For analysis of glucose in plasma, serum, and urine
Features
  • Measure glucose in plasma, serum, and urine
  • Assay 40 samples in duplicate
  • Assay Range: 2.5-25 mg/dl
  • Plate-based colorimetric measurement (500-520 nm)
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Glucose Colorimetric Assay Kit

Item No. 10009582

Technical Information
Origin
Plant/Armoracia rusticana
Shipping & Storage Information
Storage
-20°C
Shipping
Wet ice in continental US; may vary elsewhere
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    Cayman Chemical
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    Product Description

    Glucose, a monosaccharide (or simple sugar), is the most important carbohydrate in biology. Transported via the blood stream, it is the primary source of energy for the body’s cells. Glucose level is tightly regulated in the human body. Failure to maintain blood glucose in the normal range leads to conditions of persistently high (hyperglycemia) or low (hypoglycemia) blood sugar. Diabetes mellitus, characterized by persistent hyperglycemia, is the most prominent disease related to failure of blood sugar regulation. Cayman’s Glucose Colorimetric Assay Kit provides a simple, reproducible, and sensitive tool for assaying glucose in plasma, serum, and urine. The glucose assay uses the glucose oxidase-peroxide reaction for the determination of glucose concentrations. In this assay, glucose is oxidized to δ-gluconolactone with concomitant reduction of the flavin adenine dinucleotide (FAD)-dependent enzyme glucose oxidase. The reduced form of glucose oxidase is regenerated to its oxidized form by molecular oxygen to produce hydrogen peroxide. Finally, with horseradish peroxidase as a catalyst, hydrogen peroxide reacts with 3,5-dichloro-2-hydroxybenzenesulfonic acid and 4-aminoantipyrine to generate a pink dye with an optimal absorption at 514 nm.

    Needed but not supplied: Please download the kit booklet to verify if UltraPure Water (Milli-Q or equivalent) or any other components are needed for this assay.

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Citations

    Hood, J.E., Yesudasan, S., and Averett, R.D. Glucose concentration affects fibrin clot structure and morphology as evidenced by fluorescence imaging and molecular simulations. Clincal and Applied Thrombosis/Hemostasis 24(9S), 104S-116S (2018).

    Kumari, S., Khan, S., Gupta, S.C., et alMUC13 contributes to rewiring of glucose metabolism in pancreatic cancer. Oncogenesis 7:19, (2018).

    Mühlemann, M., Zdzieblo, D., Friedrich, A.W., et alAltered pancreatic islet morphology and function in SGLT1 knockout mice on a glucose-deficient, fat-enriched diet. Mol. Metab. 13, 67-76 (2018).

    Scalzo, R.L., Knaub, L.A., Hull, S.E., et alGlucagon-like peptide-1 receptor antagonism impairs basal excercise capacity and vascular adaptation to aerobic exercise training in rats. Physiol. Rep. 6(13), (2018).

    Lee, P.R., Johnson, T.P., Gnanapavan, S., et alProtease-activated receptor-1 activation by granzyme B causes neurotoxicity that is augmented by interleukin-. J. Neuroinflammation 14(1), 131 (2017).

    French, W.W., Dridi, S., Shouse, S.A., et alA high-protein diet reduces weight gain, decreases food intake, decreases liver fat deposition, and improves markers of muscle metabolism in obese zucker rats. Nutrients 9(6), E587 (2017).

    Bertinato, J., Lavergne, C., Rahimi, S., et alModerately low magnesium intake impairs growth of lean body mass in obese-prone and obese-resistant rats fed a hgih-energy diet. Nutrients 8(5), E253 (2016).

    Harris, K.L., Pulliam, S.R., Okoro, E., et alWestern diet enhances benzo(a)pyrene-induced colon tumorigenesis in a polyposis in rat coli (PIRC) rat model of colon cancer. Oncotarget 7(20), 28947-28960 (2016).

    Lu, H.-J., Tzeng, T.-F., Liou, S.-S., et alRuscogenin ameliorates experimental nonalcoholic steatohepatitis via suppressing lipogenesis and inflammatory pathway. Biomed. Res. Int. 652680 (2014).

    Tzeng, T.F., Liou, S.S., Chang, C.J., et alZerumbone, a natural cyclic sesquiterpene of Zingiber zerumbet Smith, attenuates nonalcoholic fatty liver disease in hamsters fed on high-fat diet. Evid. Based Complement. Alternat. Med 2013, 303061 (2013).