Anti-IDH1-R132P Mutant antibody (STJA0033621)

SPECIFICATIONS
ClonalityMonoclonal
HostMouse
ConjugationUnconjugated
IsotypeIgG
ImmunogenA synthetic peptide from the internal region of IDH1 which includes the mutation of R132P, human origin.
STJA0033621
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General Information

Short DescriptionMouse monoclonal anti-IDH1-R132P Mutant for use in WB, IHC-P, ICC, IF and ELISA in Vertebrates samples. Datasheet included with dilution recommendations, and related reagents.
ApplicationsWB/IHC-P/ICC/IF/ELISA
HostMouse
ReactivityVertebrates
NoteSTRICTLY FOR FURTHER SCIENTIFIC RESEARCH USE ONLY (RUO). MUST NOT TO BE USED IN DIAGNOSTIC OR THERAPEUTIC APPLICATIONS.

Product Properties

ClonalityMonoclonal
IsotypeIgG
ConjugationUnconjugated
PurificationPurified from ascites
Dilution RangeWB-1:100-1:1000
IHC-P-1:50-1:100
ICC/IF-1:50-1:100
ELISA-1:1000-1:5000
FormulationLiquid in PBS (without Mg2+ and Ca2+) , pH 7.4, 150 mM NaCl, 50% glycerol
Storage InstructionStore at-20°C. Avoid freeze/thaw cycles.

Target Information

ImmunogenA synthetic peptide from the internal region of IDH1 which includes the mutation of R132P, human origin.

Additional Info

Background Isocitrate dehydrogenases (IDH) catalyze the oxidative decarboxylation of isocitrate to 2-oxoglutarate. Mutations affecting Arg-132 are tissue-specific, and suggest that this residue plays a unique role in the development of high-grade gliomas. Mutations of Arg-132 to Cys, His, Leu or Ser abolish magnesium binding and abolish the conversion of isocitrate to alpha-ketoglutarate. Instead, alpha-ketoglutarate is converted to R-2-hydroxyglutarate. Elevated levels of R-2-hydroxyglutarate are correlated with an elevated risk of malignant brain tumors.

Information sourced from Uniprot.org

Citations

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