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company name :
MyBioSource
product type :
other
product name :
OxiSelect In Vitro ROS/RNS Assay Kit (Green Fluorescence)
catalog :
MBS168257
quantity :
20 Assays
price :
325 USD
more info or order :
image
image 1 :
MyBioSource MBS168257 image 1
image 2 :
MyBioSource MBS168257 image 2
product information
catalog number :
MBS168257
products type :
Assay Kit
products full name :
OxiSelect In Vitro ROS/RNS Assay Kit (Green Fluorescence)
products short name :
[OxiSelect In Vitro ROS/RNS]
storage stability :
Upon receipt, store the DCF-DiOxyQ and DCF Standard at -20 degree C. Avoid multiple freeze/thaw cycles. Store all other components at 4 degree C.
image1 heading :
Testing Data
image2 heading :
Testing Data #2
products categories :
Oxidative Stress/ Damage; Reactive Oxygen Species (ROS) Assays; In Vitro ROS/RNS Assay
products description :
Principle of the Assay: The OxiSelect Ferric Reducing Antioxidant Power (FRAP) Assay Kit is a quantitative assay for measuring the antioxidant potential within a sample. Ferric iron (Fe3+) is initially reduced by electron-donating antioxidants present within the sample to its ferrous form (Fe2+). The iron-colorimetric probe complex develops a dark blue color product upon reduction which can be measured at 540-600 nm (see Figure 1). Samples can be compared to the iron standard for determining antioxidant potential. This assay is analytically sensitive to approximately 2 uM of Fe2+ iron equivalents, or a FRAP value of 2!!Background/Introduction: Oxidative stress is a physiological condition where there is an imbalance between concentrations of reactive oxygen species (ROS) and antioxidants. However, excessive ROS accumulation will lead to inflammation and cellular injury, such as damage to DNA, proteins, and lipid membranes. The cellular damage caused by ROS has been implicated in the development of many disease states, such as cancer, diabetes, cardiovascular disease, atherosclerosis, and neurodegenerative diseases. Under normal physiological conditions, cellular ROS generation is counterbalanced by the action of cellular antioxidant enzymes, macro or micro molecules, as well as other redox molecules. Antioxidants are molecules that contain one or more free electrons that can be donated to stabilize ROS. Antioxidants include both hydrophilic and lipophilic molecules for metabolizing ROS. These may be localized transiently within different tissues or cells. Because of their potential harmful effects, excessive ROS must be promptly neutralized and eliminated from the cells by this variety of antioxidant defense mechanisms. ???????????????????? OxiSelect Ferric Reducing Antioxidant Power (FRAP) Assay Kit is a quantitative assay for measuring the antioxidant potential within various samples such as serum, plasma, urine, saliva, tears, tissue homogenates, cell extracts, and purified food or drug extracts. The assay is based on the highly-cited work of Benzie and Strain (ref. 1 and 2) in which iron reacts with a colorimetric probe to produce a blue product. The reaction is driven by the electron donating reducing power of antioxidants. The kit employs a ferrous iron standard which allows the user to determine the antioxidant content present within their sample. Each kit provides sufficient reagents to perform up to 200 assays, including standard curve and unknown samples. The FRAP assay offers a simple and efficient analytical method for assessing age, disease, diet, or other physiological changes to antioxidant status.
