Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
This gene encodes a muscle enzyme involved in glycogenolysis. Highly similar enzymes encoded by different genes are found in liver and brain. Mutations in this gene are associated with McArdle disease (myophosphorylase deficiency), a glycogen storage disease of muscle. Alternative splicing results in multiple transcript variants.
AI115133; glycogen muscle; glycogen phosphorylase; glycogen phosphorylase, muscle associated; glycogen phosphorylase, muscle form; GPMM; muscle (McArdle syndrome); muscle glycogen phosphorylase; Muscpho; Myophosphorylase; PG; Phosphorylase glycogen; phosphorylase, glycogen, muscle; Phosphorylase, glycogen; muscle (McArdle syndrome); Pygm; unnamed protein product
100 µL
150 µL
100 µL
100 µg
100 µL
100 µL
50 µg
50 µg
100 µL
100 µg
100 µg
100 µg
100 µg
100 µg
10 mg
1 mL
1 mg
100 µL
Searching for an antibody we don't offer? We make custom antibodies for specific targets, species and applications.
More than 18,000 custom antibodies created so far.
Talk to a specialist nowIf an Invitrogen™ antibody doesn't perform as described on our website or datasheet,we'll replace the product at no cost to you, or provide you with a credit for a future purchase.*
Learn moreGet expert recommendations for common problems or connect directly with an on staff expert for technical assistance related to applications, equipment and general product use.
Contact tech support