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Results for "

Aldolase 1

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    7
    TargetMol | Inhibitors_Agonists
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    1
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Aldolase A Protein, Mouse, Recombinant (His)
Muscle-type aldolase, Fructose-bisphosphate aldolase A, Aldolase 1, Aldoa, Aldo1
TMPH-02662
Plays a key role in glycolysis and gluconeogenesis. In addition, may also function as scaffolding protein. Aldolase A Protein, Mouse, Recombinant (His) is expressed in Baculovirus insect cells with C-6xHis tag. The predicted molecular weight is 40.3 kDa and the accession number is P05064.
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20 days
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Aldolase A Protein, Mouse, Recombinant (His & Myc)
Muscle-type aldolase, Fructose-bisphosphate aldolase A, Aldolase 1, Aldoa, Aldo1
TMPH-02663
Plays a key role in glycolysis and gluconeogenesis. In addition, may also function as scaffolding protein. Aldolase A Protein, Mouse, Recombinant (His & Myc) is expressed in E. coli expression system with N-10xHis and C-Myc tag. The predicted molecular weight is 46.7 kDa and the accession number is P05064.
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20 days
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CYP17A1 Protein, Human, Recombinant (GST)
Steroid 17-alpha-monooxygenase, Steroid 17-alpha-hydroxylase 17,20 lyase, S17AH, Cytochrome P450-C17 (Cytochrome P450c17), Cytochrome P450 17A1, CYPXVII, CYP17A1, CYP17, 20 lyase, 17-alpha-hydroxyprogesterone aldolase
TMPH-02139
A cytochrome P450 monooxygenase involved in corticoid and androgen biosynthesis. Catalyzes 17-alpha hydroxylation of C21 steroids, which is common for both pathways. A second oxidative step, required only for androgen synthesis, involves an acyl-carbon cleavage. The 17-alpha hydroxy intermediates, as part of adrenal glucocorticoids biosynthesis pathway, are precursors of cortisol (Probable). Hydroxylates steroid hormones, pregnenolone and progesterone to form 17-alpha hydroxy metabolites, followed by the cleavage of the C17-C20 bond to form C19 steroids, dehydroepiandrosterone (DHEA) and androstenedione. Has 16-alpha hydroxylase activity. Catalyzes 16-alpha hydroxylation of 17-alpha hydroxy pregnenolone, followed by the cleavage of the C17-C20 bond to form 16-alpha-hydroxy DHEA. Also 16-alpha hydroxylates androgens, relevant for estriol synthesis. Mechanistically, uses molecular oxygen inserting one oxygen atom into a substrate, and reducing the second into a water molecule, with two electrons provided by NADPH via cytochrome P450 reductase (CPR; NADPH-ferrihemoprotein reductase).
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20 days
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ALDOA Protein, Human, Recombinant (His)
Muscle-type aldolase, Lung cancer antigen NY-LU-1, Fructose-bisphosphate aldolase A, ALDOA, ALDA
TMPH-01357
Plays a key role in glycolysis and gluconeogenesis. In addition, may also function as scaffolding protein. ALDOA Protein, Human, Recombinant (His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 45.3 kDa and the accession number is P04075.
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20 days
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ALDOC Protein, Human, Recombinant (His)
zebrin II, Scrg2, Fructose-bisphosphate aldolase C, Brain-type aldolase, Aldolase C, Aldo3, ALDC
TMPJ-00818
Fructose-bisphosphate aldolase C (ALDOC) belongs to the class I fructose-bisphosphate aldolase family. It is an enzyme that, in humans, is encoded by the ALDOC gene. ALDOC is expressed exclusively in the hippocampus and Purkinje cells of the brain. ALDOC is a glycolytic enzyme which catalyzes the reversible aldol cleavage of fructose-1,6-biphosphate and fructose 1-phosphate to dihydroxyacetone phosphate and either glyceraldehyde-3-phosphate or glyceraldehydes respectively
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7-10 days
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Aldolase B Protein, Human, Recombinant (GST)
aldolase B, fructose-bisphosphate, ALDO2, ALDB
TMPY-02622
The aldolase family members involved in metabolism and glycolysis are present in three isoforms: ALDOA, ALDOB, and ALDOC. Aldolases are differentially expressed in human tissues, and aberrant expression has been observed in several human diseases and cancer types. Via GATA6, metastatic cells in the liver upregulate the enzyme aldolase B (ALDOB), which enhances fructose metabolism and provides fuel for major pathways of central carbon metabolism during tumor cell proliferation. Targeting ALDOB or reducing dietary fructose significantly reduces liver metastatic growth but has little effect on the primary tumor. Hereditary fructose intolerance (HFI) is an autosomal recessive disorder caused by aldolase B (ALDOB) deficiency resulting in an inability to metabolize fructose. The toxic accumulation of intermediate fructose-1-phosphate causes multiple metabolic disturbances, including postprandial hypoglycemia, lactic acidosis, electrolyte disturbance, and liver kidney dysfunction.
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7-10 days
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SPR-compatible buffer
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FBA1 Protein, Candida albicans, Recombinant (His & Myc)
IgE-binding allergen, Fructose-bisphosphate aldolase, Fructose-1,6-bisphosphate aldolase, FBPA, FBP aldolase, FBA1, 37 kDa major allergen
TMPH-00335
Catalyzes the aldol condensation of dihydroxyacetone phosphate (DHAP or glycerone-phosphate) with glyceraldehyde 3-phosphate (G3P) to form fructose 1,6-bisphosphate (FBP) in gluconeogenesis and the reverse reaction in glycolysis. FBA1 Protein, Candida albicans, Recombinant (His & Myc) is expressed in E. coli expression system with N-10xHis and C-Myc tag. The predicted molecular weight is 46.5 kDa and the accession number is Q9URB4.
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20 days
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