anti-Thymidine Glycol [TG], mAb (2E8)

CHF 595.00
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JAI-MTG-100P100 µgCHF 595.00
 
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Product Details
Product Type Monoclonal Antibody
Properties
Clone 2E8
Isotype Mouse IgG1κ
Immunogen/Antigen Thymidine glycol polymer.
Application Immunohistochemistry: Recommended concentration is 5-10μg/mL
Crossreactivity All
Human
Specificity Recognizes DNA containing thymidine glycol. Does not cross-react with oxidized dC polymer, oxidized dG polymer and oxidized dA polymer. Does not react with free thymidine glycol.
Formulation Lyophilized. Contains 10mM PBS, pH7.4 containing 1.0% BSA.
Reconstitution Reconstitute with 1mL distilled water.
Other Product Data Click here for Original Manufacturer Product Datasheet
Our product description may differ slightly from the original manufacturers product datasheet.
Declaration Manufactured by JaICA.
Shipping and Handling
Shipping BLUE ICE
Short Term Storage +4°C
Long Term Storage -20°C
Handling Advice Avoid freeze/thaw cycles.
Use/Stability Stable for at least 3 years after receipt when stored at -20°C.
After reconstitution, prepare aliquots and store at -20°C.
Documents
MSDS No
Product Specification Sheet
Datasheet Download PDF
Thymidineglycol (TG) is one of the major oxidation products of DNA. Thymidine (T) can be damaged by oxidative stress such as radiation and energy metabolism. Two different pathways to form TG have been suggested. Deoxythymidine in DNA is directly oxidised by hydroxy radical, to form TG. TG can be also formed through an intermediate thymidine chlorohydrin, which is derived from hypochlorous acid (HOCl) from neutrophil myeloperoxidase. Thymidineglycol is derived from DNA, not from RNA. TG is the oxidative stress marker secific for DNA damage. In comparison with 8-hydroxy-2'-deoxyguanosine (8-OHdG), which is the best known DNA oxidation product it was shown that in a lipopolysaccharide (LPS)-treated mouse liver, 8-OHdG can be stained within 24 hours after LPS treatment. TG can be detected within 6 hours, and remains at least for 72 hours.
Product References
  1. Serum antioxidant capacity and oxidative injury to pulmonary DNA in never-smokers with primary lung cancer: K. Ito, et al.; Anticancer Res. 32, 1063 (2012)
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