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Recombinant Human DAG1 Protein, His-tagged

Cat.No. : DAG1-620H
Product Overview : Recombinant human DAG1 (NP_004384.4) (Met1-Val749) was expressed with a polyhistidine tag at the C-terminus.
  • Specification
  • Gene Information
  • Related Products
Source : HEK293
Species : Human
Tag : His
Predicted N Terminal : His 30
Form : Lyophilized from sterile PBS, pH 7.4, 5% ~ 8% trehalose and mannitol.
Molecular Mass : The recombinant human DAG1 consists 731 amino acids and predicts a molecular mass of 79.7 kDa.
Endotoxin : < 1.0 EU per μg of the protein as determined by the LAL method.
Purity : >(27.7+42+29) % as determined by SDS-PAGE.
Stability : Samples are stable for up to twelve months from date of receipt at -70ºC.
Storage : Store it under sterile conditions at -20ºC~-70ºC. It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles.
Reconstitution : It is recommended that sterile water be added to the vial to prepare a stock solution of 0.25 ug/ul. Centrifuge the vial at 4℃ before opening to recover the entire contents.
Gene Name : DAG1 dystroglycan 1 (dystrophin-associated glycoprotein 1) [ Homo sapiens ]
Official Symbol : DAG1
Synonyms : DAG1; dystroglycan 1 (dystrophin-associated glycoprotein 1); dystroglycan; 156DAG; A3a; AGRNR; alpha dystroglycan; beta dystroglycan; DAG; dystrophin associated glycoprotein 1; MDDGC7; FLJ51254;
Gene ID : 1605
mRNA Refseq : NM_001165928
Protein Refseq : NP_001159400
MIM : 128239
UniProt ID : Q14118
Chromosome Location : 3p21
Pathway : Arrhythmogenic right ventricular cardiomyopathy (ARVC), organism-specific biosystem; Arrhythmogenic right ventricular cardiomyopathy (ARVC), conserved biosystem; Dilated cardiomyopathy, organism-specific biosystem; Dilated cardiomyopathy, conserved biosystem; ECM-receptor interaction, organism-specific biosystem; ECM-receptor interaction, conserved biosystem; Hypertrophic cardiomyopathy (HCM), organism-specific biosystem;

For Research Use Only. Not intended for any clinical use. No products from Creative BioMart may be resold, modified for resale or used to manufacture commercial products without prior written approval from Creative BioMart.

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Q&As (5)

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Are there any specific animal models used to study DAG1-related muscle disorders? 03/30/2023

Yes, mouse models with mutations in the DAG1 gene are commonly used to study the pathophysiology of DAG1-related muscle disorders.

What are the symptoms of DAG1-related muscle disorders? 01/06/2023

Symptoms can include muscle weakness, hypotonia, and developmental delay, as well as eye and brain abnormalities in some cases.

How does DAG1 protein contribute to the stability of muscle cell membranes? 05/02/2022

DAG1 protein forms a complex with other proteins and glycoproteins to anchor the muscle cell membrane to the extracellular matrix.

Can DAG1 protein be used as a biomarker for muscle disorders? 03/13/2022

Studies are exploring the potential use of DAG1 protein levels as a diagnostic and prognostic biomarker for muscle disorders.

How does DAG1 protein interact with other proteins in the muscle cell membrane? 09/07/2017

DAG1 protein forms a complex with dystrophin, sarcoglycans, and other proteins to maintain the stability of the muscle cell membrane.

Customer Reviews (3)

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Reviews
08/17/2022

    By utilizing the DAG1 protein in my experiments, I can trust that I am working with a product of the highest caliber, backed by a company dedicated to delivering exceptional quality and support.

    01/23/2022

      The reliability and reproducibility of the DAG1 Protein's performance make it a go-to option for WB experiments.

      03/12/2021

        The DAG1 protein is of exceptional quality and will undoubtedly meet my experimental needs with utmost reliability and accuracy.

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