Glycogen Synthase 2 Protein (Myc-DYKDDDDK Tag)
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- Antigène Voir toutes Glycogen Synthase 2 (GYS2) Protéines
- Glycogen Synthase 2 (GYS2) (Glycogen Synthase 2, Liver (GYS2))
- Type de proteíne
- Recombinant
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Origine
- Humain
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Source
- HEK-293 Cells
- Purification/Conjugué
- Cette Glycogen Synthase 2 protéine est marqué à la Myc-DYKDDDDK Tag.
- Application
- Antibody Production (AbP), Standard (STD)
- Attributs du produit
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- Recombinant human GYS2 protein expressed in HEK293 cells.
- Produced with end-sequenced ORF clone
- Pureté
- > 80 % as determined by SDS-PAGE and Coomassie blue staining
- Top Product
- Discover our top product GYS2 Protéine
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- Indications d'application
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Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays - Commentaires
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The tag is located at the C-terminal.
- Restrictions
- For Research Use only
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- Concentration
- 50 μg/mL
- Buffer
- 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
- Stock
- -80 °C
- Stockage commentaire
- Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
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- Antigène
- Glycogen Synthase 2 (GYS2) (Glycogen Synthase 2, Liver (GYS2))
- Autre désignation
- Gys2 (GYS2 Produits)
- Synonymes
- cb765 Protein, zgc:112057 Protein, BC021322 Protein, LGS Protein, GLYSN Protein, glycogen synthase 2 Protein, gys2 Protein, Gys2 Protein, GYS2 Protein
- Sujet
- The protein encoded by this gene, liver glycogen synthase, catalyzes the rate-limiting step in the synthesis of glycogen - the transfer of a glucose molecule from UDP-glucose to a terminal branch of the glycogen molecule. Mutations in this gene cause glycogen storage disease type 0 (GSD-0) - a rare type of early childhood fasting hypoglycemia with decreased liver glycogen content.
- Poids moléculaire
- 80.8 kDa
- NCBI Accession
- NP_068776
- Pathways
- AMPK Signaling, Cellular Glucan Metabolic Process
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