ALDOB Polyclonal Antibody
€0.00
In stock
SKU
E-AB-63750
Catalog Number: E-AB-63750
Isotype: Rabbit IgG
Reactivity: human, mouse, rat
Applications: WB
Datasheet, Questions? Contact us!
Isotype: Rabbit IgG
Reactivity: human, mouse, rat
Applications: WB
Datasheet, Questions? Contact us!
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.
Research Area: Cancer, Metabolism, Signal Transduction
Synonyms:
ALDOB, ALDB, ALDO2
Immunogen: Recombinant fusion protein of human ALDOB (NP_000026.2).
Swissprot: P05062
Gene ID: 229
Calculated MW: 39 kDa
Observed MW: 39 kDa
Purification Method: Affinity purification
Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3
Concentration: 1 mg/mL
Dilution: "WB 1:1000-1:2000"
Storage:
Store at -20°C. Avoid freeze / thaw cycles.
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.
Research Area: Cancer, Metabolism, Signal Transduction
Synonyms:
ALDOB, ALDB, ALDO2
Immunogen: Recombinant fusion protein of human ALDOB (NP_000026.2).
Swissprot: P05062
Gene ID: 229
Calculated MW: 39 kDa
Observed MW: 39 kDa
Purification Method: Affinity purification
Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3
Concentration: 1 mg/mL
Dilution: "WB 1:1000-1:2000"
Storage:
Store at -20°C. Avoid freeze / thaw cycles.
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