추천 제품
생물학적 소스
bacterial (Leuconostoc mesenteroides)
Quality Level
유형
Type XXIII
양식
ammonium sulfate suspension
특이 활성도
550-1,100 units/mg protein (biuret)
분자량
54 kDa
농도
≥2.0 mg/mL Biuret
외래 활성
6-Phosphogluconic dehydrogenase, hexokinase, NADH oxidase and NADPH oxidase ≤0.005%
PGI ≤0.01%
저장 온도
2-8°C
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관련 카테고리
일반 설명
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.
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.
애플리케이션
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.
생화학적/생리학적 작용
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.
단위 정의
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.
물리적 형태
Suspension in 2.7 M (NH4)2SO4 solution containing 42 mM Tris and 0.8 mM MgCl2
신호어
Danger
유해 및 위험 성명서
예방조치 성명서
Hazard Classifications
Resp. Sens. 1
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
Eyeshields, Gloves, type N95 (US)
가장 최신 버전 중 하나를 선택하세요:
시험 성적서(COA)
이미 열람한 고객
In vitro studies: inhibition of nevirapine metabolism by nortriptyline in hepatic microsomes
Bio-protocol, 5(19) (2014)
A novel type of chloroplast stromal hexokinase is the major glucose-phosphorylating enzyme in the moss Physcomitrella patens
The Journal of Biological Chemistry, 278(45), 44439-44447 (2003)
Lysine-21 of Leuconostoc mesenteroides glucose 6-phosphate dehydrogenase participates in substrate binding through charge-charge interaction
Protein Science, 1(3), 329-334 (1992)
Enzyme-stabilizing activity of seed trypsin inhibitors during desiccation
Plant Science, 142, 209-218 (1999)
Glucose-6-Phosphate Dehydrogenase Deficiency
StatPearls [Internet] (2022)
문서
Instructions for working with enzymes supplied as ammonium sulfate suspensions
프로토콜
To measure glucose-6-phosphate dehydrogenase activity, beta-nicotinamide adenine dinucleotide phosphate is used in a spectrophotometric rate determination assay at 340 nm.
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