Catalog No.
YHC89501
Expression system
E. coli
Species
Homo sapiens (Human)
Protein length
Ser3066-Ile3321
Predicted molecular weight
31.64 kDa
Nature
Recombinant
Endotoxin level
Please contact with the lab for this information.
Purity
>90% as determined by SDS-PAGE.
Accession
P11532
Applications
ELISA, Immunogen, SDS-PAGE, WB, Bioactivity testing in progress
Form
Lyophilized
Storage buffer
Lyophilized from a solution in PBS pH 7.4, 0.02% NLS, 1mM EDTA, 4% Trehalose, 1% Mannitol.
Reconstitution
Reconstitute in sterile water for a stock solution. A copy of datasheet will be provided with the products, please refer to it for details.
Shipping
In general, proteins are provided as lyophilized powder/frozen liquid. They are shipped out with dry ice/blue ice unless customers require otherwise.
Stability and Storage
Use a manual defrost freezer and avoid repeated freeze thaw cycles. Store at 2 to 8°C for frequent use. Store at -20 to -80°C for twelve months from the date of receipt.
Alternative Names
DMD, Dystrophin
The Glycine-Rich Region as a Flexible Molecular Glue Promoting hPrP106-145 Aggregation into β-Sheet Structures., PMID:40509809
Early endosome disturbance and endolysosomal pathway dysfunction in Duchenne muscular dystrophy., PMID:40499778
Expression of full-length dystrophin reverses muscular dystrophy defects in young and old mdx4cv mice., PMID:40493400
Extensive striated muscle damage in a rat model of Duchenne muscular dystrophy with Dmd exons 10-17 duplication., PMID:40490752
Protocol for using MYOD1-transduced human urine-derived cells as a predictive platform for exon skipping therapy in Duchenne muscular dystrophy., PMID:40483693
Contrasting Becker and Duchenne muscular dystrophy serum biomarker candidates by using data independent acquisition LC-MS/MS., PMID:40483507
GYY4137, a Slow-Releasing Hydrogen Sulfide Donor, Attenuates Skeletal Muscle Abnormalities in a Murine Model of Duchenne Muscular Dystrophy., PMID:40476490
Muscle stem cells in Duchenne muscular dystrophy exhibit molecular impairments and altered cell fate trajectories impacting regenerative capacity., PMID:40473604
Periostin Exon 17 Skipping Enhances the Efficacy of Local Adeno-Associated Viral-Microdystrophin Administration in a Fibrotic Model of Duchenne Muscular Dystrophy., PMID:40462744
L-glutamine- and enzyme-supplementation via liquid feed to suckling piglets does not impact growth, health or intestinal structure., PMID:40453319
Comparison between endovascular and surgical treatment of acute arterial occlusive mesenteric ischemia., PMID:40452055
Neuronal hyperexcitability in dystrophin-deficient mdx hippocampal neurons: the importance of interleukin-6 and GABAergic regulation., PMID:40447687
The promoting effect of high-fat diet-induced trained immunity on ulcerative colitis and the mechanism of the therapeutic effect of Dahuang Mudan Decoction., PMID:40446577
Serum protein biomarker signature of Duchenne muscular dystrophy., PMID:40438995
Systemic mRNA Delivery into the Muscle of Duchenne Muscular Dystrophy Model Mice Using Alpha-Dystroglycan Binding Peptide Modified Lipid Nanoparticles., PMID:40436778
Dux Is Dispensable for Skeletal Muscle Regeneration: A Study Inspired by a "Red Flagged" Publication and Editorial Oversight., PMID:40422198
An engineered U7 small nuclear RNA scaffold greatly increases ADAR-mediated programmable RNA base editing., PMID:40419487
A comprehensive spatiotemporal map of dystrophin isoform expression in the developing and adult human brain., PMID:40400011
Pilot study of canakinumab (Ilaris) in steroid naïve children with Duchenne muscular dystrophy demonstrates safety and exploratory changes in potential serum protein response biomarkers., PMID:40396427
Diffuse Active Myocarditis in a Teenager with Duchenne Muscular Dystrophy - a case report., PMID:40389882
Network analysis of the cerebrospinal fluid proteome reveals shared and unique differences between sporadic and familial forms of amyotrophic lateral sclerosis., PMID:40375307
