PYGM 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.
NCBI Gene ID
5837
Swiss Prot
P11217
Host
Rabbit
Reactivity
Human, Mouse, Rat
Immunogen
A synthetic peptide corresponding to a sequence within amino acids 700 to the C-terminus of human PYGM (NP_005600.1) .
Clonality
Polyclonal
Conjugation
Unconjugated
Type
Primary Antibodies
Field of Research
Cancer, Signal Transduction
Purification
Affinity purification
Positive Control
Mouse skeletal muscle
Concentration
Batch dependent
Buffer
PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Modification
None
Shipping Conditions
Blue Ice
Storage Conditions
Store at -20˚ C. Avoid freeze / thaw cycles.
Calculated Molecular Weight
Observed: 100kDa
Fragment
IgG
Applications Notes
WB: 1:500 - 1:2000
Symbol
PYGM
Positive Control 2
Mouse brain
Positive Control 3
Mouse lung
Positive Control 4
Rat skeletal muscle
NCBI Official Name
Phosphorylase, glycogen, muscle
NCBI Organism
Homo sapiens
Other Product Names
PYGM, GPMM, Myophosphorylase, Phosphorylase, glycogen muscle
Tested Applications
WB
Physical Properties
Liquid
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