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Description_x000D_
General description_x000D_
PYGM catalyzes and regulates the breakdown of glycogen to glucose-1-phosphate. Defects in PYGM are the cause of glycogen storage disease type 5 (GSD5), also known as McArdle disease. GSD5 is a metabolic disorder resulting in myopathy characterized by exercise intolerance, cramps, muscle weakness and recurrent myoglobinuria._x000D_
Immunogen_x000D_
PYGM (NP_005600, 522-556)_x000D_
This antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide selected from the center region of human PYGM._x000D_
Physical form_x000D_
Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide.
- Related Categories Alphabetical Index, Antibodies, PT-PY, Primary Antibodies conjugate