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货号:DIGL-100    品牌:BioAssay Systems

生化分析试剂盒

名称:QuantiChrom™ Glucose Assay Kit 葡萄糖(化学法)测试盒
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品牌货号产品名称规格
BioAssay SystemsDIGL-100

QuantiChrom™ Glucose Assay Kit

葡萄糖(化学法)测试盒

100T

说明书:

DIGL.pdf


Application

  • For quantitative determination of glucose and evaluation of drug effects on glucose metabolism.

Key Features

  • Sensitive and accurate. Use as little as 5 μL samples. Linear detection range 0.7 mg/dL (39 μM) to 300 mg/dL (16.6 mM) glucose in 96-well plate.
  • Simple and convenient. The procedure involves addition of a single working reagent and incubation for 8 min in a boiling water bath.
  • Improved reagent stability. The optimized formulation has greatly enhanced the reagent and signal stability.
  • Low interference in biological samples. No pretreatments are needed. Assays can be directly performed on serum and plasma samples.

Method

  •  OD630nm (Chemical)

Samples

  •  Biological, food and beverage

Species

  •  All

Size

  •  100 tests

Detection Limit

  •  0.7 mg/dL (39 μM)

Shelf Life

  •  12 months

More Details

  •  Glucose (C6H12O6) is a ubiquitous fuel molecule in biology. It is oxidized through a series of enzyme-catalyzed reactions to form carbon dioxide and water, yielding the universal energy molecule ATP. Due to its importance in metabolism, glucose level is a key diagnostic parameter for many metabolic disorders. Increased glucose levels have been associated with diabetes mellitus, hyperactivity of thyroid, pituitary and adrenal glands. Decreased levels are found in insulin secreting tumors, myxedema, hypopituitarism and hypoadrenalism. Simple, direct and automation-ready procedures for measuring glucose concentrations find wide applications in research and drug discovery. BioAssay Systems glucose assay kit is designed to measure glucose directly in serum or plasma without any pretreatment. The improved o-toluidine method utilizes a specific color reaction with glucose. The absorbance at 630nm is directly proportional to glucose concentration in the sample.


·相关文献


Kazemi, M., McBreairty, L., Chizen, D., Pierson, R., Chilibeck, P., & Zello, G. (2018). A Comparison of a Pulse-Based Diet and the Therapeutic Lifestyle Changes Diet in Combination with Exercise and Health Counselling on the Cardio-Metabolic Risk Profile in Women with Polycystic Ovary Syndrome: A Randomized Controlled Trial. Nutrients, 10(10), 1387. Assay: Glucose in human plasma.

Amrithraj, A. I., Kodali, A., Nguyen, L., Teo, A. K. K., Chang, C. W., Karnani, N. & Stunkel, W. (2017). Gestational diabetes alters functions in offspring's umbilical cord cells with implications for cardiovascular health. Endocrinology, 158(7), 2102-2112. Assay: Glucose in human cells.

Chen, X., Xu, H., Wu, N., Liu, X., Qiao, G., Su, S. & Lin, X. (2017). Interaction between granulin A and enolase 1 attenuates the migration and invasion of human hepatoma cells. Oncotarget 8(18): 30305-30316. Assay: Glucose in human lung tissue/plasma.

McMurphy, T. B. (2017). Environmental and gene therapy approaches to improve glycemic control and promote healthy aging (Doctoral dissertation, The Ohio State University). Assay: Glucose in mice blood.

Toorie, A. M., Cyr, N. E., Steger, J. S., Beckman, R., Farah, G., & Nillni, E. A. (2016). The nutrient and energy sensor Sirt1 regulates the hypothalamic-pituitary-adrenal (HPA) axis by altering the production of the prohormone convertase 2 (PC2) essential in the maturation of corticotropin-releasing hormone (CRH) from its prohormone in male rats. Journal of Biological Chemistry, 291(11), 5844-5859. Assay: Glucose in Sprague Dewley rats plasma.

Chiu LL, Radisic M (2010). Scaffolds with covalently immobilized VEGF and Angiopoietin-1 for vascularization of engineered tissues. Biomaterials 31(2):226-41. Assay: Glucose in human endothelial cells.

Hedbacker, K et al (2010). Antidiabetic effects of IGFBP2, a leptin-regulated gene. Cell Metab. 11(1):11-22. Assay: Glucose in mouse blood.

Olsen AS, et al (2010). Limb regeneration is impaired in an adult zebrafish model of diabetes mellitus. Wound Repair Regen. 18(5):532-42. Assay: Glucose in zebrafish blood.

Vaitheesvaran B, et al (2010). MKR mice have increased dynamic glucose disposal despite metabolic inflexibility, and hepatic and peripheral insulin insensitivity. Diabetologia 53(10):2224-32. Assay: Glucose in mice serum.

Cirrik S, Oner G. (2009). The effect of heavy muscle activity on renal cytoresistance in rats. Ren Fail. 31(8):683-9. Assay: Glucose in rat urine.

Li, L et al (2009). The nuclear orphan receptor COUP-TFII plays an essential role in adipogenesis, glucose homeostasis, and energy metabolism. Cell Metab. 9(1):77-87. Assay: Glucose in mouse plasma.

Sekowska, A et al (2009). Repulsion and metabolic switches in the collective behavior of bacterial colonies. Biophys J. 97(3):688-98. Assay: Glucose in bacteria cell lysate.

Sullivan JP, et al (2008). Convection and hemoglobin-based oxygen carrier enhanced oxygen transport in a hepatic hollow fiber bioreactor. Artif Cells Blood Substit Immobil Biotechnol. 36(4):386-402. Assay: Glucose in bioreactors daily media.

Zheng Y, et al (2007). Evaluation of different biomass materials as feedstock for fermentable sugar production. Appl Biochem Biotechnol. 137-140(1-12):423-35. Assay: Glucose in wood enzyme.

Jatana M, et al (2006). Inhibition of NF-kappaB activation by 5-lipoxygenase inhibitors protects brain against injury in a rat model of focal cerebral ischemia. J Neuroinflammation 3:12. Assay: Glucose in rat plasma.

Stites T, et al (2006). Pyrroloquinoline quinone modulates mitochondrial quantity and function in mice. J Nutr. 136(2):390-6. Assay: Glucose in mice plasma.