MAB3560-C
Anti-8-Oxoguanine, clone 483.15 Antibody (Ascites Free)
clone 483.15, from mouse
Synonym(s):
8-Oxoguanine
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About This Item
UNSPSC Code:
12352203
eCl@ss:
32160702
NACRES:
NA.41
Recommended Products
biological source
mouse
Quality Level
antibody form
purified immunoglobulin
antibody product type
primary antibodies
clone
483.15, monoclonal
species reactivity
rat, human, monkey, bovine, mouse
species reactivity (predicted by homology)
all
technique(s)
ELISA: suitable
immunocytochemistry: suitable
immunohistochemistry: suitable
isotype
IgMκ
shipped in
dry ice
target post-translational modification
unmodified
Gene Information
human ... OGG1(4968)
General description
8-Oxoguanine is a mutagenic oxidative damage product of guanine. Oxidatively damaged base 8-oxoguanine is generated in the DNA of all living organisms due to the presence of reactive oxygen species in cells. DNA damage threatens the health of the genetic information stored in every DNA molecule; however enzymes exist in cells to protect against the mutagenic effect of this lesion. 8-oxoguanine is one of the most abundant and well-characterized DNA lesions generated by oxidative stress. It has been estimated that ~180 guanines are oxidized to 8-oxoG per mammalian cell per day. 8-oxoG is a miscoding lesion that can cause G:C to T:A or T:A to G:C transversion mutations. This lesion accumulates in DNA with age and it has been loosly linked to several cancers and diseases, such as Alzheimer′s and Parkinson′s.
Specificity
8-oxoguanine. By competitive ELISA the monoclonal showed no reactivity with dGMP, dAMP, dCMP or TMP in micromolar concentrations. Competition was only observed when the concentrations were increased to the millimolar range.
Target DNA modification is not species-specific.
Immunogen
8-oxoguanine adsorbed on to alumina.
Application
Immunohistochemistry Analysis: A representative lot detected cells with 8-oxoguanine (8-oxoG) immunoreactivity in the central veins (CV) and portal triads (PT) regions of paraffin-embedded kettle liver sections (García-Vaquero, M., et al. (2012). Animal.6(9):1435-1443).
Immunohistochemistry Analysis: A representative lot detected increased nuclear 8-oxoguanine (8-oxoG) immunoreactivity in paraffin-embedded coronal hippocampus sections from mice induced to express mutated mitochondrial isoform Uracil–DNA glycosylase by fluorescent immunohistochemistry (Lauritzen, K.H., et al. (2011). DNA Repair (Amst). 10(6):639-653).
Immunohistochemistry Analysis: A representative lot detected significantly increased nuclear 8-oxoguanine (8-oxoG) immunoreactivity in ovaries excised from neonatal mice upon exposure to ovotoxic agent 4-vinylcyclohexene diepoxide (VCD), methoxychlor (MXC), or menadione (MEN) in culture by fluorescent immunohistochemistry (Sobinoff, A.P., et al. (2010). Toxicol. Sci. 118(2):653-666).
Immunocytochemistry Analysis: A representative lot detected significantly increased 8-oxoguanine (8-oxoG) immunoreactivity in RINm5F rat insulinoma cells upon IL-1beta or ROS-inducer menadione treatment (Mehmeti, I., et al. (2011). Biochim. Biophys. Acta. 1813(10):1827-1835).
Immunocytochemistry Analysis: A representative lot detected significantly increased nuclear 8-oxoguanine (8-oxoG) immunoreactivity in AC16 human cardiomyocytes upon infection by the hemoflagellate protozoan parasite Trypanosoma cruzi (Ba, X., et al. (2010). J. Biol. Chem. 285(15):11596-11606).
Immunocytochemistry Analysis: Representative lots detected nutrient-deprivation-induced enhancement of nuclear 8-oxoguanine (8-oxoG) immunoreactivity in HeLa and COS-7 cells by fluorescent immunocytochemistry (Conlon, K.A., et al. (2003). DNA Repair (Amst). 2(12):1337-1352; Conlon, K.A., et al. (2000). J. Histotechnol. 23(1):37-44).
ELISA Analysis: Specificity of a representative lot against 8-oxoguanine was confirmed by competitive ELISA. Competition by dGMP, dAMP, dCMP or TMP was only observed when the concentrations were increased to the millimolar range.
