Highly Sensitive 8-OHdG Check ELISA kit - Cosmo Bio Co.,Ltd.

Antibodies

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Highly Sensitive 8-OHdG Check ELISA kit

Catalog No.: NNS-KOG-HS10E-EX
Size: 96WELL
Price: ¥102400
$1366
antigen/source: 8-OHdG/8-oxo-dG
catalog info: Catalog 2012-p110
Storage: 4C
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Measurement Range: 0.125 - 10 ng / mL
Purpose: This product is a 8-OHdG ELISA kit utilizing anti 8-OHdG monoclonal antibody (clone N45.1) which is highly specific for 8-OHdG. We provide two types of 8-OHdG ELISA kits with different assay range. Highly Sensitive 8-OHdG Check ELISA is suitable for urine, serum , tissue and cultured cells.
component: Antibody: X
Plate: X
Coating: X
Control: -
Standard: X
Labeling: X
Substrate: X
Others: X
1. 8-OHdG Microtiter Plate: Precoated with 8-OHdG (12 X 8wells, split type) 1 plate
2. Primary Antibody: Anti 8-OHdG antibody, powder. 1 vial
3. Primary Antibody Solution 1 vial (6 mL )
4. Secondary Antibody: HRP-anti mouse antibody, powder. 1 vial
5. Secondary Antibody Solution: 1 vial (12 mL )
6. Chromatic Solution: 3,3',5,5'-tetramethylbenzidine 1 vial (0.25 mL )
7. Diluting Solution: H2O2 containing buffer. 1 vial (12 mL )
8. Washing Solution (5x): 2 vials (26 mL x 2)
9. Reaction Terminating Solution: 1M Phosphoric acid. 1 vial (12 mL )
10. Standard 8-OHdG Solution: Purified 8-OHdG (0.125, 0.25, 0.5, 1, 4, 10 ng / mL ) 1 vial each
11. Plate Seal: 2 sheets

Other:

 Supplementary 
Competitive
 Applicable sample 
Serum, Urine, Tissue, Cultured cells
[Other]
8-hydroxy-2'-deoxyguanosine (8-OHdG) is a product of oxidatively damaged DNA formed by hydroxy radical, singlet oxygen and direct photodynamic action. 8-OHdG can be detected in tissue, serum, urine and other biomaterials. New 8-OHdG Check is a competitive enzyme-linked immunosorbent assay (ELISA) utilising monoclonal antibody (clone N45.1) which is highly specific for DNA damage, not cross react with RNA oxidation products such as 8-hydroxy-guanine and 8-hydroxy-guanosine. This product is suitable for detection of 8-OHdG in urine and other biomaterialsfrom human and animals.



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Reference:

•  White, E. L. et al., J. Virol. Methods 70: 113-115 (1998)
◊  Neuroscience. 2010 Sep 29;170(1):337-47
◊  Cancer Prevention Research, 2010 Jul. 6: 686 - 694
 
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