ALDOA Polyclonal Antibody, Biotin Conjugated

Background
Plays a key role in glycolysis and gluconeogenesis. In addition, may also function as scaffolding protein . Defects in ALDOA are the cause of glycogen storage disease type 12 (GSD12) [MIM:611881]; also known as red cell aldolase deficiency. A metabolic disorder associated with increased hepatic glycogen and hemolytic anemia. It may lead to myopathy with exercise intolerance and rhabdomyolysis. Belongs to the class I fructose-bisphosphate aldolase family.

Description
ALDOA Polyclonal Antibody, Biotin Conjugated. Biotin. Raised in: Rabbit.

Formulation
Liquid. 0.03% Proclin 300. 50% Glycerol, 0.01M PBS, pH 7.4.

Specificity
Human

Isotype
IgG

Uniprot ID
P04075

Purification
Protein G purified

Immunogen
Recombinant Human Fructose-bisphosphate aldolase A protein (2-364AA)

Storage
Shipped at 4°C. Upon delivery aliquot and store at -20°C (short-term) or -80°C (long-term). Avoid repeated freeze.

Alternative Names
ALDOA, ALDA, Lung cancer antigen NY-LU-1, Muscle-type aldolase

Application
ELISA; Recommended dilution: ELISA 1:500-1:1000