DG9 boosts PMO nuclear uptake and exon skipping to restore dystrophic muscle and cardiac function., PMID:40368879
CRISPR/Cas9 Ribonucleoprotein Delivery Enhanced by Lipo-Xenopeptide Carriers and Homology-Directed Repair Modulators: Insights from Reporter Cell Lines., PMID:40362595
GsMTx4-blocked PIEZO1 channel promotes myogenic differentiation and alleviates myofiber damage in Duchenne muscular dystrophy., PMID:40361216
Identification of VDAC1 as a mitochondria-related target of Duchenne muscular dystrophy based on bioinformatics analysis and in vitro experiments., PMID:40359883
Template-assisted sequence knockin rescues skeletal and cardiac muscle function in a deletion model of Duchenne muscular dystrophy., PMID:40340246
Advances in Duchenne Muscular Dystrophy: Diagnostic Techniques and Dystrophin Domain Insights., PMID:40332074
Plasma Microvesicles May Contribute to Muscle Damage in the mdx Mouse Model of Duchenne Muscular Dystrophy., PMID:40331939
Label-free Detection of Urine Extracellular Vesicles from Duchenne Muscular Dystrophy Patients Using Surface-Enhanced Raman Spectroscopy Combined with Machine Learning Models., PMID:40321535
Clinical applications of exon-skipping antisense oligonucleotides in neuromuscular diseases., PMID:40308063
Exercise combined with corticoid/omega-3 therapy positively affected skeletal and cardiac muscles in middle aged mdx mice., PMID:40308028
LncRNA-MEG3 Regulates Muscle Mass and Metabolic Homeostasis by Facilitating SUZ12 Liquid-Liquid Phase Separation., PMID:40285575
Use of an In Vitro Digestibility Approach to Assess Bombyx mori and Camelina sativa as Alternative Feed Ingredients for Poultry Species., PMID:40267002
Oestrogen Receptor Alpha in Myocyte Maintains Muscle Regeneration in Duchenne Muscular Dystrophy., PMID:40258782
Contribution of Japanese scientists to drug metabolism and disposition., PMID:40245580
Optimized efficient screening for Duchenne muscular dystrophy carriers using proto-oncogene tyrosine-protein kinase receptor Ret., PMID:40244132
Gene Editing for Duchenne Muscular Dystrophy: From Experimental Models to Emerging Therapies., PMID:40241992
Nuclear Deformation and Stiffness-Dependent Traction Force Generation Dictate the Migration of Cells under Confinement., PMID:40230252
Grain Type Impacts Feed Intake, Milk Production and Body Temperature of Dairy Cows Exposed to an Acute Heat Event in Early Lactation., PMID:40218438
Strategy for drug repurposing in fibroadipogenic replacement during muscle wasting: application to duchenne muscular dystrophy., PMID:40206397
Mechanisms of cardiomyopathy in duchenne muscular dystrophy: A study using pluripotent stem cells derived from patients with severe and mild motor impairment., PMID:40203679
The SIRT1 activator SRT2104 exerts exercise mimetic effects and promotes Duchenne muscular dystrophy recovery., PMID:40195304
Volitional exercise elicits physiological and molecular improvements in the severe D2.mdx mouse model of Duchenne muscular dystrophy., PMID:40189894
AOC 1044 induces exon 44 skipping and restores dystrophin protein in preclinical models of Duchenne muscular dystrophy., PMID:40183632
The road toward AAV-mediated gene therapy of Duchenne muscular dystrophy., PMID:40181545
Evaluation of forage yield and nutritive value of lesser burnet genotypes., PMID:40175420
Solid state fermentation: A strategy for wheat bran supplemented corn stover valorization with Pleurotus species., PMID:40161241
Duchenne muscular dystrophy gene product expression is associated with survival in head and neck squamous cell carcinoma., PMID:40155657
Single-cut gene therapy in a one-step generated rhesus monkey model of Duchenne muscular dystrophy., PMID:40147446
Valproic Acid Improves Antisense-Mediated Exon-Skipping Efficacy in mdx Mice., PMID:40141224
For research use only. Not for human or drug use.
