
ALDOA Antibody, FITC conjugated
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.
Details
Recombinant Human Fructose-bisphosphate aldolase A protein (2-364AA)
Product Name | ALDOA Antibody, FITC conjugated |
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Supplier name | Cusabio |
Group (E.g. Primary) | Primary |
Concentration | 50ug |
Clonality | Polyclonal |
Colour | Clear solution |
Product Type | Antibodies |
Conjugate | FITC |
Size | 100ug |
Species Reactivity | Human |
Host Species | Rabbit |
Applications | ELISA |
Storage/Storage buffer | Preservative: 0.03% Proclin 300<br />Constituents: 50% Glycerol, 0.01M PBS, PH 7.4 |
Form | Liquid |
Purification | >95%, Protein G purified |
Isotype | IgG |
Aliases | Fructose-bisphosphate aldolase A (EC 4.1.2.13) (Lung cancer antigen NY-LU-1) (Muscle-type aldolase), ALDOA, ALDA |
Publications | Publication List |
Target/Antigen | ALDOA |
Datasheet URL | View Datasheet |