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MAK223

Sigma-Aldrich

Aldolase Activity Colorimetric Assay Kit

Sufficient for 100 Colorimetric tests

Sinonimo/i:

Aldolase Colorimetric Assay Kit

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About This Item

Codice UNSPSC:
12161503
NACRES:
NA.84

Metodo di rivelazione

colorimetric

Malattie correlate

cancer; neurological disorders; hematological disorder

Temperatura di conservazione

−20°C

Informazioni sul gene

human ... ALDOA(226) , ALDOB(229) , ALDOC(230)
mouse ... ALDOA(11674) , ALDOB(230163) , ALDOC(11676)
rat ... ALDOA(24189) , ALDOB(24190) , ALDOC(24191)

Descrizione generale

Aldolase (fructose-bisphosphate aldolase; EC 4.1.2.13) catalyzes the reversible conversion of fructose-1,6-bisphosphate to glyceraldehyde 3-phosphate and dihydroxyacetone phosphate. Three isoforms of aldolase (A, B, and C) are differentially expressed during development. Aldolases have been recognized as positive regulators of the Wnt signaling pathway. Deficiency of aldolases is associated with myopathy and hemolytic anemia.

The Aldolase Activity Colorimetric Assay Kit is a simple and high throughput assay for measuring aldolase activity in serum, plasma, and a variety of tissues and cells. Aldolase activity is determined by measuring a colorimetric product with absorbance at 450 nm (A450) proportional to the enzymatic activity present. One unit of aldolase is the amount of enzyme that generates 1.0 μmole of NADH per minute at pH 7.2 at 37 °C.
Aldolase (fructose-bisphosphate aldolase; EC 4.1.2.13) catalyzes the reversible conversion of fructose-1,6-bisphosphate to glyceraldehyde 3-phosphate and dihydroxyacetone phosphate. Three isoforms of aldolase (A, B, and C) are differentially expressed during development. Aldolases have been recognized as positive regulators of the Wnt signaling pathway. Deficiency of aldolases is associated with myopathy and hemolytic anemia

Caratteristiche e vantaggi

Compatible with high-throughput handling systems.

Compatibilità

Suitable for the detection of Aldolase activity in biological samples such as tissue, cells, serum, and plasma.

Principio

The Aldolase Activity Colorimetric Assay Kit is a simple and high throughput assay for measuring aldolase activity in serum, plasma, and a variety of tissues and cells. Aldolase activity is determined by measuring a colorimetric product with absorbance at 450 nm (A450) proportional to the enzymatic activity present. One unit of aldolase is the amount of enzyme that generates 1.0 μmole of NADH per minute at pH 7.2 at 37 °C.

Solo come componenti del kit

N° Catalogo
Descrizione
  • Aldolase Assay Buffer
  • Aldolase Substrate
  • Aldolase Enzyme Mix
  • Aldolase Developer
  • NADH Standard
  • Aldolase Positive Control

Pittogrammi

Corrosion
GHS05

Avvertenze

Danger

Indicazioni di pericolo

H314,H412

Classi di pericolo

Aquatic Chronic 3 - Eye Dam. 1 - Skin Corr. 1B

Codice della classe di stoccaggio

8A - Combustible corrosive hazardous materials

Elenchi normativi

Forniamo informazioni su eventuali restrizioni prevalentemente per i prodotti chimici. Per altre tipologie di prodotto siamo in grado di fornire soltanto informazioni limitate. Nessuna segnalazione significa che nessuno dei componenti è citato in un elenco. È dovere dell’utilizzatore assicurarsi che il prodotto venga impiegato in maniera sicura e a norme di legge.

EU REACH Annex XIV (Authorisation List)

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Aldolase positively regulates of the canonical Wnt signaling pathway.
Caspi M, et al.
Molecular Cancer, 13(1), 164-164 (2014)
Human aldolase A natural mutants: relationship between flexibility of the C-terminal region and enzyme function.
Esposito G, et al.
The Biochemical Journal, 380(1), 51-56 (2004)
Unraveling the structural and functional features of an aldolase A mutant involved in the hemolytic anemia and severe rhabdomyolysis reported in a child.
Esposito G, et al.
Blood, 105(2), 905-906 (2005)
Zhenchang Guo et al.
Molecular & cellular proteomics : MCP, 20, 100053-100053 (2021-02-10)
Esophageal squamous cell carcinoma (ESCC) is an aggressive malignancy with poor therapeutic outcomes. However, the alterations in proteins and posttranslational modifications (PTMs) leading to the pathogenesis of ESCC remain unclear. Here, we provide the comprehensive characterization of the proteome, phosphorylome
Biochemical markers of muscular damage.
Brancaccio P, et al
Clinical Chemistry and Laboratory Medicine, 48(6), 757-767 (2010)
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