PYGM Mouse Monoclonal Antibody [Kloon ID: LBI3F9]

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]

Carrier-free (BSA/glycerol-free) PYGM mouse monoclonal antibody, clone LBI3F9

Glycogen; glycogen phosphorylase; glycogen storage disease type V; glycogen storage disease type V) ; McArdle syndrome; muscle; muscle (McArdle syndrome; myophosphorylase; phosphorylase

Homo sapiens glycogen phosphorylase, muscle associated (PYGM), transcript variant 1, mRNA.

5837

P11217

Unconjugated

Insulin signaling pathway, Starch and sucrose metabolism

Insulin signaling pathway, Starch and sucrose metabolism

WB 1:2000, IHC 1:2000

Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)

Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)

Druggable Genome

Stable for 1 year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. Aliquot will be stable at 4°C short term. For long-term storage, aliquot and store at -20°C or below. Stable for 12 months at -20°C. Avoid repeated freeze-thaw cycles.

PYGM

https://www.ncbi.nlm.nih.gov/gene/?term=5837

https://www.uniprot.org/uniprot/P11217