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anti-Utrophin (UTRN) Antibodies

UTRN shares both structural and functional similarities with the dystrophin gene. Additionally we are shipping Utrophin Kits (15) and and many more products for this protein.

list all antibodies Gene Name GeneID UniProt
UTRN 7402 P46939
Anti-Rat UTRN UTRN 25600  
UTRN 22288  
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Top anti-Utrophin Antibodies at

Showing 7 out of 8 products:

Catalog No. Reactivity Host Conjugate Application Images Quantity Supplier Delivery Price Details
Mouse Mouse Un-conjugated IF, WB Western blot analysis of Utrophin on a mouse neonate lysate. Lane 1: 1: 250, lane 2: 1: 500, lane 3: 1:1000 dilution of the mouse anti-mouse Utrophin antibody. 50 μg Log in to see 5 to 6 Days
Human Mouse Un-conjugated IF, ELISA, WB Immunofluorescence of monoclonal antibody to UTRN on HeLa cell. [antibody concentration 10 ug/ml] Detection limit for recombinant GST tagged UTRN is 0.1 ng/ml as a capture antibody. 100 μg Log in to see 9 Days
Human Mouse Un-conjugated ELISA, WB Western Blot detection against Immunogen (37.77 KDa) . 50 μL Log in to see 9 Days
Human Mouse Un-conjugated IF, ELISA, WB   100 μg Log in to see 8 to 10 Days
Human Rabbit Un-conjugated ICC, IF, IHC, IHC (p)   25 μL Log in to see 8 to 11 Days
Human Mouse Un-conjugated IF, ELISA, WB   100 μg Log in to see 11 to 16 Days
Human Rabbit Un-conjugated   100 μg Log in to see 69 Days

UTRN Antibodies by Reactivity, Application, Clonality and Conjugate

Attributes Applications Host Clonality
Human ,
Mouse (Murine)

Top referenced anti-Utrophin Antibodies

  1. Mouse (Murine) Monoclonal Utrophin Primary Antibody for IF, WB - ABIN968237 : Deconinck, Rafael, Skinner, Brown, Potter, Metzinger, Watt, Dickson, Tinsley, Davies: Utrophin-dystrophin-deficient mice as a model for Duchenne muscular dystrophy. in Cell 1997 (PubMed)
    Show all 5 references for ABIN968237

More Antibodies against Utrophin Interaction Partners

Zebrafish Utrophin (UTRN) interaction partners

  1. utrophin gene expression was dominated by the full length transcript throughout embryogenesis.

Human Utrophin (UTRN) interaction partners

  1. Correlation of Utrophin Levels with the Dystrophin (show DMD Antibodies) Protein Complex and Muscle Fibre Regeneration in Duchenne and Becker Muscular Dystrophy Muscle Biopsies.

  2. there is an inverse correlation between the level of muscle fibrosis and the level of utrophin and that of the number of revertant myofibers in Duchenne muscular dystrophy (show DMD Antibodies)

  3. probed the role of N-terminal CH1 and C-terminal CH2 (show Acyp1 Antibodies) domains in the structure and function of dystrophin (show DMD Antibodies) tandem CH domain and compared with earlier results on utrophin to understand the unifying principles of how tandem CH domains work

  4. targeting Drp1 (show CRMP1 Antibodies)-dependent mitochondrial dynamics may provide a novel strategy to suppress breast cancer metastasis and improve the chemotherapeutic effect in the future

  5. The actin binding affinity of the utrophin tandem calponin-homology domain (CH) is determined by its CH1 domain, when compared to its CH2 (show Acyp1 Antibodies) domain.

  6. this study demonstrated a pathway for Drp1 (show CRMP1 Antibodies) autophagic degradation. Chemical inhibition of lysosomal degradation and ATG7 (show ATG7 Antibodies) knockdown increased Drp1 (show CRMP1 Antibodies) levels.

  7. UtroUp recognises 18 base pairs of the utrophin promoter and efficiently drives utrophin upregulation.

  8. This family study showed that the 6q24.2 mircoduplication of the utrophin gene is a potential risk factor for the development of annular pancreas.

  9. The present findings demonstrate that genotoxic stress in neurons results in p53 (show TP53 Antibodies)-dependent declines in Drp1 (show CRMP1 Antibodies) and parkin (show PARK2 Antibodies) levels contribute to altered mitochondrial morphology and cell death.

