Glucose Uptake Assay Kit (Cell-based) (ab204702)
Key features and details
- Assay type: Cell-based
- Detection method: Fluorescent
- Platform: Microplate reader, Fluor. microscope, Flow cyt.
- Assay time: 40 min
- Sample type: Adherent cells, Suspension cells
Overview
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Product name
Glucose Uptake Assay Kit (Cell-based)
See all Glucose kits -
Detection method
Fluorescent -
Sample type
Adherent cells, Suspension cells -
Assay type
Cell-based -
Assay time
0h 40m -
Species reactivity
Reacts with: Mammals, Other species -
Product overview
Glucose Uptake Assay Kit (Cell-based) (ab204702) is an easy-to-use, non-radioactive kit that allows imaging and accurate measurement of glucose uptake in cultured cells in response to insulin and growth factors.
The glucose uptake assay protocol is based on a fluorescent glucose analog, which just like glucose can be taken up by cells through glucose transporters. However, this glucose analog cannot be fully utilized in glycolysis because of its modification and thus accumulates inside the cells. Fluorescence generated by the fluorescent glucose analog is proportional to the glucose uptake by the cells and can be used to measure glucose uptake using fluorescent microscopy and flow cytometry.
The kit includes phloretin, a natural phenol that inhibits glucose uptake, to use with control samples.
Glucose uptake assay protocol summary:
- remove cell culture media, and add glucose uptake mix to cells
- incubate for 30 min at 37ºC
- collect cells and keep on ice
- wash with analysis buffer
- analyze with flow cytometer or fluorescent microscope -
Notes
This product is manufactured by BioVision, an Abcam company and was previously called K681 GluTracker™ Glucose Uptake Assay Kit (Cell-Based). K681-50 is the same size as the 50 test size of ab204702.
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Platform
Microplate reader, Fluor. microscope, Flow cyt.
Properties
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Storage instructions
Store at -20°C. Please refer to protocols. -
Components 50 tests 100X GluTracker Reagent 1 x 200µl 100X Phloretin 1 x 75µl Buffer I 1 x 1.8ml Glucose Uptake Enhancer 1 x 1ml -
Research areas
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Relevance
Glucose (C6H12O6; FW: 180.16) is a ubiquitous energy source in most organisms, from bacteria to humans. The breakdown of carbohydrates produces mono- and disaccharides, most of which is glucose. Through glycolysis and TCA (citric acid cycle), glucose is oxidized to eventually form CO2 and water, generating the universal energy molecule ATP. Glucose is a primary source of energy for the brain and a critical component in the production of proteins and in lipid metabolism and therefore measurement of glucose level is a key diagnostic parameter for many metabolic disorders.
Images
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Comparison of histogram from flow analysis showing the inhibition of glucose uptake by phloretin in Jurkat cells (Black: negative control cells; orange: in the presence of phloretin; blue: without phloretin).
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Images of Jurkat cells obtained using fluorescent microscope (Top: treated with phloretin; Bottom: without phloretin treatment).
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Glucose Uptake in HeLa cells: HeLa cells showing the uptake of GluTracker Reagent in the cytoplasm. Cells were stained with GluTracker Reagent for 30 minutes and fixed. Image was taken using a fluorescent microscope with a 60X objective lens.
Datasheets and documents
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SDS download
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Datasheet download
References (4)
ab204702 has been referenced in 4 publications.
- Deng C et al. Bioceramic Scaffolds with Antioxidative Functions for ROS Scavenging and Osteochondral Regeneration. Adv Sci (Weinh) 9:e2105727 (2022). PubMed: 35182053
- Sposato V et al. The Medial Septum Is Insulin Resistant in the AD Presymptomatic Phase: Rescue by Nerve Growth Factor-Driven IRS1 Activation. Mol Neurobiol 56:535-552 (2019). PubMed: 29736736
- Kim HK et al. RRAD expression in gastric and colorectal cancer with peritoneal carcinomatosis. Sci Rep 9:19439 (2019). PubMed: 31857616
- Valentín-Guillama G et al. HIV-1 Envelope Protein gp120 Promotes Proliferation and the Activation of Glycolysis in Glioma Cell. Cancers (Basel) 10:N/A (2018). PubMed: 30200472