GRHPR rabbit pAb

GRHPR rabbit pAb

AO-06-ES15908-100

GRHPR rabbit pAb 100μL

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Antibody Product Overview

ELK.NoES15908
Product nameGRHPR rabbit pAb
ReactivityHuman; Mouse
ApplicationsWB
Other name
Size100μL
Unit price ($)248
Human gene ID9380
Human Swiss-ProtQ9UBQ7
SourceRabbit
IsotypeIgG
TargetGRHPR
Fields>>Glycine, serine and threonine metabolism;>>Pyruvate metabolism;>>Glyoxylate and dicarboxylate metabolism;>>Metabolic pathways
Gene nameGRHPR GLXR MSTP035
Protein nameGRHPR
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID76238
Mouse gene linkView Mouse Gene
Mouse Swiss-ProtQ91Z53
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID
Rat gene link
Rat Swiss-Prot
Rat Swiss link
ImmunogenSynthesized peptide derived from human GRHPR AA range: 151-201
SpecificityThis antibody detects endogenous levels of GRHPR at Human/Mouse
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWB 1:500-2000
PurificationThe antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)36kD
Observed band (KD)
BackgroundThis gene encodes an enzyme with hydroxypyruvate reductase, glyoxylate reductase, and D-glycerate dehydrogenase enzymatic activities. The enzyme has widespread tissue expression and has a role in metabolism. Type II hyperoxaluria is caused by mutations in this gene. [provided by RefSeq, Jul 2008],
Functioncatalytic activity:Glycolate + NADP(+) = glyoxylate + NADPH.,disease:Defects in GRHPR are the cause of hyperoxaluria primary type II (HP2) [MIM:260000]; also known as primary hyperoxaluria type II (PH2). HP2 is a disorder where the main clinical manifestation is calcium oxalate nephrolithiasis though chronic as well as terminal renal insufficiency has been described. It is characterized by an elevated urinary excretion of oxalate and L-glycerate.,function:Enzyme with hydroxy-pyruvate reductase, glyoxylate reductase and D-glycerate dehydrogenase enzymatic activities.,similarity:Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family.,subunit:Monomer.,tissue specificity:Ubiquitous. Most abundantly expressed in the liver.,
Subcellular locationcytoplasm,peroxisomal matrix,cytosol,extracellular exosome,
ExpressionUbiquitous. Most abundantly expressed in the liver.

Additional Images

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Western blot analysis of lysates from Jarkat cells, primary antibody was diluted at 1:1000, 4°over night
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: AO-06-ES15908-100
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Hurry! only 10 items left in stock.

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