Analytical Data
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Gene name
DMWD
- Application
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Alternative Names
D19S593E; DM 9; DM9; DMR N9; DMR N9 protein; DMRN 9; DMRN9; DMWD; DMWD_HUMAN; Dystrophia myotonica containing WD repeat motif; Dystrophia myotonica containing WD repeat motif protein; Dystrophia myotonica WD repeat containing protein; Dystrophia myotonica WD repeat-containing protein
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Species
Human
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Source
E. coli
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Tag
GST-tag at N-terminal
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Purity
Greater than 90% as determined by SDS-PAGE.
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Uniprot
Q09019
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Expression Region
1-334aa
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AA Sequence
MLLRGLMKSYFGGLLCVCWSPDGRYVVTGGEDDLVTVWSFTEGRVVARGHGHKSWVNAVAFDPYTTRAEEAATAAGADGERSGEEEEEEPEAAGTGSAGGAPLSPLPKAGSITYRFGSAGQDTQFCLWDLTEDVLYPHPPLARTRTLPGTPGTTPPAASSSRGGEPGPGPLPRSLSRSNSLPHPAGGGKAGGPGVAAEPGTPFSIGRFATLTLQERRDRGAEKEHKRYHSLGNISRGGSGGSGSGGEKPSGPVPRSRLDPAKVLGTALCPRIHEVPLLEPLVCKKIAQERLTVLLFLEDCIITACQEGLICTWARPGKAGISSQPGNSPSGTVV
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Molecular Weight
62.37 kDa
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Endotoxin
< 1.0 EU per μg protein as determined by the LAL method.
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Form
Freeze-dried powder
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Buffer formulation
PBS, pH7.4, containing 0.01% SKL, 1mM DTT, 5% Trehalose and Proclin300.
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Reconstitution
Reconstitute in ddH2O to a concentration of 0.1-0.5 mg/mL. Do not vortex.
- Customization
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Stability Test
The thermal stability is described by the loss rate. The loss rate was determined by accelerated thermal degradation test, that is, incubate the protein at 37℃ for 48h, and no obvious degradation and precipitation were observed. The loss rate isless than 8% within the expiration date under appropriate storage condition.
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Storage & Shelf Life
Samples are stable for up to twelve months from date of receipt at -20℃ to -80℃. Store it under sterile conditions at -20℃ to -80℃. It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles.
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Shipping
In general, recombinant proteins are supplied as lyophilized powder and shipped at ambient temperature. For bulk packages, the proteins are provided as frozen liquid and shipped with blue ice, unless otherwise requested by the customer.
Quality inspection process
Related Products
Protein Description
The study of DMWD (Duchenne muscular dystrophy-associated protein) recombinant proteins is rooted in understanding muscular dystrophies, particularly Duchenne muscular dystrophy (DMD), a severe genetic disorder characterized by progressive muscle degeneration. DMD results from mutations in the dystrophin gene, leading to the absence of dystrophin, a crucial protein that stabilizes muscle cell membranes. Research has highlighted the potential therapeutic role of DMWD, which is involved in muscle repair and regeneration. The production of DMWD recombinant proteins enables scientists to investigate their biological functions and interactions within muscle tissues more thoroughly. By exploring how DMWD operates at the molecular level, researchers aim to develop targeted therapies that can restore or enhance its function in DMD patients, potentially mitigating the severe muscle wasting associated with the disease. This line of research is fundamental not only for its implications in treating DMD but also for understanding broader muscle pathology and regeneration mechanisms, paving the way for advanced treatments for various muscle-related disorders.
