PYGM Mouse Monoclonal Antibody [Clone ID: LBI3F9]

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

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

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 1:2000, 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.