6-NBDG (6-(N-(7-Nitrobenz-2-oxa-1,3-diazol-4-yl)amino)-6-Deoxyglucose)
6-NBDG (6-(<i>N</i>-(7-Nitrobenz-2-oxa-1,3-diazol-4-yl)amino)-6-Deoxyglucose)
Invitrogen™

6-NBDG (6-(N-(7-Nitrobenz-2-oxa-1,3-diazol-4-yl)amino)-6-Deoxyglucose)

6-NBDG is a fluorescent nonhydrolyzable glucose analog that has been used to monitor glucose uptake and transport in live cells.Read more
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Catalog NumberQuantity
N231065 mg
Catalog number N23106
Price (USD)
516.00
Each
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Quantity:
5 mg
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Delivery information
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Price (USD)
516.00
Each
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6-NBDG is a fluorescent nonhydrolyzable glucose analog that has been used to monitor glucose uptake and transport in live cells. Although sensitive to its environment NBD fluorescence typically displays excitation/emission maxima of ∼465/540 nm and can be visualized using optical filters designed for fluorescein.
For Research Use Only. Not for use in diagnostic procedures.
Specifications
Description6-NBDG (6-(N-(7-Nitrobenz-2-oxa-1,3-diazol-4-yl)amino)-6-Deoxyglucose)
Detection MethodAbsorbance
FormSolid
Quantity5 mg
Shipping ConditionRoom Temperature
ColorOrange
Product LineLife Technologies
Unit SizeEach
Contents & Storage
Store in freezer at -5°C to -30°C and protect from light.
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Lot #Certificate TypeDateCatalog Number(s)
2930838Certificate of AnalysisMay 26, 2024N23106
2805751Certificate of AnalysisDec 27, 2023N23106
1846937Certificate of AnalysisJan 25, 2023N23106
2441494Certificate of AnalysisMay 24, 2022N23106
2300988Certificate of AnalysisJun 01, 2021N23106
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Safety Data Sheets

Frequently asked questions (FAQs)

Final concentrations of 2-NBDG can range from 10 µM to 600 µM; 100 µM to 600 µM have been used with bacteria and yeasts and, from 10 µM to 200 µM for primary and cultured mammalian cells.

Final concentrations of 6-NBDG may range from 30 µM up to 300 µM.

Cells should be incubated at the desired temperature and time to allow for sufficient detection of green-yellow fluorescence within cells. Uptake is temperature dependent. Incubation times may range from seconds up to 30 minutes or longer, dependent upon the final concentration of the reagent, cell type, culture conditions, and other factors.

Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

Compatible solvents (and approximate maximum solubility): DMSO ( ˜10 mg/mL), DMF (˜10 mg/mL), ethanol (˜20 mg/mL), methanol (˜20 mg/mL), H2O (˜10 mg/mL), PBS, pH 7.2 (˜10 mg/mL).

Stock solutions may be prepared using the recommended solvents in concentrations at or below their maximum solubility and then stored frozen, desiccated (for non-aqueous solvents), and protected from light. Aqueous solutions should not be stored longer than one day.

For long-term storage, these reagents should be stored as a solid at ≤–20°C. To make smaller aliquots, dissolve the reagent in ethanol, make smaller aliquots in separate vials and then evaporate the solvent using a vacuum pump. Do not use DMSO or DMF due to their low vapor pressure.

Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

Citations & References (23)

Citations & References
Abstract
Evaluation of glucose transport and its regulation by insulin in human monocytes using flow cytometry.
Authors:Dimitriadis G, Maratou E, Boutati E, Psarra K, Papasteriades C, Raptis SA
Journal:Cytometry A
PubMed ID:15688355
'BACKGROUND: We investigated the effects of insulin on glucose transport in human monocytes using flow cytometry, a method with several advantages over previously used techniques. We hypothesized that monocytes could be used as tools to study insulin action at the cellular level and facilitate the investigation of mechanisms that lead ... More
Glutamate triggers rapid glucose transport stimulation in astrocytes as evidenced by real-time confocal microscopy.
Authors:Loaiza A, Porras OH, Barros LF
Journal:J Neurosci
PubMed ID:12917367
'Glutamate stimulates glycolysis in astrocytes, a phenomenon that couples astrocytic metabolism with neuronal activity. However, it is not known whether glutamate also affects glucose transporter-1 (GLUT1), the transporter responsible for glucose entry into astrocytes. To address this question, two different real-time single-cell hexose uptake assays were applied to cultured hippocampal ... More
Net sugar transport is a multistep process. Evidence for cytosolic sugar binding sites in erythrocytes.
Authors:Cloherty EK, Sultzman LA, Zottola RJ, Carruthers A
Journal:Biochemistry
PubMed ID:7492539
'Human erythrocyte net sugar transport is hypothesized to be rate-limited by reduced cytosolic diffusion of sugars and/or by reversible sugar association with intracellular macromolecules [Naftalin, R.J., Smith, P.M., & Roselaar, S.E. (1985) Biochim. Biophys. Acta 820, 235-249]. The present study examines these hypotheses. Protein-mediated 3-O-methylglucose uptake at 4 degrees C ... More
Expression of GLUT-2 cDNA in human B lymphocytes: analysis of glucose transport using flow cytometry.
Authors:Rauchman MI, Wasserman JC, Cohen DM, Perkins DL, Hebert SC, Milford E, Gullans SR
Journal:Biochim Biophys Acta
PubMed ID:1420258
'The molecular characterization of transport proteins is often limited by transient functional expression or the need for a simple method to select functional cDNA clones. We used a mammalian expression system to obtain long-term expression of GLUT-2, an isoform of glucose permease. Rat GLUT-2 cDNA was ligated into an EBV ... More
Flow cytometric analysis of glucose transport by rat brain cells.
Authors:Aller CB, Ehmann S, Gilman-Sachs A, Snyder AK
Journal:Cytometry
PubMed ID:9041115
'The fluorescent, non-metabolizable glucose analog 6-[N-(7-nitrobenz-2-oxa-1,3-diazol-4-yl)amino]-6-deoxyglucose (NBDG) was used to measure rates of hexose transport by dissociated brain cells from developing and adult rats. Flow cytometric analysis of glucose uptake and expression of glucose transporters was performed by mapping on size by granularity, which discriminated between neurons and astrocytes in ... More
23 total citations

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