PYGM Mouse Monoclonal Antibody [Clone ID: LBI5D1]
Product Specifications
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]
Overview
PYGM mouse monoclonal antibody, clone LBI5D1
Synonyms
Glycogen; glycogen phosphorylase; glycogen storage disease type V; glycogen storage disease type V) ; McArdle syndrome; muscle; muscle (McArdle syndrome; myophosphorylase; phosphorylase
Gene Name
Phosphorylase, glycogen, muscle
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
Concentration
1 mg/ml
Dilution
WB 1:500~2000, IHC 1:2000
Form
PBS (PH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide.
Buffer
PBS (PH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide.
Function
Druggable Genome
Storage Conditions
Store 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
Gene ID URL
https://www.ncbi.nlm.nih.gov/gene/?term=5837
Uniprot URL
https://www.uniprot.org/uniprot/P11217
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