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Merck

G5760

Sigma-Aldrich

Glucose-6-phosphate Dehydrogenase from Leuconostoc mesenteroides

Type XXIII, ammonium sulfate suspension, 550-1,100 units/mg protein (biuret), ≥2.0 mg/mL Biuret

Synonim(y):

G-6-P-DH

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About This Item

Numer CAS:
Numer EC enzymu:
Numer WE:
Numer MDL:
Kod UNSPSC:
12352204
NACRES:
NA.54

pochodzenie biologiczne

bacterial (Leuconostoc mesenteroides)

Poziom jakości

typ

Type XXIII

Postać

ammonium sulfate suspension

aktywność właściwa

550-1,100 units/mg protein (biuret)

masa cząsteczkowa

54 kDa

stężenie

≥2.0 mg/mL Biuret

obecność zanieczyszczeń

6-Phosphogluconic dehydrogenase, hexokinase, NADH oxidase and NADPH oxidase ≤0.005%
PGI ≤0.01%

temp. przechowywania

2-8°C

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Opis ogólny

Research area: Cell Signaling

Glucose-6-phosphate dehydrogenase (G6PD) is found in the cytoplasm of all cells. The G6PD enzyme is encoded by the Gd gene, located on the long arm of the X chromosome.Glucose-6-phosphate Dehydrogenase (G6PD) from Leuconostoc mesenteroides catalyzes the oxidation of glucose 6-phosphate in the presence of nicotinamide adenine dinucleotide (NAD+) or nicotinamide adenine dinucleotide phosphate (NADP+). It corresponds to a molecular weight of 54 kDa and exists as a homodimer.

Zastosowanie

Glucose-6-phosphate Dehydrogenase from Leuconostoc mesenteroides has been used:

  • as a component of reaction mixture for assaying mannose- and glucose-6-phosphate activity
  • as a component of reaction mixture in the nevirapine inhibition studies in human hepatic microsomes
  • in the glucose-phosphorylating activity of chloroplast extracts
  • as a model to test the effect of seed protein fractions on enzyme protection during dehydration.
  • in assays for nicotinamide adenine dinucleotide and tissue pyridine nucleotides.

Działania biochem./fizjol.

Glucose-6-phosphate dehydrogenase (G6PD) catalyzes the conversion of glucose-6-phosphate to 6-phosphogluconolacetone as the first step in the pentose phosphate pathway.
Glucose-6-phosphate dehydrogenase (G6PD) is a housekeeping enzyme that protects cells from damage caused by reactive oxygen species by supplying substrates that help prevent oxidative harm. G6PD from Leuconostoc mesenteroides catalyzes the oxidation of glucose 6-phosphate in the presence of nicotinamide adenine dinucleotide (NAD+) or nicotinamide adenine dinucleotide phosphate (NADP+) as the first step in the pentose phosphate pathway. Lysine 21 in the Glucose-6-phosphate Dehydrogenase (G6PD) is crucial for binding NAD+. G6PD uses NAD+ or NADP+ based on the catabolic or anabolic metabolic pathway.G6PD deficiency can lead to acute hemolysis, neonatal jaundice, or severe chronic non-spherocytic hemolytic anemia.

Definicja jednostki

One unit will oxidize 1.0 μmole of D-glucose 6-phosphate to 6-phospho-D-gluconate per min in the presence of NAD at pH 7.8 at 30 °C.

Postać fizyczna

Suspension in 2.7 M (NH4)2SO4 solution containing 42 mM Tris and 0.8 mM MgCl2
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Piktogramy

Health hazard

Hasło ostrzegawcze

Danger

Zwroty wskazujące rodzaj zagrożenia

Zwroty wskazujące środki ostrożności

Klasyfikacja zagrożeń

Resp. Sens. 1

Kod klasy składowania

11 - Combustible Solids

Klasa zagrożenia wodnego (WGK)

WGK 3

Temperatura zapłonu (°F)

Not applicable

Temperatura zapłonu (°C)

Not applicable

Środki ochrony indywidualnej

Eyeshields, Gloves, type N95 (US)


Certyfikaty analizy (CoA)

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Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.

Odwiedź Bibliotekę dokumentów

A novel type of chloroplast stromal hexokinase is the major glucose-phosphorylating enzyme in the moss Physcomitrella patens
Olsson T, et al.
The Journal of Biological Chemistry, 278(45), 44439-44447 (2003)
In vitro studies: inhibition of nevirapine metabolism by nortriptyline in hepatic microsomes
Usach I and Peris JE
Bio-protocol, 5(19) (2014)
Oligomerization studies of Leuconostoc mesenteroides G6PD activity after SDS-PAGE and blotting
Ravera S, et al.
Molecular Biology, 44(3), 415-419 (2010)
Lysine-21 of Leuconostoc mesenteroides glucose 6-phosphate dehydrogenase participates in substrate binding through charge-charge interaction
Lee WT and Levy HR
Protein Science, 1(3), 329-334 (1992)
A Modified Method for Detection of Post-Phoretic Activities in Mannose-(Mpi, EC 5.3. 1.8) and Glucose-(Gpi, EC 5.3. 1.9) 6-Phosphate Isomerases
Zasypkin MY, et al.
Russian Journal of Genetics, 37(5), 581-583 (2001)

Produkty

Instructions for working with enzymes supplied as ammonium sulfate suspensions

Protokoły

Enzymatic Assay of Glucose-6-Phosphate Dehydrogenase (EC 1.1.1.49)

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