical trials

  5. We focused on four prevalent mutated proteins deleted in RDelta45-47, RDelta45-48, RDelta45-49, and RDelta45-51, analyzing protein/membrane interactions. Mutants RDelta45-48 and RDelta45-51 led to mild pathologies and displayed a similar triple coiled-coil structure as the full-length DYS (show IKBKAP ELISA Kits) R16 (show SLC1A5 ELISA Kits)-21, whereas the two others, RDelta45-47 and RDelta45-49, induced more severe pathologies and showed "fractional" structures unre...

  6. The dystrophin expression plasmids described here will be useful in cell and gene therapy studies aimed at ameliorating Duchenne muscular dystrophy

  7. In Korean boys, 117 different deletions, 48 duplications, and 90 pathogenic sequence variations, including 30 novel variations, were identified. Deletions and duplications accounted for 65.4% and 13.3% of Korean dystrophinopathy, respectively, suggesting that the incidence of large rearrangements in dystrophin is similar among different ethnic groups.

  8. Detected are the expression of endogenous exons 44-56 connected mRNA transcript of the DMD using total RNAs derived from human normal skeletal muscle by reverse transcription polymerase chain reaction and identified are a total of eight types of multiple exon skipping products around the mutation hotspot.

  9. Thus using NGS we have identified a pathogenic DMD mutation from degraded DNA and low-level somatic mosaicism, which would have been overlooked using Sanger sequencing.

  10. Four nonsense, one frameshift and two splice site mutations as well as two missense variants have been found in dystrophin gene in Iranian Duchenne and Becker muscular dystrophy patients.

Pig (Porcine) Dystrophin (DMD) interaction partners

  1. Data indicate that skeletal muscles from with a missense mutation in the dystrophin gene is associated with muscle histophatology.

Mouse (Murine) Dystrophin (DMD) interaction partners

  1. Our study demonstrates for the first time that low-level dystrophin can partially preserve heart function.

  2. Dp71 expression in hepatic cells is carried out, in part, by YY1 (show YY1 ELISA Kits)-, Sp1 (show SP1 ELISA Kits)- and Sp3 (show SP3 ELISA Kits)-mediated transcription from the Dp71 promoter.

  3. Deficit in cognitive flexibility was observed in mdx mice in the absence of motor dysfunction or general learning impairments.

  4. Our data also support the hypothesis that altered spatial localization of GABAA (show GABRg1 ELISA Kits) receptors due to Dp427 loss is a pathological mechanism associated with brain dysfunction in DMD, suggesting that extrasynaptic GABAA (show GABRg1 ELISA Kits) receptors might be candidate targets for future therapeutic developments.

  5. This finding represents the first functional evidence for a significant role of the dystrophin-associated protein complex in the regulation of Kir2.x channels.

  6. Lack of dystrophin in mdx mice appears associated with defective epithelial differentiation

  7. Dp71Delta78-79 dystrophin mutant stimulates neurite outgrowth in cultured neuronal cells via upregulation and phosphorylation of HspB1 (show HSPB1 ELISA Kits).

  8. this study provided evidence that the Dystrophin Dp71, a membrane-associated cytoskeletal protein (show DRP2 ELISA Kits) and the main DMD gene product in the retina, regulates astrocyte morphology and density and is associated with subsequent normal blood vessel development

  9. The novel dystrophin reporter mouse provides a valuable tool for direct visualization of dystrophin expression and will allow the study of dystrophin expression in vivo and in vitro in various tissues by live cell imaging.

  10. Dystrophin-based therapy improves fragility of the dystrophic skeletal muscle by preventing reduction in muscle excitability.

Dystrophin (DMD) Antigen Profile

Antigen Summary

The dystrophin gene is the largest gene found in nature, measuring 2.4 Mb. The gene was identified through a positional cloning approach, targeted at the isolation of the gene responsible for Duchenne (DMD) and Becker (BMD) Muscular Dystrophies. DMD is a recessive, fatal, X-linked disorder occurring at a frequency of about 1 in 3,500 new-born males. BMD is a milder allelic form. In general, DMD patients carry mutations which cause premature translation termination (nonsense or frame shift mutations), while in BMD patients dystrophin is reduced either in molecular weight (derived from in-frame deletions) or in expression level. The dystrophin gene is highly complex, containing at least eight independent, tissue-specific promoters and two polyA-addition sites. Furthermore, dystrophin RNA is differentially spliced, producing a range of different transcripts, encoding a large set of protein isoforms. Dystrophin (as encoded by the Dp427 transcripts) is a large, rod-like cytoskeletal protein which is found at the inner surface of muscle fibers. Dystrophin is part of the dystrophin-glycoprotein complex (DGC), which bridges the inner cytoskeleton (F-actin) and the extra-cellular matrix.

