|
| |
| Cat. No |
Model |
Description |
Unit |
Price
(VAT별도) |
납기 |
재고 |
DataSheet |
주문/견적 |
| LCA-24-366940 |
AM03160PU-S |
8-Hydroxy-Guanosine (8-OHG)// |
1/EA |
|
|
|
 |
문의 |
|
|
|
|
|
|
|
Subject
|
8-Hydroxy-Guanosine (8-OHG) |
|
Description
|
/ |
|
Clonality
|
Mono |
|
Company
|
Acris Antibodies GmbH |
|
Application
|
Frozen sections, Enzyme Immunoassay |
|
Conjugation
|
|
|
Immunogen
|
|
|
Contents
|
Description: | Manufacturer | Acris Antibodies GmbH | | Quantity | 25 ug | | Presentation | Purified | | Applications | Frozen sections, Enzyme Immunoassay | | Isotype | IgG2a | | Host | Mouse | | Clone | 15A3 | | PDF datasheet | view | | Shipping to | Worldwide | | Synonyms | 8OHdG, 8-OFdG, 8OHG, 8-OHG, 8-Hydroxyguanosine, 8-Hydroxy-2\'-deoxyguanosine, 8-Hydroxyguanine, 8OG | | Immunogen | 8-hydroxy-guanosine-BSA and u“casein conjugates | | Product Type | Antibodies | | Recommended Isotype Control | AM03096PU-N | | Storage | Store the antibody at 2 - 8 °C up to one month or (in aliquots) at -20 °C for longer. Avoid repeated freezing and thawing. Shelf life: one year from despatch. | | References | 1. Kim H.W., Murakami A., Williams M.V., and Ohigashi H. (2003) Carcinogenesis 24(2): 235-241. 2. Pilger A. and Rudiger H.W. (2006) Int Arch Occup Environ Health. 80(1): 1-15. 3. Malins D.C. and Haimanot R. (1991) Cancer Res. 51(19): 5430-5432. 4. Kvam E. and Tyrrell R.M. (1997) Carcinogenesis 18(11): 2281-2283. 5. Kowluru R.A., Atasi L., and Ho Y.S. (2006) Invest Ophthalmol Vis Sci 47(4): 1594-9. 6. Bowers R. et al. (2004) Am J Respir Crit Care Med. 169(6): 764-9. 7. Cui J., Holmes E.H., Greene T.G., and Liu P.K. (2000) Faseb J. 14(7): 955-67. | |
| Format | State: Liquid Ig fraction | | ? | Purification: Protein G affinity chromatography | | ? | Buffer System: TBS, in 50 % glycerol, 0.09 % sodium azide | |
| Specificity | Recognizes markers of oxidative damage to DNA (8-hydroxy-2'-deoxyguanosine, 8-hydroxyguanine and 8-hydroxyguanosine). | | Application | ELISA. Immunohistochemistry on frozen secrtions. | | Background | DNA or RNA damage is due to environmental factors and normal metabolic processes inside the cell, that then hinder the ability of the cell to carry out its functions. There are four main types of DNA due to endogenous cellular processes and they are oxidation, alkylation, hydrolysis and mismatch of the bases. During the oxidation of bases, highly reactive chemical entities collectively known as RONS, occurs. RONS stands for reactive oxygen and nitrogen species and includes nitric oxide, superoxide, hydroxyl radical, hydrogen peroxide and peroxynitrite. Numerous studies have shown that RONS causes a variety of issues including DNA damage (1). 8-hydroxyguanine, 8-hydroxy-2u™-deoxyguanonsine and 8-hydroxyguanosine are all RNA and DNA markers of oxidative damage. 8-hydroxy-2u™-guanosine is produced by reactive oxygen and nitrogen species including hydroxyl radical and peroxynitrite. Specifically its high biological relevance is due to its ability to induce G to T transversions, which is one of the most frequent somatic mutations (2). 8-hydroxy-guanine has been the most frequently studied type of DNA base damage, with studies in diabetes, and cancer. Base modifications of this type arise from radical-induced hydroxylation and cleavage reactions of the purine ring (3, 4). And finally, 8-hydroxy-guanosine, like 8-hydroxy-2u™-guanosine, induces a mutagenic transversion of G to T in DNA. Its role has specifically been tested in the development of diabetes, hypertension and strokes (5, 6, and 7). | | Concentration | 0.65 mg/ml | |
|
|
|
|
