Synonyms: Anti-Glycogen phosphorylase; Anti-Muscle form; Anti-Myophosphorylase; Anti-PYGM
Storage: -20C
UNSPSC Code: 12352203
Biochem/physiol Actions: 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.
Immunogen: PYGM (NP_005600, 703-737)This antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide selected from the C-terminal region of human PYGM.
Physical form: Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide.
RIDADR: NONH for all modes of transport
WGK Germany: nwg