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For research use only.

Verified Samples Verified Samples in WB: Mouse liver
Verified Samples in IHC: Human cervical cancer, Human esophagus 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 Synthetic peptide of human ALDOB
Synonyms ALDB,  ALDO B,  ALDO2,  ALDOB,  Aldolase 2,  Aldolase B,  Aldolase B fructose bisphosphate,  Aldolase2,  AldolaseB,  EC 4.1.2.13,  Fructose bisphosphate aldolase B,  Fructose-bisphosphate aldolase B,  Liver type aldolase,  Liver-type aldolase,  MS1077
Swissprot
Calculated MW 39 kDa
Cellular Localization Cytoskeleton, centriolar satellite, microtubule organizing center, Cytosol, Extracellular region or secreted, extracellular exosome.
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 Fructose-1,6-bisphosphate aldolase (EC 4.1.2.13) is a tetrameric glycolytic enzyme that catalyzes the reversible conversion of fructose-1,6-bisphosphate to glyceraldehyde 3-phosphate and dihydroxyacetone phosphate. Vertebrates have 3 aldolase isozymes which are distinguished by their electrophoretic and catalytic properties. Differences indicate that aldolases A, B, and C are distinct proteins, the products of a family of related 'housekeeping' genes exhibiting developmentally regulated expression of the different isozymes. The developing embryo produces aldolase A, which is produced in even greater amounts in adult muscle where it can be as much as 5% of total cellular protein. In adult liver, kidney and intestine, aldolase A expression is repressed and aldolase B is produced. In brain and other nervous tissue, aldolase A and C are expressed about equally. There is a high degree of homology between aldolase A and C. Defects in ALDOB cause hereditary fructose intolerance.
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Unconjugated

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