Anti-Human/Mouse/Rat PYGM Polyclonal Antibody

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.
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Properties

Data Sheet Click for Datasheet
Catalog Number PA10319
Size 100μl
Host Type Rabbit
Immunogen Recombinant protein of human PYGM
Specificity
Isotype IgG
Reacitivity Human,Mouse,Rat
Clone
Uniprot P11217
Concentration 0.3 mg/mL
Dilution WB 1:200-1:1000
Formulation
Application WB,ELISA
Other Names Glycogen phosphorylase,Glycogen phosphorylase muscle form,muscle form,Muscpho,Myophosphorylase,Phosphorylase glycogen muscle (McArdle syndrome glycogen storage disease type V),Pygm,PYGM
Storage Lyophilized product: 5 years at 2 - 8°C; Solution: 2 years at -20°C.
Postscript For research use only, not for use in diagnostic procedures.

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