Non disponible en dehors du Royaume-Uni et de l'Irlande
General description
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, 522-556)This antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide selected from the center region of human PYGM.
Physical form
Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide.
Ce produit répond aux critères suivants pour être admissible aux récompenses suivantes :