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>   首页   >   产品   >   一抗   >   代谢   >   GRHPR Antibody (monoclonal) (M01)   

GRHPR Antibody (monoclonal) (M01)

Mouse monoclonal antibody raised against a full length recombinant GRHPR.

     
  • 1 - GRHPR Antibody (monoclonal) (M01) AT2260a
    GRHPR monoclonal antibody (M01), clone 4E6-1F2 Western Blot analysis of GRHPR expression in MCF-7 ( Cat # L046V1 ).
  • 10 - GRHPR Antibody (monoclonal) (M01) AT2260a
    Detection limit for recombinant GST tagged GRHPR is approximately 0.03ng/ml as a capture antibody.
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Product Information
Application
  • Applications Legend:
  • E=ELISA
  • WB=Western Blotting
  • IHC=Immunohistochemistry
  • IHC-P=Immunohistochemistry (Paraffin)
  • IP=Immunoprecipitation
  • IF=Immunofluorescence
  • IC=Immunochemistry
  • ICC=Immunocytochemistry
  • FC=Flow Cytometry
  • DB=Dot Blot
WB, E
Primary Accession Q9UBQ7
Other Accession BC000605
Reactivity Human
Host Mouse
Clonality monoclonal
Isotype IgG1 Kappa
Clone Names 4E6-1F2
Calculated MW 35668 Da
Additional Information
Gene ID 9380
Other Names Glyoxylate reductase/hydroxypyruvate reductase, GRHPR, GLXR
Target/Specificity GRHPR (AAH00605, 1 a.a. ~ 328 a.a) full-length recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.
Dilution WB~~1:500~1000
E~~N/A
Format Clear, colorless solution in phosphate buffered saline, pH 7.2 .
StorageStore at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
PrecautionsGRHPR Antibody (monoclonal) (M01) is for research use only and not for use in diagnostic or therapeutic procedures.
Research Areas

For Research Use Only. Not For Use In Diagnostic Procedures.

BACKGROUND

This 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.

REFERENCES

Late diagnosis of primary hyperoxaluria type 2 in the adult: effect of a novel mutation in GRHPR gene on enzymatic activity and molecular modeling. Levin-Iaina N, et al. J Urol, 2009 May. PMID 19296982.A novel mutation in the GRHPR gene in a Japanese patient with primary hyperoxaluria type 2. Takayama T, et al. Nephrol Dial Transplant, 2007 Aug. PMID 17510093.Structural basis of substrate specificity in human glyoxylate reductase/hydroxypyruvate reductase. Booth MP, et al. J Mol Biol, 2006 Jun 30. PMID 16756993.The LIFEdb database in 2006. Mehrle A, et al. Nucleic Acids Res, 2006 Jan 1. PMID 16381901.Primary hyperoxaluria: from gene defects to designer drugs? Danpure CJ. Nephrol Dial Transplant, 2005 Aug. PMID 15956068.

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