EHHADH Protein (Myc-DYKDDDDK Tag)
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- Antigène Voir toutes EHHADH Protéines
- EHHADH (Enoyl-CoA, Hydratase/3-Hydroxyacyl CoA Dehydrogenase (EHHADH))
- Type de proteíne
- Recombinant
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Origine
- Humain
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Source
- HEK-293 Cells
- Purification/Conjugué
- Cette EHHADH protéine est marqué à la Myc-DYKDDDDK Tag.
- Application
- Antibody Production (AbP), Standard (STD)
- Attributs du produit
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- Recombinant human EHHADH / PBE protein expressed in HEK293 cells.
- Produced with end-sequenced ORF clone
- Pureté
- > 80 % as determined by SDS-PAGE and Coomassie blue staining
- Top Product
- Discover our top product EHHADH Protéine
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- Indications d'application
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Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays - Commentaires
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The tag is located at the C-terminal.
- Restrictions
- For Research Use only
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- Concentration
- 50 μg/mL
- Buffer
- 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
- Stock
- -80 °C
- Stockage commentaire
- Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
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- Antigène
- EHHADH (Enoyl-CoA, Hydratase/3-Hydroxyacyl CoA Dehydrogenase (EHHADH))
- Autre désignation
- Ehhadh,pbe (EHHADH Produits)
- Synonymes
- ECHD Protein, L-PBE Protein, LBFP Protein, LBP Protein, PBFE Protein, 1 Protein, Lbp Protein, MEF Protein, Mfe Protein, Mfe1 Protein, Pbe Protein, Pbfe Protein, perMFE-1 Protein, 1300002P22Rik Protein, HD Protein, MFP Protein, MFP1 Protein, zgc:77526 Protein, Ehhadh Protein, enoyl-CoA hydratase and 3-hydroxyacyl CoA dehydrogenase Protein, enoyl-CoA, hydratase/3-hydroxyacyl CoA dehydrogenase Protein, enoyl-Coenzyme A, hydratase/3-hydroxyacyl Coenzyme A dehydrogenase Protein, peroxisomal bifunctional enzyme-like Protein, EHHADH Protein, ehhadh Protein, Ehhadh Protein, LOC100135519 Protein
- Sujet
- The protein encoded by this gene is a bifunctional enzyme and is one of the four enzymes of the peroxisomal beta-oxidation pathway. The N-terminal region of the encoded protein contains enoyl-CoA hydratase activity while the C-terminal region contains 3-hydroxyacyl-CoA dehydrogenase activity. Defects in this gene are a cause of peroxisomal disorders such as Zellweger syndrome. Two transcript variants encoding different isoforms have been found for this gene.
- Poids moléculaire
- 79.3 kDa
- NCBI Accession
- NP_001957
- Pathways
- Monocarboxylic Acid Catabolic Process
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