PYGM Mouse Monoclonal Antibody [Clone ID: LBI5D1]

• 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]

• Synonyms:

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

• Gene Name:

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

• Gene ID:

  5837

• UniProt:

  P11217

• Conjugation:

  Unconjugated

• Related Pathways:

  Insulin signaling pathway, Starch and sucrose metabolism

• Field of Research:

  Insulin signaling pathway, Starch and sucrose metabolism

• Dilution:

  WB 1:500~2000, IHC 1:2000

• Form:

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

• Buffer:

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

• Function:

  Druggable Genome

• Storage Conditions:

  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.

• Symbol:

  PYGM

• Overview:

  Carrier-free (BSA/glycerol-free) PYGM mouse monoclonal antibody, clone LBI5D1

• Gene ID URL:

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

• Uniprot URL:

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