ALDOA Polyclonal Antibody (E-AB-10125)
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For research use only.
| Verified Samples |
Verified Samples in WB: A549, Hela Verified Samples in IHC: Human ovarian cancer, Human gastric cancer |
| Dilution | WB 1:500-1:2000, IHC 1:50-1:200 |
| Isotype | Rabbit IgG |
| Host | Rabbit |
| Reactivity | Human, Mouse, Rat |
| Applications | WB, IHC |
| Clonality | Polyclonal |
| Immunogen | Recombinant protein of human ALDOA |
| Abbre | ALDOA |
| Synonyms | 6-BISPHOSPHATE ALDOLASE A, ALDA, Aldo1, ALDOA, Aldolase, Aldolase 1, Aldolase A, Aldolase A fructose bisphosphatase, Aldolase A fructose bisphosphate, Epididymis secretory sperm binding protein Li 87p, FRUCTOALDOLASE A, Fructose 1 6 bisphosphate triosephosphate, Fructose 1 6 bisphosphate triosephosphate lyase, Fructose bisphosphate aldolase, Fructose bisphosphate aldolase A, FRUCTOSE-1, fructose-bisphosphate A, Fructose-bisphosphate aldolase A, Fructose-bisphosphate aldolase A Muscle-type, GSD12, HEL S 87p, Lung cancer antigen NY LU 1, Lung cancer antigen NY-LU-1, MGC10942, MGC17716, MGC17767, Muscle type aldolase, Muscle-type aldolase, RNALDOG5抗体 |
| Swissprot | |
| Calculated MW | 39 kDa |
| Cellular Localization | Cytoskeleton, actin cytoskeleton, Cytosol, Extracellular region or secreted, extracellular exosome, extracellular region, extracellular space, Nucleus, Other locations: ficolin-1-rich granule lumen, I band, M band, membrane, platelet alpha granule lumen, secretory granule lumen, sperm head, tertiary granule lumen. |
| Concentration | 0.3 mg/mL |
| Buffer | Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol. |
| Purification Method | Affinity purification |
| Research Areas | Cancer, Metabolism, Signal Transduction |
| Conjugation | Unconjugated |
| Storage | Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles. |
| Shipping | The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended. |
| background | The protein encoded by this gene, Aldolase A (fructose-bisphosphate aldolase), is a glycolytic enzyme that catalyzes the reversible conversion of fructose-1,6-bisphosphate to glyceraldehyde 3-phosphate and dihydroxyacetone phosphate. Three aldolase isozymes (A, B, and C), encoded by three different genes, are differentially expressed during development. Aldolase A is found in the developing embryo and is produced in even greater amounts in adult muscle. Aldolase A expression is repressed in adult liver, kidney and intestine and similar to aldolase C levels in brain and other nervous tissue. Aldolase A deficiency has been associated with myopathy and hemolytic anemia. Alternative splicing and alternative promoter usage results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 3 and 10. |
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