PYGM Polyclonal Antibody
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.
Abbreviation
PYGM
UniProt
P11217
Host
Rabbit
Reactivity
Human; Mouse; Rat
Immunogen
Recombinant protein of human PYGM
Target
Glycogen phosphorylase; Glycogen phosphorylase muscle form; muscle form; Muscpho; Myophosphorylase; Phosphorylase glycogen muscle (McArdle syndrome glycogen storage disease type V) ; Pygm; PYGM
Clonality
Polyclonal
Conjugation
Unconjugated
Applications
WB; IHC
Field of Research
Cancer; Metabolism; Signal Transduction
Purification
Affinity purification
Concentration
0.4 mg/mL
Dilution
WB 1:500-1:2000; IHC 1:30-1:150
Buffer
PBS with 0.05% sodium azide and 50% glycerol, PH7.4
Shipping Conditions
The product is shipped with ice pack, upon receipt, store it immediately at the temperature recommended.
Storage Conditions
Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.
Calculated Molecular Weight
97kDa
Isotype
IgG
Available Sizes
Frequently Asked Questions
More Discoveries
Explore Other Products
Browse additional items from our catalog
K1668902 1.0 µg DNA
PLGLB2 sgRNA CRISPR Lentivector (Human) (Target 1)
Sign In for Pricing
View Details 
MBS2165582-01 0.1 mL
APC-Linked Polyclonal Antibody to Microfibrillar Associated Protein 3 (MFAP3)
Sign In for Pricing
View Details MBS2165582-02 0.2 mL
APC-Linked Polyclonal Antibody to Microfibrillar Associated Protein 3 (MFAP3)
Sign In for Pricing
View Details MBS2165582-03 0.5 mL
APC-Linked Polyclonal Antibody to Microfibrillar Associated Protein 3 (MFAP3)
Sign In for Pricing
View Details