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Key Documents

G8644

Sigma-Aldrich

D-(+)-Glucose solution

100 g/L in H2O, sterile-filtered, BioXtra, suitable for cell culture

Synonyme(s) :

D-Glucopyranose

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About This Item

Formule empirique (notation de Hill):
C6H12O6
Numéro CAS:
Poids moléculaire :
180.16
Numéro Beilstein :
1281608
Numéro MDL:
Code UNSPSC :
12352201
ID de substance PubChem :
Nomenclature NACRES :
NA.75

Stérilité

sterile-filtered

Niveau de qualité

Gamme de produits

BioXtra

Forme

solution

Concentration

100 g/L in H2O

Technique(s)

cell culture | mammalian: suitable

Impuretés

endotoxin, tested

Température de stockage

room temp

Chaîne SMILES 

OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@@H]1O

InChI

1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3-,4+,5-,6+/m1/s1

Clé InChI

WQZGKKKJIJFFOK-DVKNGEFBSA-N

Informations sur le gène

human ... PYGM(5837)

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Description générale

Glucose provides the primary energy source for cell metabolism. It is a main source of energy for living organisms. Glucose occurs naturally in the free state in fruits and other parts of plants. It is combined into glucosides, disaccharides, oligosaccharides, the polysaccharides (cellulose and starch), and glycogen.

Application

D-(+)-Glucose solution has been used:

  • to determine extracellular acidification rate (ECAR) or oxygen consumption rate (OCR) in human CB CD34+cells by Seahorse extracellular flux assay
  • as a negative control in human umbilical vein endothelial cell (HUVEC) culture
  • as a supplement for culturing colonic biopsies

Actions biochimiques/physiologiques

Glucose is an aldosic monosaccharide and acts as an important component of glycolysis and downstream pathways for aerobic and anaerobic respiration. It provides energy for growth and reproduction. Glucose is a byproduct of photosynthesis that is condensed to starch in plants and cyanobacteria.

Autres remarques

This product has been tested with cell lines to verify the product is not cytotoxic. The growth promoting capacity of this cell culture tested glucose solution was assessed at 45 mL/L in medium using appropriate cell lines.
This solution has been sterilized by filtration.

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Code de la classe de stockage

12 - Non Combustible Liquids

Classe de danger pour l'eau (WGK)

nwg

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable


Certificats d'analyse (COA)

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Consulter la Bibliothèque de documents

Shu J Lam et al.
ACS applied materials & interfaces, 8(49), 33446-33456 (2016-12-15)
'Structurally nanoengineered antimicrobial peptide polymers' (SNAPPs), in the form of star-shaped peptide polymer nanoparticles, have been recently demonstrated as a new class of antimicrobial agents with superior in vitro and in vivo efficacy against Gram-negative pathogens, including multidrug-resistant species. Herein
Brandon Mapes et al.
Physiological genomics, 46(8), 302-308 (2014-02-20)
1α,25-Dihydroxyvitamin D3 [1α,25(OH)2D3] is a steroid hormone derived from circulating 25(OH) vitamin D [25(OH)D] with chemopreventive effects in colorectal cancer. 1α,25(OH)2D3 acts through transcriptional mechanisms; however, our understanding of vitamin D transcriptional responses in the colon is derived from studies
Dieter Henrik Heiland et al.
Nature communications, 10(1), 2541-2541 (2019-06-13)
Reactive astrocytes evolve after brain injury, inflammatory and degenerative diseases, whereby they undergo transcriptomic re-programming. In malignant brain tumors, their function and crosstalk to other components of the environment is poorly understood. Here we report a distinct transcriptional phenotype of
Andreia V Pinho et al.
PloS one, 10(6), e0128012-e0128012 (2015-06-06)
Sirtuin 1 (Sirt1) has been reported to be a critical positive regulator of glucose-stimulated insulin secretion in pancreatic beta-cells. The effects on islet cells and blood glucose levels when Sirt1 is deleted specifically in the pancreas are still unclear. This
Rawand Masoud et al.
Cell reports. Medicine, 1(8), 100143-100143 (2020-12-10)
Mitochondrial respiration (oxidative phosphorylation, OXPHOS) is an emerging target in currently refractory cancers such as pancreatic ductal adenocarcinoma (PDAC). However, the variability of energetic metabolic adaptations between PDAC patients has not been assessed in functional investigations. In this work, we

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