DR1001
Anti-8-Hydroxyguanosine Goat pAb
liquid, Calbiochem®
Synonym(s):
Anti-8-OHG, Anti-8-oxo-G
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About This Item
UNSPSC Code:
12352203
biological source
goat
Quality Level
antibody form
serum
antibody product type
primary antibodies
clone
polyclonal
form
liquid
does not contain
preservative
species reactivity (predicted by homology)
all
manufacturer/tradename
Calbiochem®
storage condition
OK to freeze
avoid repeated freeze/thaw cycles
isotype
IgG
shipped in
wet ice
storage temp.
−20°C
target post-translational modification
unmodified
General description
Goat polyclonal antibody supplied as undiluted serum. Recognizes 8-hydroxydeoxy-guanosine.
Recognizes 8-Hydroxydeoxyguanosine in Alzheimer′s disease brain tissue.
This Anti-8-Hydroxyguanosine Goat polyclonal antibody detects 8-Hydroxydeoxyguanosine in Alzheimer′s disease brain tissue. It is validated for use in ELISA and with paraffin sections.
Immunogen
8-Hydroxyguanosine
Application
ELISA (≥1:250,000)
Paraffin Sections (≥1:200, proteinase K pre-treatment recommended; see figure legend, see application references)
Warning
Toxicity: Standard Handling (A)
Physical form
Undiluted serum.
Reconstitution
Following initial thaw, aliquot and freeze (-20°C).
Analysis Note
Positive Control
Alzheimer’s disease brain tissue
Alzheimer’s disease brain tissue
Other Notes
Abe, T., et al. 2003. Neurosci. Lett.336, 105.
Parker, A.R., et al. 2002. Cancer Res.62, 7230.
Parker, A.R., et al. 2002. Cancer Res.62, 7230.
Does not cross-react with other naturally occurring nucleotides. Antibody should be titrated for optimal results in individual systems.
Legal Information
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany
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Storage Class Code
10 - Combustible liquids
WGK
WGK 1
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Certificates of Analysis (COA)
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N Gueven et al.
Cell death and differentiation, 14(6), 1149-1161 (2007-03-10)
Several different autosomal recessive genetic disorders characterized by ataxia with oculomotor apraxia (AOA) have been identified with the unifying feature of defective DNA damage recognition and/or repair. We describe here the characterization of a novel form of AOA showing increased
Joseph J Boyle et al.
The American journal of pathology, 174(3), 1097-1108 (2009-02-24)
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