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Conditions of optimal PYGL Enzyme performance should be determined experimentally by the investigator.
Price/availability/specifications subject to change without notice. Unless otherwise indicated, our catalog and customized products are for research use only and not intended for human or animal diagnostic or therapeutic use.
Phone: 1-617-401-8149
Fax: 1-617-606-5019
Email: message@sydlabs.com
Or leave a message with a formal purchase
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Introduction
Glycogen phosphorylase, liver form (PYGL) belongs to the glycogen phosphorylase family. All known phosphorylases have the same catalytic and structural properties. But enzymes from different sources different in their regulatory mechanisms and natural substrates. Glycogen phosphorylase catalyzes the rate-limiting step in glycogenolysis in animals by releasing glucose-1-phosphate from the terminal alpha-1,4-glycosidic bond. Glycogen phosphorylase exists as a homodimer which associate into a tetramer to form the enzymatically active phosphorylase A. Defects in PYGL would cause the glycogen storage disease type 6 (GSD6). It is a metabolic disorder disease, characterized by mild to moderate hypoglycemia, prominent hepatomegaly and growth retardation.
BP001424-C976: Recombinant Human Glycogen phosphorylase, liver form
Source: HEK 293-derived.
Purity > 95%, by reducing SDS-PAGE.
Endotoxin: Less than 0.1 ng/ug (1 EU/ug).
Shipping: The product is shipped at ambient temperature. Upon receipt, store it immediately at the temperature recommended below.
Stability & Storage: Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
12 months from date of receipt, -20 to -?0C as supplied.
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