PYGM (NM_001164716) Human Recombinant Protein
Selected Variant
PH33177M5
Size: 20 µg
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
Recombinant protein of human phosphorylase, glycogen, muscle (PYGM), transcript variant 2.
Synonyms
GSD5
Gene ID
5837
UniProt
P11217
Accession Number mRNA
NM_001164716
Chromosomal Location
11q13.1
Expression System
HEK293T
Tag
C-Myc/DDK
Related Pathways
Insulin signaling pathway, Starch and sucrose metabolism
Field of Research
Insulin signaling pathway, Starch and sucrose metabolism
Concentration
>50 ug/mL as determined by microplate BCA method
Purity
> 80% as determined by SDS-PAGE and Coomassie blue staining
Form
Liquid
Buffer
25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10% glycerol
Function
Druggable Genome
Molecular Weight
87.1 kDa
Storage Conditions
Stable for 1 year at -20°C or below from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. For long-term storage, aliquot and store at -20°C or below. Avoid repeated freeze-thaw cycles.
Symbol
PYGM
Species
Human
Protein ID
NP_001158188
Gene ID URL
https://www.ncbi.nlm.nih.gov/gene/5837
Uniprot URL
https://www.uniprot.org/uniprot/P11217
Accession Number mRNA URL
https://www.ncbi.nlm.nih.gov/nuccore/NM_001164716
Protein ID Link
https://www.ncbi.nlm.nih.gov/nuccore/NP_001158188
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