PYGM monoclonal Antibody | MB64781

PYGM monoclonal Antibody | MB64781 | Gentaur UK, US & Europe Distribution

Host: Mouse

Reactivity: Human, Mouse, Rat

Application: IHC, WB

Application Range: WB 1:2000, IHC 1:2000

Background: 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. [provided by RefSeq, Sep 2009]

Storage & Stability: PBS (PH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide.

Specificity: phosphorylase, glycogen, muscle

Molecular Weight: 96.9 kDa (Predicted)

Note: For research use only, not for use in diagnostic procedure.

Alternative Names: glycogen; glycogen phosphorylase; glycogen storage disease type V; glycogen storage disease type V) ; McArdle syndrome; muscle; muscle (McArdle syndrome; myophosphorylase; phosphorylase

Immunogen: Human recombinant protein fragment corresponding to amino acids 698-842 of human PYGM (NP_005600) produced in E.coli.

Conjugate: Unconjugated

Modification: Unmodification

Purification & Purity: Purified from mouse ascites fluids or tissue culture supernatant by affinity chromatography (protein A/G)

Pathway: N/A