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DT Diaphorase (NQO1) human

SIGMA/D1315 - lyophilized powder, recombinant, expressed in E. coli, ≥90% (SDS-PAGE)

Synonym: DTD; NQO1; Quinone reductase

MDL Number: MFCD00130947
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-D1315-1MG 1 mg
$358.00
1/EA
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DT diaphorase (NQO1) is a homodimeric flavoprotein that catalyzes the direct two-electron reduction of quinones such as menadione.
SDS-PAGE DT Diaphorase (NQO1) Human (Cat. No. D1315) was assessed on SDS-PAGE.

 

assay ≥90% (SDS-PAGE)
form lyophilized powder
mol wt monomer 31000
Quality Level 200 
recombinant expressed in E. coli
specific activity ≥100 units/mg protein
storage temp. 2-8°C
UniProt accession no. P15559 
Application: Human DT diaphorase has been used in a study to assess the development of novel quinone phosphorodiamidate prodrugs. Human DT diaphorase has also been used to investigate its crystal structure for the development of a model for its interaction with the cytotoxic prodrug 5-(aziridin-1-yl)-2,4-dinitrobenzamide (CB1954).
Biochem/physiol Actions: DT-diaphorase, also referred to as NAD(P)H:(quinone-acceptor) oxidoreductase, is involved in the reductive activation process of several cytotoxic antitumor quinones and nitrobenzenes. It catalyzes the two-electron reduction of quinones and quinonoid compounds to hydroquinones, using either NADH or NADPH as the electron donor. The flavoenzyme contains one mole of FAD per mole of enzyme.
Biochem/physiol Actions: NQO1 is a cytosolic homodimeric FAD-dependent enzyme that catalyses the reduction of a broad range of cytotoxic quinones resulting in protection from cellular oxidative stress. Oxidative stress may also enhance NQO1-mediated protection of p53 and p73 against proteasomal degredation. The highly Inducible expression of NQO1 is controlled by the Nrf2-Keap1/ARE pathway and appears to be affected by changes in susceptibility to oxidative stress. During Oxygen/glucose deprivation, NQO1 appears to be involved in AMPK-induced cancer cell death. NQO1 has been observed to be overexpressed in several types of solid tumors, including breast, pancreas, lung and colon cancer.
Biochem/physiol Actions: Shown to activate quinone based anti-tumor agents in vivo. Suitable for conjugation to carrier molecules.
Other Notes: One unit will reduce 1.0 μmole cytochrome C per min/mg in the presence of menadione substrate at 37 °C.
RIDADR NONH for all modes of transport
WGK Germany WGK 3
Flash Point(F) Not applicable
Flash Point(C) Not applicable
Purity ≥90% (SDS-PAGE)
activity specific activity: ≥100 units/mg protein
Storage Temp. 2-8°C
Enzyme Commission (EC) Number 1.6.5.2   ( BRENDA  | IUBMB  )
UNSPSC 12352204

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