  10. UAPC located in caveolae and non-caveolae lipid raft domains of HUVECs may have a mechanosensory function that could participate in the control of eNOS (show NOS3 Antibodies) activity

Mouse (Murine) Utrophin (UTRN) interaction partners

  1. Results support the hypothesis that utrophin is not involved in extraocular muscle sparing in mdx:utrophin(+/-) and mdx:utrophin(-/-) mice

  2. Correlation of Utrophin Levels with the Dystrophin (show DMD Antibodies) Protein Complex and Muscle Fibre Regeneration in Duchenne and Becker Muscular Dystrophy Muscle Biopsies.

  3. This detailed evaluation of the SMT C1100 drug series strongly endorses the therapeutic potential of utrophin modulation as a disease modifying therapeutic strategy for all Duchenne muscular dystrophy (show DMD Antibodies) patients irrespective of their dystrophin (show DMD Antibodies) mutation.

  4. cap-independent mode has significant contribution as cap-dependent translation is severely repressed with utrophin-A 5'-UTR (show UTS2R Antibodies)

  5. Utrophin suppresses low frequency oscillations and coupled gating of mechanosensitive ion channels in dystrophic skeletal muscle

  6. Sarcospan (show SSPN Antibodies)-mediated amelioration of muscular dystrophy in mouse model is dependent on the presence of both utrophin and alpha7beta1 integrin

  7. Results showed that mdx (show DMD Antibodies)/utrn+/- mouse develops fibrosis in both hind limb and respiratory skeletal muscles at a young age while not being so affected such that it dies prematurely, this model may be an appropriate for Duchenne muscular dystrophy (show DMD Antibodies).

  8. 5-amino-4-imidazolecarboxamide riboside treatment increases utrophin A and beta-dystroglycan expression in mdx (show DMD Antibodies) mouse muscle.

  9. utrophin depletion in dystrophin (show DMD Antibodies)-deficient mdx (show DMD Antibodies) muscle affects gating of mechanosensitive ion channels.

  10. Dystrophin (show DMD Antibodies) binds microtubules with high affinity and pauses microtubule polymerization, whereas utrophin does not.

Utrophin (UTRN) Antigen Profile

Protein Summary

This gene shares both structural and functional similarities with the dystrophin gene. It contains an actin-binding N-terminus, a triple coiled-coil repeat central region, and a C-terminus that consists of protein-protein interaction motifs which interact with dystroglycan protein components. The protein encoded by this gene is located at the neuromuscular synapse and myotendinous junctions, where it participates in post-synaptic membrane maintenance and acetylcholine receptor clustering. Mouse studies suggest that this gene may serve as a functional substitute for the dystrophin gene and therefore, may serve as a potential therapeutic alternative to muscular dystrophy which is caused by mutations in the dystrophin gene. Alternative splicing of the utrophin gene has been described\; however, the full-length nature of these variants has not yet been determined.

Gene names and symbols associated with anti-Utrophin (UTRN) Antibodies

  • utrophin (utrn) antibody
  • utrophin (UTRN) antibody
  • utrophin (LOAG_03796) antibody
  • utrophin (Utrn) antibody
  • utrophin (LOC100351667) antibody
  • AA589569 antibody
  • DKFZp469A0710 antibody
  • Dmdl antibody
  • DRP antibody
  • DRP1 antibody

Protein level used designations for anti-Utrophin (UTRN) Antibodies

utrophin , utrophin, or dystrophin-related protein 1 , DRP-1 , dystrophin-related protein 1 , utrophin (homologous to dystrophin) , G-utrophin , urotrophin

398351 Xenopus laevis
463046 Pan troglodytes
9941190 Loa loa
100034367 Danio rerio
100172525 Pongo abelii
100489198 Xenopus (Silurana) tropicalis
100409599 Callithrix jacchus
100551145 Meleagris gallopavo
100552503 Anolis carolinensis
100590343 Nomascus leucogenys
7402 Homo sapiens
25600 Rattus norvegicus
22288 Mus musculus
421610 Gallus gallus
442965 Canis lupus familiaris
100523292 Sus scrofa
534358 Bos taurus
100351667 Oryctolagus cuniculus
100731640 Cavia porcellus
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