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    glucose-uptake-assay-kit-colorimetric-ab136955.pdf

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Signal Transduction Metabolism Energy Metabolism
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Glucose Uptake Assay Kit (Colorimetric) (ab136955)

  • Datasheet
  • SDS
  • Protocol Booklet
Reviews (1)Q&A (11)References (82)

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Standard curve and example data.
  • Functional Studies - Glucose Uptake Assay Kit (ab136955)
  • Assay Procedure

Key features and details

  • Assay type: Cell-based (quantitative)
  • Detection method: Colorimetric
  • Platform: Microplate reader
  • Assay time: 3 hr
  • Sample type: Adherent cells, Suspension cells
  • Sensitivity: 0.01 nmol/well

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Overview

  • Product name

    Glucose Uptake Assay Kit (Colorimetric)
    See all Glucose uptake kits
  • Detection method

    Colorimetric
  • Sample type

    Adherent cells, Suspension cells
  • Assay type

    Cell-based (quantitative)
  • Sensitivity

    <= 0.01 nmol/well
  • Assay time

    3h 00m
  • Species reactivity

    Reacts with: Mammals, Other species
  • Product overview

    Glucose Uptake Assay Kit (Colorimetric) (ab136955) is a highly sensitive and easy to use non-radioactive assay kit which can detect glucose uptake as low as 10 pmol/well in a variety of cell types.


    2-deoxyglucose (2-DG) is used in glucose uptake assay protocols because of its structural similarity to glucose. 2-DG is taken up by glucose transporters and metabolized to 2-DG-6-phosphate (2-DG6P). 2-DG6P cannot be further metabolized, and thus accumulates within cells. The accumulated 2-DG6P is directly proportional to 2-DG (or glucose) uptake by cells. In this assay, the 2-DG6P is oxidized to generate NADPH, the level of which can be determined by an enzymatic recycling amplification reaction.


    Glucose uptake assay protocol summary:
    - prepare cells with suitable glucose starvation / uptake stimulation depending on experimental set-up
    - add 2-DG to cells and incubate for 20 mins at 37ºC
    - wash cells with PBS to remove exogenous 2-DG
    - lyse cells with extraction buffer and repeated pipetting
    - freeze/thaw lysates and heat at 85ºC for 40 min
    - cool on ice for 5 min
    - add neutralizing buffer, spin and transfer supernatant to new tubes
    - add supernatants and standards to wells
    - add reaction mix A and incubate for 1 hr at 37ºC
    - add extraction buffer and heat to 90ºC for 40 min
    - cool on ice for 5 min and add neutralizing buffer
    - add reaction mix B
    - analyze every 2-3 mins on microplate reader in kinetic mode at 37ºC

  • Notes

    This product is manufactured by BioVision, an Abcam company and was previously called K676 Glucose Uptake Colorimetric Assay Kit. K676-100 is the same size as the 100 test size of ab136955.

    Review our Metabolism Assay Guide to learn about assays for metabolites, metabolic enzymes, mitochondrial function, and oxidative stress, and also about how to assay metabolic function in live cells using your plate reader.

  • Platform

    Microplate reader

Properties

  • Storage instructions

    Store at -20°C. Please refer to protocols.
  • Components Identifier 100 tests
    2-Deoxyglucose Purple 1 x 1ml
    2-DG6P Standard (Lyophilized) Yellow 1 vial
    Assay Buffer WM 1 x 25ml
    Enzyme Mix (Lyophilized) Orange 1 vial
    Extraction Buffer NM 1 x 17ml
    Glutathione Reductase (Lyophilized) Green 2 vials
    Neutralizing Buffer Clear 1 x 2.5ml
    Recycling Mix(Lyophilized) Blue 1 vial
    Substrate Red 2 vials
  • Research areas

    • Signal Transduction
    • Metabolism
    • Energy Metabolism
    • Kits/ Lysates/ Other
    • Kits
    • Cell Metabolism Kits
    • Sugar Assays
    • Metabolism
    • Pathways and Processes
    • Metabolic signaling pathways
    • Energy transfer pathways
    • Energy Metabolism

