Merck
Todas as fotos(4)

G0625

Sigma-Aldrich

D-(+)-Galactose

≥98%

Sinônimo(s):
Galactose
Empirical Formula (Hill Notation):
C6H12O6
Número CAS:
Peso molecular:
180.16
Beilstein:
1724619
Número EC:
Número MDL:
ID de substância PubChem:
NACRES:
NA.21

fonte biológica

bovine (Ruminant- Cow, Ox, Buffalo)

Nível de qualidade

Ensaio

≥98%

forma

powder

technique(s)

HPLC: suitable

cor

white to off-white

useful pH range

5.0-7 (25 °C, 180 g/L)

pf

168-170 °C (lit.)

solubilidade

water: 180 g/L at 20 °C (68 °F )

SMILES string

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

InChI

1S/C6H12O6/c7-1-3(9)5(11)6(12)4(10)2-8/h1,3-6,8-12H,2H2/t3-,4+,5+,6-/m0/s1

InChI key

GZCGUPFRVQAUEE-KCDKBNATSA-N

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Este Item
G075048260G5388
D-(+)-Galactose ≥98%

Sigma-Aldrich

G0625

D-(+)-Galactose

D-(+)-Galactose ≥99%

Sigma-Aldrich

G0750

D-(+)-Galactose

D-(+)-Galactose suitable for microbiology, ≥99.0%

Millipore

48260

D-(+)-Galactose

D-(+)-Galactose powder, anhydrous, BioReagent, suitable for cell culture, suitable for insect cell culture

Sigma-Aldrich

G5388

D-(+)-Galactose

assay

≥98%

assay

≥99%

assay

≥99.0% (sum of enantiomers, HPLC)

assay

≥99%

form

powder

form

powder

form

powder

form

powder

technique(s)

HPLC: suitable

technique(s)

HPLC: suitable

technique(s)

-

technique(s)

cell culture | insect: suitable, cell culture | mammalian: suitable

mp

168-170 °C (lit.)

mp

168-170 °C (lit.)

mp

167-170 °C (dec.), 168-170 °C (lit.)

mp

168-170 °C (lit.)

Quality Level

300

Quality Level

300

Quality Level

200

Quality Level

200

Descrição geral

D-Galactose, the C-4 epimer of glucose and a pivotal mammalian monosaccharide, is widely present in blood, milk, gangliosides, and N- and O-linked glycans. It is ubiquitous in both plants and animals and acts as a constituent in diverse polysaccharides, including galactomannans, carrageenans, Agar (L-Galactose), Hemicellulose, and galactans. As an aldohexose, it serves as an energy source and a crucial element in glycolipids and glycoproteins. D-galactose undergoes enzymatic conversion into D-glucose for metabolism or polysaccharide storage, representing a C-4 epimer of glucose.

Furthermore, galactose is a fundamental component of the disaccharide lactose and is released through hydrolysis by β-galactosidase enzymes, playing a vital role in the survival and virulence of bacteria. In Escherichia coli, galactose is utilized through the Leloir pathway, with β-d-galactose serving as a carbon source and β-d-galactose inducing UDP-galactose synthesis for biosynthetic glycosylation. Galactose finds applications in researching metabolic disorders like galactosemia and serves as a substrate for enzymes involved in galactose catabolism, making it a valuable component in galactosyltransferase labeling buffer and a supplement in MRS broth for the growth of thermophilic lactobacilli.
D-galactose, an aldohexose, is a reducing sugar found naturally in the body. It is present in dairy products and the pectin of some fruits like plums, cherries, and kiwi. D-galactose is also found in certain vegetables, chestnuts, and some herbs.

Aplicação

D-(+)-Galactose has been used:
  • as a supplement in SGal media to grow yeast strains to examine the role of different Ssa heat-shock proteins (Hsp70) isoforms in Hsp90 chaperoning functions
  • as a carbon source in Biolog (MT2) microplate assay to test the ability of isolates to utilize carbon substrates
  • to induce expression of membrane protein-green fluorescent protein (GFP) fusion in yeast

D-Galactose is an energy source and a metabolite that finds application in cell biology, metabolomics and biochemical research.

Ações bioquímicas/fisiológicas

Galactose is a simple monosaccharide that serves as an energy source and as an essential component of glycolipids and glycoproteins. Galactose contributes to energy metabolism via its conversion to glucose by the enzymes that constitute the Leloir pathway. Defects in the genes encoding these proteins lead to the metabolic disorder galactosemia.
Metabolism of D-galactose leads to the formation of reactive oxygen species (ROS) and results in oxidative stress and hepatocyte damage.

Características e benefícios

  • Ideal for Metabolomics, Biochemical and Cell Biology research
  • Versatile and adaptable for wide variety of laboratory and research applications

Código de classe de armazenamento

11 - Combustible Solids

WGK

WGK 3

Ponto de fulgor (ºF)

Not applicable

Ponto de fulgor (ºC)

Not applicable

Equipamento de proteção individual

Eyeshields, Gloves, type N95 (US)


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Microbial cell factories, 10, 4-4 (2011-02-01)
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It has been previously shown that the long-term inhibition of milking-induced prolactin (PRL) release by quinagolide (QN), a dopamine agonist, reduces milk yield in dairy cows. To further demonstrate that PRL is galactopoietic in cows, we performed a short-term experiment

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