HAO1 Monoclonal Antibody(Mix)
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Application
| WB, IHC-P, IF |
|---|---|
| Primary Accession | Q9UJM8 |
| Reactivity | Mouse, Rat |
| Host | Mouse |
| Clonality | Monoclonal |
| Calculated MW | 40924 Da |
| Gene ID | 54363 |
|---|---|
| Other Names | Hydroxyacid oxidase 1; HAOX1; Glycolate oxidase; GOX |
| Dilution | WB~~WB: 1:1000-2000 IF 1:200 IHC 1:50-300 IHC-P~~WB: 1:1000-2000 IF 1:200 IHC 1:50-300 IF~~1:50~200 |
| Format | PBS, pH 7.4, containing 0.09% (W/V) sodium azide as Preservative and 50% Glycerol. |
| Storage Conditions | -20℃ |
| Name | HAO1 {ECO:0000303|PubMed:10978532, ECO:0000312|HGNC:HGNC:4809} |
|---|---|
| Function | Broad substrate specificity (S)-2-hydroxy-acid oxidase that preferentially oxidizes glycolate (PubMed:10777549, PubMed:10978532, PubMed:17669354, PubMed:18215067). The glyoxylate produced by the oxidation of glycolate can then be utilized by alanine-glyoxylate aminotransferase for the peroxisomal synthesis of glycine; this pathway appears to be an important step for the detoxification of glyoxylate which, if allowed to accumulate, may be metabolized to oxalate with formation of kidney stones (PubMed:10978532, PubMed:17669354). Can also catalyze the oxidation of glyoxylate, and long chain hydroxyacids such as 2-hydroxyhexadecanoate and 2-hydroxyoctanoate, albeit with much lower catalytic efficiency (PubMed:10777549, PubMed:17669354, PubMed:18215067). Active in vitro with the artificial electron acceptor 2,6-dichlorophenolindophenol (DCIP), but O2 is believed to be the physiological electron acceptor, leading to the production of H2O2 (PubMed:10777549, PubMed:10978532, PubMed:17669354, PubMed:18215067). Is not active on L-lactate and 2-hydroxybutanoate (PubMed:10777549). |
| Cellular Location | Peroxisome matrix. |
| Tissue Location | Highly expressed in liver. |
Research Areas
For Research Use Only. Not For Use In Diagnostic Procedures.
Application Protocols
Provided below are standard protocols that you may find useful for product applications.
BACKGROUND
Has 2-hydroxyacid oxidase activity. Most active on the 2-carbon substrate glycolate, but is also active on 2-hydroxy fatty acids, with high activity towards 2-hydroxy palmitate and 2- hydroxy octanoate.
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