Associated products

  • Related Products

    • Glucose Uptake Assay Kit (Fluorometric) (ab136956)

Images

  • Standard curve and example data.
    Standard curve and example data.
    2-DG6P Standard curve (a) and 2-DG uptake in 3T3-L1 cells (b), Human adipocytes (c) and HeLa cells (d) respectively. I=Insulin; P=Phloretin.
  • Functional Studies - Glucose Uptake Assay Kit (ab136955)
    Functional Studies - Glucose Uptake Assay Kit (ab136955)

    Glucose uptake in 3T3-L1 adipocytes stimulated with insulin (I). 3T3-L1 adipocytes were differentiated using:

     

    Dexamethasone ab120743 (1mM, 1:1000)

    IBMX ab120840 (11.5 mg/mL, 1:100)

    Insulin ab123768 (1 mg/mL, 1:1000)

  • Assay Procedure
    Assay Procedure
    Step A: 2-DG oxidation to generate NADPH; Step B: NADPH recycling amplification Reaction.

Protocols

  • Protocol Booklet

Click here to view the general protocols

Datasheets and documents

  • SDS download

  • Datasheet download

    Download

References (82)

Publishing research using ab136955? Please let us know so that we can cite the reference in this datasheet.

ab136955 has been referenced in 82 publications.

  • Geberhiwot T  et al. Relative Adipose Tissue Failure in Alström Syndrome Drives Obesity-Induced Insulin Resistance. Diabetes 70:364-376 (2021). PubMed: 32994277
  • Jin X  et al. Long non-coding RNA MSC-AS1 facilitates the proliferation and glycolysis of gastric cancer cells by regulating PFKFB3 expression. Int J Med Sci 18:546-554 (2021). PubMed: 33390824
  • Obaid M  et al. LncRNA HOTAIR regulates glucose transporter Glut1 expression and glucose uptake in macrophages during inflammation. Sci Rep 11:232 (2021). PubMed: 33420270
  • Lee IK  et al. PEG-BHD1028 Peptide Regulates Insulin Resistance and Fatty Acid ß-Oxidation, and Mitochondrial Biogenesis by Binding to Two Heterogeneous Binding Sites of Adiponectin Receptors, AdipoR1 and AdipoR2. Int J Mol Sci 22:N/A (2021). PubMed: 33477324
  • Yang F  et al. LACTB induced apoptosis of oxaliplatin-resistant gastric cancer through regulating autophagy-mediated mitochondrial apoptosis pathway. Am J Transl Res 13:601-616 (2021). PubMed: 33594312
View all Publications for this product

Customer reviews and Q&As

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11-12 of 12 Abreviews or Q&A

Question

When you say " resuspend the cells in extraction buffer and transfer to an eppendorf tube " since MEFs adhere to the plate, how does the re-suspension actually work? does the extraction buffer have trypsin in it or some other compound that detaches the cell?

Read More

Abcam community

Verified customer

Asked on Feb 28 2013

Answer

We would recommend that you simply scrape the cells in the extraction buffer and take them out in eppendorf tubes. The heat/cool cycle will then take care of denaturing of enzymes.

Read More

Abcam Scientific Support

Answered on Feb 28 2013

Question

Do you culture cells in a special type of 96 well plates and perform the lysis in the 96 well plate themselves and does adding just the extraction buffer complete the lysis or do we require sonication?

I was also wondering, when you say add 1-50 ul sample per well do you mean we use another 96 well plate to do the actual assay and the first 96 well plate is just for preparation of the cultures and sample?

Read More

Abcam community

Verified customer

Asked on Feb 27 2013

Answer

When you are lysing the cells with the extraction buffer after treatment, you resuspend the cells in the buffer and then take them into other eppendorf tubes. You then perform the freeze thaw on them to efficiently lyse them. This is followed by heating, cooling and neutralization. Then you spin it down and take the supernatant in another 96 well plate in which you would perform the assay.

Read More

Abcam Scientific Support

Answered on Feb 27 2013

11-12 of 12 Abreviews or Q&A

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