GRHPR Rabbit pAb
- 产品详情
- 实验流程
Application
| WB, IHC-P, IHC-F, IF |
|---|---|
| Primary Accession | Q9UBQ7 |
| Other Accession | Q9UBQ7 |
| Host | Rabbit |
| Clonality | Polyclonal |
| Calculated MW | 35668 Da |
| Physical State | Liquid |
| Immunogen | KLH conjugated synthetic peptide derived from human GRHPR |
| Epitope Specificity | 51-150/328 |
| Isotype | IgG |
| Purity | affinity purified by Protein A |
| Buffer | 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol. |
| SIMILARITY | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family. |
| DISEASE | Defects in GRHPR are the cause of hyperoxaluria primary type 2 (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. |
| Important Note | This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. |
| Background Descriptions | 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. [provided by RefSeq, Jul 2008] |
| Gene ID | 9380 |
|---|---|
| Other Names | GLXR; GLYD; PH2; GRHPR_HUMAN; GRHPR; 1.1.1.79; 1.1.1.81; glyoxylate and hydroxypyruvate reductase; glyoxylate reductase/hydroxypyruvate reductase; glyoxylate reductase and hydroxypyruvate reductase; primary hyperoxaluria type 2 |
| Dilution | WB=1:500-2000,IHC-P=1:100-500,IHC-F=1:100-500,IF=1:100-500 |
| Storage | Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C. |
For Research Use Only. Not For Use In Diagnostic Procedures.
| Name | GRHPR |
|---|---|
| Synonyms | GLXR |
| Function | Enzyme with hydroxy-pyruvate reductase, glyoxylate reductase and D-glycerate dehydrogenase enzymatic activities. Reduces hydroxypyruvate to D-glycerate, glyoxylate to glycolate, oxidizes D- glycerate to hydroxypyruvate. |
| Tissue Location | Ubiquitous. Most abundantly expressed in the liver. |
Research Areas
Application Protocols
Provided below are standard protocols that you may find useful for product applications.
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Cat# AP97270
















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