Recombinant Mouse Acox3 protein, His & T7-tagged
Cat.No. : | Acox3-8163M |
Product Overview : | Recombinant Mouse Acox3 aa. (Ser529~Leu700 (Accession # Q9EPL9)) fused with N-terminal His & T7 tag was produced in E. coli cells. |
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Source : | E. coli |
Species : | Mouse |
Tag : | His & T7 |
Form : | Freeze-dried powder |
Molecular Mass : | Predicted Molecular Mass: 23.0kDa. |
Protein length : | Ser529~Leu700 (Accession # Q9EPL9) |
Endotoxin : | <1.0EU per 1ug (determined by the LAL method) |
Purity : | >90% |
Characteristic : | The isoelectric point is 7.7. |
Applications : | SDS-PAGE; WB; ELISA; IP. |
Stability : | The thermal stability is described by the loss rate of the target protein. The loss rate was determined by accelerated thermal degradation test, that is, incubate the protein at 37°C for 48h, and no obvious degradation and precipitation were observed. (Referring from China Biological Products Standard, which was calculated by the Arrhenius equation.) The loss of this protein is less than 5% within the expiration date under appropriate storage condition. |
Storage : | Avoid repeated freeze/thaw cycles. Store at 2-8°C for one month. Aliquot and store at -80°C for 12 months. |
Storage Buffer : | Supplied as lyophilized form in 20mM Tris, 150mM NaCl, pH8.0, containing 1mM EDTA, 1mM DTT, 0.01% sarcosyl, 5% trehalose, and preservative. |
Reconstitution : | Reconstitute in sterile ddH2O. |
Gene Name : | Acox3 acyl-Coenzyme A oxidase 3, pristanoyl [ Mus musculus (house mouse) ] |
Official Symbol : | Acox3 |
Synonyms : | Acox3; acyl-Coenzyme A oxidase 3, pristanoyl; PCOX; EST-s59; BI685180; peroxisomal acyl-coenzyme A oxidase 3; BRCACox; branched-chain acyl-CoA oxidase; pristanoyl-CoA oxidase |
Gene ID : | 80911 |
mRNA Refseq : | NM_030721.2 |
Protein Refseq : | NP_109646.2 |
UniProt ID : | Q9EPL9 |
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For Research Use Only. Not intended for any clinical use. No products from Creative BioMart may be resold, modified for resale or used to manufacture commercial products without prior written approval from Creative BioMart.
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Q&As (15)
Ask a questionACOX3 protein levels and activity have been shown to be altered in various metabolic disorders, such as X-ALD and non-alcoholic fatty liver disease (NAFLD), suggesting that it could be a potential biomarker for these conditions.
There are currently no drugs that specifically target ACOX3, but certain drugs used to treat metabolic disorders, such as bezafibrate and gemfibrozil, have been shown to stimulate the activity of ACOX3 and other fatty acid oxidation enzymes.
Mutations in the ACOX3 gene have been associated with certain peroxisomal disorders, such as X-linked adrenoleukodystrophy (X-ALD). These mutations can result in a decrease in ACOX3 activity, leading to the accumulation of VLCFAs and other metabolites that contribute to disease pathology.
ACOX3 has been used in biotechnology applications such as the production of long-chain fatty alcohols and alkanes for use as biofuels. Expression of ACOX3 can increase the production of these compounds in microbes such as E. coli.
ACOX3 expression and activity are regulated by a variety of factors, including peroxisome proliferator-activated receptor (PPAR) alpha, which is a key regulator of fatty acid oxidation. ACOX3 expression is also influenced by various signaling pathways and transcription factors, such as the sterol regulatory element-binding protein (SREBP) pathway.
There is limited research on the potential use of ACOX3 protein to improve athletic performance. While ACOX3 is involved in fatty acid oxidation, which is a major energy source for endurance exercise, further studies are needed to determine its potential as a performance-enhancing substance.
ACOX3 protein levels have been shown to be altered in certain diseases such as peroxisomal disorders, suggesting its potential as a diagnostic marker for these conditions. However, further studies are needed to determine the diagnostic utility of ACOX3 in clinical settings.
ACOX3 has been identified as a potential therapeutic target for metabolic disorders, particularly X-ALD. However, further research is needed to develop targeted therapies.
ACOX3 works in concert with other enzymes involved in fatty acid metabolism, including carnitine palmitoyltransferase (CPT) and acyl-CoA dehydrogenase (ACAD). CPT transfers fatty acids into the mitochondria for oxidation, while ACAD is responsible for the initial step in beta-oxidation.
Certain dietary interventions, such as fasting and the consumption of medium-chain triglycerides (MCTs), have been shown to increase ACOX3 activity and fatty acid oxidation in the liver.
In addition to its role in the oxidation of VLCFAs, ACOX3 has also been shown to play a role in the synthesis of certain lipids, such as sphingolipids and plasmalogens. These lipids have important functions in cellular membranes and signaling pathways.
The role of ACOX3 in cancer development is not well understood. Some studies have suggested that ACOX3 expression is decreased in certain types of cancer, such as bladder cancer, while others have shown increased expression in breast cancer. More research is needed to determine the potential role of ACOX3 in cancer development and progression.
ACOX3 has been suggested as a potential target for drug development in a variety of metabolic disorders, including peroxisomal disorders and nonalcoholic fatty liver disease (NAFLD). Inhibition of ACOX3 activity has been shown to reduce the accumulation of VLCFA, which can contribute to disease pathology.
ACOX3 expression has been shown to be altered in certain metabolic disorders such as peroxisomal disorders and NAFLD, suggesting its potential as a biomarker for these conditions. However, further studies are needed to determine its diagnostic utility in clinical settings.
Various techniques are used to study ACOX3 protein, including Western blotting, immunohistochemistry, and mass spectrometry. In addition, genetic manipulation of cells and animal models can be used to investigate the physiological functions and regulation of ACOX3.
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