
LDHA Antibody
Defects in LDHA are the cause of glycogen storage disease type 11 (GSD11) [MIM:612933]. A metabolic disorder that results in exertional myoglobinuria, pain, cramps and easy fatigue.
Details
Recombinant Human L-lactate dehydrogenase A chain protein (5-323AA)
Product Name | LDHA Antibody |
---|---|
Supplier name | Cusabio |
Group (E.g. Primary) | Primary |
Concentration | 50ug |
Clonality | Polyclonal |
Colour | Clear solution |
Product Type | Antibodies |
Conjugate | Unconjugated |
Size | 100ug |
Species Reactivity | Human |
Host Species | Rabbit |
Applications | ELISA, IF, IHC, WB |
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 | L-lactate dehydrogenase A chain (LDH-A) (EC 1.1.1.27) (Cell proliferation-inducing gene 19 protein) (LDH muscle subunit) (LDH-M) (Renal carcinoma antigen NY-REN-59), LDHA |
Publications | Publication List |
Target/Antigen | LDHA |
Datasheet URL | View Datasheet |