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About This Item
Empirical Formula (Hill Notation):
C6H12O6
CAS Number:
Molecular Weight:
180.16
UNSPSC Code:
12352201
NACRES:
NA.21
PubChem Substance ID:
EC Number:
200-416-4
Beilstein/REAXYS Number:
1724619
MDL number:
biological source
bovine (Ruminant- Cow, Ox, Buffalo)
assay
≥98% (HPLC)
form
powder
Quality Level
technique(s)
cell based assay: suitable
color
white to off-white
useful pH range
5.0-7 (25 °C, 180 g/L)
solubility
water: 180 g/L at 20 °C (68 °F )
application(s)
cell analysis
genomic analysis
life science and biopharma
storage temp.
room temp
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General description
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.
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.
Application
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.
Biochem/physiol Actions
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.
Features and Benefits
- Ideal for Metabolomics, Biochemical and Cell Biology research
- Versatile and adaptable for wide variety of laboratory and research applications
Other Notes
For additional information on our range of Biochemicals, please complete this form.
To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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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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