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Enhance your metabolic research with our Recombinant Human ALDOA protein, a crucial enzyme involved in glycolysis and gluconeogenesis. Fructose-bisphosphate aldolase A, encoded by the ALDOA gene, plays a vital role in energy production within cells by catalyzing the reversible cleavage of fructose-1,6-bisphosphate to dihydroxyacetone phosphate and glyceraldehyde-3-phosphate. This protein is also identified as a lung cancer antigen, NY-LU-1, making it relevant for cancer research. Our Recombinant Human ALDOA protein is expressed in an E.coli system and encompasses the full length of the mature protein, covering the 2-364aa region. The N-terminal GST-tag allows for effective protein purification, ensuring a high-quality product for your experiments. With a purity greater than 90% as confirmed by SDS-PAGE, this full-length ALDOA protein delivers the reliability you need. Select either liquid or lyophilized powder form to suit your specific laboratory requirements and propel your research forward.
Enhance your metabolic research with our Recombinant Human ALDOA protein, a crucial enzyme involved in glycolysis and gluconeogenesis. Fructose-bisphosphate aldolase A, encoded by the ALDOA gene, plays a vital role in energy production within cells by catalyzing the reversible cleavage of fructose-1,6-bisphosphate to dihydroxyacetone phosphate and glyceraldehyde-3-phosphate. This protein is also identified as a lung cancer antigen, NY-LU-1, making it relevant for cancer research.
Our Recombinant Human ALDOA protein is expressed in an E.coli system and encompasses the full length of the mature protein, covering the 2-364aa region. The N-terminal GST-tag allows for effective protein purification, ensuring a high-quality product for your experiments. With a purity greater than 90% as confirmed by SDS-PAGE, this full-length ALDOA protein delivers the reliability you need. Select either liquid or lyophilized powder form to suit your specific laboratory requirements and propel your research forward.
| Cat.No | ACP03088 | Target Name | ALDOA |
|---|---|---|---|
| Form | Liquid or Lyophilized powder | Expression System | E.coli |
| Expression Range | 2-364aa | Mol Weight | 66.3kDa |
| Protein Length | Full Length of Mature Protein | Purity | Greater than 90% as determined by SDS-PAGE. |
| Storage Buffer | 5%-50% glycerol. Lyophilized powder form: the buffer before lyophilization is Tris/PBS-based buffer, 6% Trehalose, Liquid form: default storage buffer is Tris/PBS-based buffer, pH 8.0. |
| Target Species | Human | Uniprot ID | P04075 |
|---|
Uniprot Id
P04075
Target Species
Human
Target Name
ALDOA
Target Full Name
Fructose-bisphosphate aldolase A
Target Function
Plays a key role in glycolysis and gluconeogenesis. In addition, may also function as scaffolding protein.
Target Involvement
Glycogen storage disease 12 (GSD12)
Target Subcellular Location
Cytoplasm, myofibril, sarcomere, I band. Cytoplasm, myofibril, sarcomere, M line.
Target Protein Families
Class I fructose-bisphosphate aldolase family
Target Research Area
Metabolism
Target Synonyms
ALDA; Aldo1; ALDOA; ALDOA_HUMAN; Aldolase 1; Aldolase A; Aldolase A fructose bisphosphatase; Aldolase A fructose bisphosphate; Aldolase; fructose-bisphosphate A; Epididymis secretory sperm binding protein Li 87p; FRUCTOALDOLASE A; Fructose 1 6 bisphosphate triosephosphate lyase; Fructose bisphosphate aldolase A; Fructose bisphosphate aldolase; FRUCTOSE-1,6-BISPHOSPHATE ALDOLASE 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
Target Background
This gene encodes a member of the class I fructose-bisphosphate aldolase protein family. The encoded protein 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. Mutations in this gene have been associated with Glycogen Storage Disease XII, an autosomal recessive disorder associated with hemolytic anemia. Disruption of this gene also plays a role in the progression of multiple types of cancers. Related pseudogenes have been identified on chromosomes 3 and 10.
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