Immunohistochemistry Analysis: A representative lot detected increased nuclear 8-oxoguanine (8-oxoG) immunoreactivity in paraffin-embedded coronal hippocampus sections from mice induced to express mutated mitochondrial isoform Uracil–DNA glycosylase by fluorescent immunohistochemistry (Lauritzen, K.H., et al. (2011). DNA Repair (Amst). 10(6):639-653).
Immunohistochemistry Analysis: A representative lot detected significantly increased nuclear 8-oxoguanine (8-oxoG) immunoreactivity in ovaries excised from neonatal mice upon exposure to ovotoxic agent 4-vinylcyclohexene diepoxide (VCD), methoxychlor (MXC), or menadione (MEN) in culture by fluorescent immunohistochemistry (Sobinoff, A.P., et al. (2010). Toxicol. Sci. 118(2):653-666).
Immunocytochemistry Analysis: A representative lot detected significantly increased 8-oxoguanine (8-oxoG) immunoreactivity in RINm5F rat insulinoma cells upon IL-1beta or ROS-inducer menadione treatment (Mehmeti, I., et al. (2011). Biochim. Biophys. Acta. 1813(10):1827-1835).
Immunocytochemistry Analysis: A representative lot detected significantly increased nuclear 8-oxoguanine (8-oxoG) immunoreactivity in AC16 human cardiomyocytes upon infection by the hemoflagellate protozoan parasite Trypanosoma cruzi (Ba, X., et al. (2010). J. Biol. Chem. 285(15):11596-11606).
Immunocytochemistry Analysis: Representative lots detected nutrient-deprivation-induced enhancement of nuclear 8-oxoguanine (8-oxoG) immunoreactivity in HeLa and COS-7 cells by fluorescent immunocytochemistry (Conlon, K.A., et al. (2003). DNA Repair (Amst). 2(12):1337-1352; Conlon, K.A., et al. (2000). J. Histotechnol. 23(1):37-44).
ELISA Analysis: Specificity of a representative lot against 8-oxoguanine was confirmed by competitive ELISA. Competition by dGMP, dAMP, dCMP or TMP was only observed when the concentrations were increased to the millimolar range.
This Anti-8-Oxoguanine, clone 483.15 Antibody (Ascites Free) is validated for use in Immunocytochemistry, Immunohistochemistry and ELISA for the detection of 8-Oxoguanine.
Quality
Evaluated by Immunocytochemistry in HeLa cells.
Immunocytochemistry Analysis: A 1:50 dilution of this antibody detected 8-Oxoguanine in HeLa cells.
Immunocytochemistry Analysis: A 1:50 dilution of this antibody detected 8-Oxoguanine in HeLa cells.
Linkage
Replaces: MAB3560
Physical form
Format: Purified
Purified mouse monoclonal IgMκ antibody in PBS without preservatives (azide free).
Other Notes
Concentration: Please refer to lot specific datasheet.
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Storage Class Code
12 - Non Combustible Liquids
WGK
WGK 2
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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Knut H Lauritzen et al.
DNA repair, 10(6), 639-653 (2011-05-10)
Mitochondria are highly dynamic organelles that can be actively transported within the cell to satisfy local requirements. They are vital for providing cellular energy, but are also an important endogenous source of reactive oxygen species. The distribution of mitochondria is
Alexander P Sobinoff et al.
Toxicological sciences : an official journal of the Society of Toxicology, 118(2), 653-666 (2010-09-11)
Mammalian females are born with a finite number of nonrenewing primordial follicles, the majority of which remain in a quiescent state for many years. Because of their nonrenewing nature, these "resting" oocytes are particularly vulnerable to xenobiotic insult, resulting in
Immunofluorescent localization of the murine 8-oxoguanine DNA glycosylase (mOGG1) in cells growing under normal and nutrient deprivation conditions.
Conlon, KA; Zharkov, DO; Berrios, M
DNA Repair null
Ilir Mehmeti et al.
Biochimica et biophysica acta, 1813(10), 1827-1835 (2011-07-26)
Pro-inflammatory cytokine-mediated beta cell apoptosis is activated through multiple signaling pathways involving mitochondria and endoplasmic reticulum. Activation of organelle-specific caspases has been implicated in the progression and execution of cell death. This study was therefore performed to elucidate the effects
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Frontiers in plant science, 11, 596-596 (2020-06-09)
Maize shoot development progresses from non-pigmented meristematic cells at the base of the leaf to expanded and non-dividing green cells of the leaf blade. This transition is accompanied by the conversion of promitochondria and proplastids to their mature forms and
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