products references :
1. Bass DA, Parce JW, Dechatelet LR, Szejda P, Seeds MC, Thomas M. Flow cytometric studies of oxidative product formation by neutrophils: A graded response to membrane stimulation. J Immunol. 1983; 130:1910-1917. 2. Brandt R, Keston AS. Synthesis of diacetyldichlorofluorescin: A stable reagent for fluorometric analysis. Anal Biochem. 1965; 11:6-9. 3. Keston AS, Brandt R. The fluorometric analysis of ultramicro quantities of hydrogen peroxide. Anal Biochem.1965; 11:1-5. 1. Schmidt-Heydt, M. et al. (2015). Oxidative stress induces the biosynthesis of citrinin by penicillium verrucosum at the expense of ochratoxin. Int J Food Microbiol. 192:1-6. 2. Khadir, A. et al. (2015). MAP kinase phosphatase DUSP1 is overexpressed in obese humans and modulated by physical exercise. Am J Physiol Endocrinol Metab. 308:E71-E83. 3. Ravassa, S. et al. (2015). Association of low GLP-1 with oxidative stress is related to cardiac disease and outcome in patients with type 2 diabetes mellitus: a pilot study. Free Radic Biol Med. doi: 10.1016/j.freeradbiomed.2015.01.002. 4. Canivet, L. et al. (2015). Effects of engineered iron nanoparticles on the bryophyte, Physcomitrella patens (Hedw.) Bruch & Schimp, after foliar exposure. Ecotoxicol Environ Saf. 113:499-505. 5. Meenalochani, S. et al. (2015). Sphingosine kinase 2 and sphingosine-1-phosphate promotes mitochondrial function in dopaminergic neurons of mouse model of Parkinson's Disease and in MPP+-treated MN9D cells in vitro. Neuroscience. doi: 10.1016/j.neuroscience.2015.01.032. 6. Walsh, C. J. et al. (2015). Sublethal red tide toxin exposure in free-ranging manatees (Trichechus manatus) affects the immune system through reduced lymphocyte proliferation responses, inflammation, and oxidative stress. Aquatic Toxicology. 161:73-84. 7. Rhyu, H. S. et al. (2014). The effects of ketogenic diet on oxidative stress and antioxidative capacity markers of Taekwondo athletes. J Exerc Rehabil. 10:362-366. 8. Hao, Y. et al. (2014). Mycoplasma pneumoniae modulates STAT3-STAT6/EGFR-FOXA2 signaling to induce overexpression of airway mucins. Infect Immun. 82:5246-5255. 9. Pandey, D. et al. (2014). Transcriptional regulation of endothelial arginase 2 by histone deacetylase 2. Arterioscler Thromb Vasc Biol. 34:1556-1566. 10. Liu, X. et al. (2013). Epoxyeicosatrienoic acids prevent cisplatin-induced renal apoptosis through a p38 mitogen-activated protein kinase-regulated mitochondrial pathway. Mol. Pharmacol. 84:925-934. 11. Song, J. et al. (2013). Nicotinamide phosphoribosyltransferase is required for the calorie restriction-mediated improvements in oxidative stress, mitochondrial biogenesis, and metabolic adaptation. J. Gerontol A Biol Sci Med Sci. 10.1093/gerona/glt122. 12. Xiao, D. et al. (2013). Estrogen normalizes perinatal nicotine-induced hypertensive responses in adult female rat offspring. Hypertension. 61:1246-1254. 13. Wang, W. et al. (2012). Mono-(2-ethylhexyl) phthalate induces oxidative stress and inhibits growth of mouse ovarian antral follicles. Biol Reprod. 87:152. 14. Ju, D.J. et al. (2012). Ethyl pyruvate ameliorates albuminuria and glomerular injury in the animal model of diabetic nephropathy. Am J Physiol Renal Physiol. 302: F606-F613. 15. Momi, S. et al. (2012). Nitric oxide enhances the anti-inflammatory and anti-atherogenic activity of atorvastatin in a mouse model of accelerated atherosclerosis. Cardiovasc Res. 10.1093/cvr/cvs100. 16. Patterson, A.J. et al. (2011). Hypoxia-derived oxidative stress mediates epigenetic repression of pkc? gene in foetal rat hearts. Cardiovasc Res. 10.1093/cvr/cvr322. 17. Rathnasamy, G. et al. (2011). Iron and iron regulatory proteins in amoeboid microglial cells are linked to oligodendrocyte death in hypoxic neonatal rat periventricular white matter through production of proinflammatory cytokines and reactive oxygen/nitrogen species. J. Neurosci. 31:17982-17995.
size1 :
20 Assays
price1 :
325 USD
size2 :
96 Assays
price2 :
595
size3 :
5x96 Assays
price3 :
2315
more info or order :
company information
MyBioSource
P.O. Box 153308
San Diego, CA 92195-3308
sales@mybiosource.com
https://www.mybiosource.com
1-888-627-0165
headquarters: USA
MyBioSource, LLC was orginally founded in Vancouver by three enthusiastic scientists who are passionate about providing the world with the best reagents available. Together, they form a company with a big vision known as MyBioSource. MyBioSource is now located in San Diego, California, USA.

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