Alternative names and synonyms associated with Dystrophin (DMD)

  • dystrophin (DMD) Elisa Kit
  • dystrophin (Dmd) Elisa Kit
  • dystrophin (dmd) Elisa Kit
  • Dystrophin (Dys) Elisa Kit
  • dystrophin, muscular dystrophy (Dmd) Elisa Kit
  • BMD Elisa Kit
  • cb664 Elisa Kit
  • CG7240 Elisa Kit
  • CG7243 Elisa Kit
  • CG7344 Elisa Kit
  • CG17750 Elisa Kit
  • CG31175 Elisa Kit
  • CG34157 Elisa Kit
  • CMD3B Elisa Kit
  • det Elisa Kit
  • DKFZp459C1629 Elisa Kit
  • DKFZp468A1620 Elisa Kit
  • DLP Elisa Kit
  • DLP1 Elisa Kit
  • DLP2 Elisa Kit
  • DLP3 Elisa Kit
  • DLP186 Elisa Kit
  • dmd Elisa Kit
  • dmDLP Elisa Kit
  • dmDp186 Elisa Kit
  • dmDys Elisa Kit
  • Dmel\\CG34157 Elisa Kit
  • DNADMD1 Elisa Kit
  • Dp71 Elisa Kit
  • Dp117 Elisa Kit
  • Dp186 Elisa Kit
  • Dp205 Elisa Kit
  • Dp427 Elisa Kit
  • DXS142 Elisa Kit
  • DXS164 Elisa Kit
  • DXS206 Elisa Kit
  • DXS230 Elisa Kit
  • DXS239 Elisa Kit
  • DXS268 Elisa Kit
  • DXS269 Elisa Kit
  • DXS270 Elisa Kit
  • DXS272 Elisa Kit
  • DXSmh7 Elisa Kit
  • DXSmh9 Elisa Kit
  • dys Elisa Kit
  • GI3046716 Elisa Kit
  • IDLP Elisa Kit
  • im:6911785 Elisa Kit
  • mdx Elisa Kit
  • MGC79631 Elisa Kit
  • MGC83347 Elisa Kit
  • pke Elisa Kit
  • RATDMD Elisa Kit
  • zfDYS Elisa Kit
  • zgc:110165 Elisa Kit

Protein level used designations for Dystrophin (DMD) ELISA Kits

dystrophin , Duchenne muscular dystrophy , dystrophin isoform Dp116 , sap , sapje , CG34157-PA , CG34157-PB , CG34157-PC , CG34157-PD , CG34157-PE , CG34157-PF , CG34157-PG , CG34157-PH , CG34157-PI , CG34157-PJ , CG34157-PK , CG34157-PL , Dys-PA , Dys-PB , Dys-PC , Dys-PD , Dys-PE , Dys-PF , Dys-PG , Dys-PH , Dys-PI , Dys-PJ , Dys-PK , Dys-PL , Dystrophin-like protein 1 , Dystrophin-like protein 186 , Dystrophin-like protein 2 , Dystrophin-like protein 3 , detached , dystrophin Dp186 , dystrophin (muscular dystrophy, Duchenne and Becker types) , dystrophin Dp71 isoform , RNDNADMD1 , apodystrophin-3 , apodystrophin-I , dystrophin transcript variant Dp71e , dystrophin, muscular dystrophy , X-linked muscular dystrophy

100051515 Equus caballus
708073 Macaca mulatta
399334 Xenopus laevis
100172693 Pongo abelii
465557 Pan troglodytes
493417 Xenopus (Silurana) tropicalis
100174396 Pongo abelii
100329118 Xenopus (Silurana) tropicalis
449606 Pan troglodytes
445738 Ciona intestinalis
83773 Danio rerio
42327 Drosophila melanogaster
100406331 Callithrix jacchus
1756 Homo sapiens
606758 Canis lupus familiaris
24907 Rattus norvegicus
396236 Gallus gallus
100727002 Cavia porcellus
497636 Sus scrofa
540755 Bos taurus
101119444 Ovis aries
13405 Mus musculus
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