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G7134

Sigma-Aldrich

L-(−)-Galactose

≥99% (HPLC)

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About This Item

Empirische Formel (Hill-System):
C6H12O6
CAS-Nummer:
15572-79-9
Molekulargewicht:
180.16
Beilstein:
1724622
EG-Nummer:
239-630-8
MDL-Nummer:
MFCD00063833
UNSPSC-Code:
12352201
PubChem Substanz-ID:
24895293
NACRES:
NA.25

Assay

≥99% (HPLC)

Form

powder

Methode(n)

HPLC: suitable

Farbe

white

Löslichkeit

water: 50 mg/mL, clear, colorless

SMILES String

OC[C@@H]1OC(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?/m0/s1

InChIKey

WQZGKKKJIJFFOK-DHVFOXMCSA-N

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Biochem./physiol. Wirkung

L-Galactose was shown to be a key intermediate in the molecular pathway of converting D-glucose to oxalic acid in Pistia stratiotes.

Sonstige Hinweise

To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)

Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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

Millipore

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USP

USP

1287700

Galactose

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Sigma-Aldrich

220477

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D-(+)-Galactose ≥99% (HPLC), BioReagent, suitable for cell culture, suitable for insect cell culture

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Supelco

93183

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D-(+)-Fucose ≥97% (GC)

Sigma-Aldrich

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D-(+)-Fucose

Minoru Tomizawa et al.
Oncology letters, 14(1), 899-902 (2017-07-12)
Tissues surrounding hepatocellular carcinomas (HCCs) lack glucose. Hepatocyte selection medium (HSM) is deficient in glucose and is supplemented with galactose. HCC cells were cultured in HSM to investigate the stem cell markers α-fetoprotein (AFP) and cluster of differentiation 44 (CD44).
Patrick Hossler et al.
mAbs, 9(4), 715-734 (2017-04-05)
Protein glycosylation is arguably the paramount post-translational modification on recombinant glycoproteins, and highly cited in the literature for affecting the physiochemical properties and the efficacy of recombinant glycoprotein therapeutics. Glycosylation of human immunoglobulins follows a reasonably well-understood metabolic pathway, which
S E Keates et al.
Phytochemistry, 53(4), 433-440 (2000-03-24)
Axenic Pistia stratiotes L. plants were pulse-chase labeled with [14C]oxalic acid, L[1-14C]ascorbic acid, L-6-14C]ascorbic acid, D-[1-14C]erythorbic acid, L-[1-14C]galactose, or [1-14C]glycolate. Specific radioactivities of L-ascorbic acid (AsA), free oxalic acid (OxA) and calcium oxalate (CaOx) in labeled plants were compared. Samples
Mili Thakur et al.
Scientific reports, 7(1), 231-231 (2017-03-24)
Premature ovarian insufficiency (POI) is a frequent long-term complication of classic galactosemia. The majority of women with this disorder develop POI, however rare spontaneous pregnancies have been reported. Here, we evaluate the effect of D-galactose and its metabolites, galactitol and
Dimitri Daudu et al.
Frontiers in plant science, 8, 1614-1614 (2017-10-06)
Cytokinin signaling is a key regulatory pathway of many aspects in plant development and environmental stresses. Herein, we initiated the identification and functional characterization of the five CHASE-containing histidine kinases (CHK) in the economically important
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