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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 IgG
Host Rabbit
Reactivity Human,  Mouse,  Rat
Applications WB,  IHC
Clonality Polyclonal
Immunogen Recombinant protein of human ALDOA
Abbre ALDOA
Synonyms ALDA,  ALDOA,  Aldo1,  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-bisphosphate A
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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Unconjugated

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