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.