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PYGM Rabbit anti-Human, Polyclonal, Invitrogen™

Rabbit Polyclonal Antibody

Supplier:  Thermo Scientific PA511511

Catalog No. PIPA511511


Description

Description

This antibody is predicted to react with non-human primate based on sequence homology.

PYGM catalyzes and regulates the breakdown of glycogen to glucose-1-phosphate. Defects in PYGM are the cause of glycogen storage disease type 5 (GSD5), also known as McArdle disease. GSD5 is a metabolic disorder resulting in myopathy characterized by exercise intolerance, cramps, muscle weakness and recurrent myoglobinuria.
TRUSTED_SUSTAINABILITY
Specifications

Specifications

PYGM
Polyclonal
PYGM
Glycogen phosphorylase; muscle form; Myophosphorylase; PYGM;
Rabbit
Ammonium sulfate precipitation, Size-exclusion - Dialysis
RUO
5837
-20° C, Avoid Freeze/Thaw Cycles
Liquid
Immunohistochemistry (Paraffin), Western Blot
Unconjugated
P11217
PYGM
KLH conjugated synthetic peptide between 698-727 amino acids from the C-terminal region of human PYGM
400 μL
Primary
Human
Antibody
IgG
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