GYS1 Protein, Human (His)

Glycogen synthase (GYS1) facilitates the transfer of a glycosyl residue from UDP-Glc to alpha-1,4-glucan, a vital step in glycogen synthesis. GYS1's enzymatic activity sequentially adds glucose residues to the growing glycogen chain, regulating cellular glycogen levels and contributing to energy storage and metabolism. GYS1 Protein, Human (His) is the recombinant human-derived GYS1 protein, expressed by E. coli, with C-His labeled tag.

Glycogen synthase (GYS1) is an enzyme responsible for the transfer of a glycosyl residue from UDP-Glc to the non-reducing end of alpha-1,4-glucan. This enzymatic activity is crucial in the process of glycogen synthesis, where glucose residues are sequentially added to the growing glycogen chain. GYS1 plays a central role in regulating glycogen levels within cells, contributing to energy storage and metabolism.

Human

E. coli

C-His

P13807-1 (M1-N737)

2997

Full Length of Isoform-1

Approximately 70-80 kDa,based on SDS-PAGE under reducing conditions.

Greater than 85% as determined by reducing SDS-PAGE.

Solution

Supplied as 0.22 μm filtered solution in 20 mM Tris, 0.5 M NaCl, 0.5 M Arginine, pH8.0 with glycerol as protectant.
Note: For SPR assay, please replace the buffer. Primary amine components (e.g., Tris, imidazole) can affect protein-coupled chips.

<1 EU/μg, determined by LAL method.

N/A.

Stored at -80°C for 1 year from date of receipt. It is stable at -20°C for 3 months after opening. It is recommended to freeze aliquots at -80°C for extended storage. Avoid repeated freeze-thaw cycles.

Shipping with dry ice.