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          • ELISA Kits ›
          • DNA Damage ELISA Kits

          Invitrogen

          DNA Damage Competitive ELISA Kit

          5 References

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          Technical guide & protocol Tech Support
          Technical guide & protocol Tech Support
          Technical guide & protocol Tech Support
          DNA Damage Competitive ELISA Kit (EIADNAD)
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          DNA Damage Competitive ELISA Kit (EIADNAD)
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          DNA Damage Competitive ELISA Kit

          Competitive ELISA {{ $ctrl.currentElement.advancedVerification.fullName }} validation info. View more
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          DNA Damage Competitive ELISA Kit (EIADNAD)
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          ►

          Product Specifications

          Analytical sensitivity

          50.9 pg/mL

          Assay range

          62.6-8,000 pg/mL

          Sample type/volume

          Digested DNA
          50 µL
          Fecal Extract
          50 µL
          Plasma
          6.25 µL
          Saliva
          25 µL
          Serum
          6.25 µL
          Supernatant
          50 µL
          Urine
          12.5 µL

          Hands-on time

          1 hr 20 min

          Time-to-result

          2 hr 30 min

          Homogenous (no wash)

          No

          Interassay CV

          9.9%

          Intraassay CV

          9%

          Instrument

          Absorbance Microplate Reader

          Product size

          96 Tests

          Contents

          Pre-coated 96 well plate
          Standard
          Assay Diluent concentrate
          HRP-Conjugated Detection Antibody
          Wash Buffer
          Chromogen
          Stop Solution
          Adhesive Plate Covers

          Shipping conditions

          Wet ice

          Storage

          -20°C

          Protein name

          DNA Damage

          Species (tested)

          Chemical

          Assay kit format

          Competitive ELISA

          Detector antibody conjugate

          HRP

          Label or dye

          HRP

          About This Kit

          The DNA Damage ELISA quantitates PGFM in serum, plasma, saliva, urine, digested DNA, fecal extracts, or cell culture medium.

          Principle of the method

          The DNA Damage Competitive ELISA research-use-only kit detects all three oxidized guanine species; 8-hydroxy-2'- deoxyguanosine from DNA, 8-hydroxyguanosine from RNA, and 8-hydroxyguanine from digested DNA from DNA or RNA. These species may be present in serum, plasma, saliva, urine, dried fecal samples, and tissue culture media samples. An 8-hydroxy-2'-deoxyguanosine (8-OHdG) stock solution is provided to generate a standard curve for the assay and all samples should be read off the standard curve. Standards or diluted samples are pipetted into a clear microtiter plate coated with an antibody to capture rabbit antibodies. An 8-hydroxyguanosine conjugate is added to the standards and samples in the wells. The binding reaction is initiated by the addition of a peroxidase-labeled mouse monoclonal antibody to 8-hydroxy-2'-deoxyguanosine to each well. After a 1-hour incubation the plate is washed and substrate added. The substrate reacts with the peroxidase labeled antibody that has reacted with the bound conjugate. After a short incubation, the reaction is stopped and the intensity of the generated color is detected in a microtiter plate reader capable of measuring at 450 nm.

          Rigorous validation

          Each manufactured lot of this ELISA kit is quality tested for criteria such as sensitivity, specificity, precision, and lot-to-lot consistency. See manual for more information on validation.

          Target information

          Free radicals and other reactive species are constantly generated in vivo and cause oxidative damage to biomolecules, a process held in check only by the existence of multiple antioxidant and repair systems as well as the replacement of damaged nucleic acids, proteins, and lipids. Intracellular free radical species (ROS) are produced as a result of normal metabolism and extracellular forms are produced as a result of ultraviolet radiation or ionizing radiation. Cellular function may be interrupted or stopped if DNA damage corrupts the integrity of essential information contained in the genome. When individual bases are damaged, nonspecific DNA repair enzymes excise DNA lesions to release deoxynucleotides, and base specific repair glycosylases excise the corresponding base. Deoxynucleotides are enzymatically hydrolyzed to stable deoxynucleosides, and these repair products are transported through the blood and excreted in the urine. Damage to RNA is reflected in nucleoside adducts. Among numerous types of oxidative DNA damage, the formation of 8-hydroxy-2'-deoxyguanosine (8-OHdG) is a ubiquitous marker of oxidative stress. 8-OHdG is physiologically formed and enhanced by chemical carcinogens. During the repair of damaged DNA in vivo by exonucleases, the resulting 8-OHdG is excreted without further metabolism into urine. 8-Hydroxy-2'-deoxyguanosine (8-OHdG) is identical across all species.

          For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.

          Recommended Products

          IL-6 Human Matched Antibody Pair

          Because you are interested in IL-6 Human ELISA Kit.

          SIZE

          10 x 96 tests

          PRICE

          USD 400.00

          Cat # CHC1263

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          Performance Guarantee

          If an Invitrogen™ immunoassay doesn't perform as described on our website or datasheet,we'll replace the product at no cost to you, or provide you with a credit for a future purchase.*

          Learn more
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          We're here to help

          Get expert recommendations for common problems or connect directly with an on staff expert for technical assistance related to applications, equipment and general product use.

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