HSD17B4 anticorps
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- Antigène Voir toutes HSD17B4 Anticorps
- HSD17B4 (Hydroxysteroid (17-Beta) Dehydrogenase 4 (HSD17B4))
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Reactivité
- Humain, Souris, Rat
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp HSD17B4 est non-conjugé
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Application
- Western Blotting (WB), Immunohistochemistry (IHC), ELISA
- Attributs du produit
- Polyclonal Antibody
- Purification
- Affinity purification
- Immunogène
- Recombinant protein of human HSD17B4
- Isotype
- IgG
- Top Product
- Discover our top product HSD17B4 Anticorps primaire
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- Indications d'application
- WB 1:500-1:2000, IHC 1:50-1:200
- Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 0.3 mg/mL
- Buffer
- PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
- Agent conservateur
- Sodium azide
- Précaution d'utilisation
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Stock
- -20 °C
- Stockage commentaire
- Store at -20°C. Avoid freeze / thaw cycles.
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- Antigène
- HSD17B4 (Hydroxysteroid (17-Beta) Dehydrogenase 4 (HSD17B4))
- Autre désignation
- HSD17B4 (HSD17B4 Produits)
- Synonymes
- anticorps zgc:55545, anticorps zgc:77300, anticorps CG3415, anticorps DmMFE-2, anticorps Dmel\\CG3415, anticorps MFE-2, anticorps DBP, anticorps MPF-2, anticorps PRLTS1, anticorps SDR8C1, anticorps 17-beta-HSD, anticorps 17[b]-HSD, anticorps 4, anticorps MFP2, anticorps Mfp-2, anticorps perMFE-2, anticorps hydroxysteroid (17-beta) dehydrogenase 4, anticorps hydroxysteroid 17-beta dehydrogenase 4, anticorps peroxisomal Multifunctional enzyme type 2, anticorps hsd17b4, anticorps HSD17B4, anticorps Mfe2, anticorps Hsd17b4
- Sujet
- The protein encoded by this gene is a bifunctional enzyme that is involved in the peroxisomal beta-oxidation pathway for fatty acids. It also acts as a catalyst for the formation of 3-ketoacyl-CoA intermediates from both straight-chain and 2-methyl-branched-chain fatty acids. Defects in this gene that affect the peroxisomal fatty acid beta-oxidation activity are a cause of D-bifunctional protein deficiency (DBPD). An apparent pseudogene of this gene is present on chromosome 8.
- Poids moléculaire
- 80 kDa
- UniProt
- P51659
- Pathways
- Monocarboxylic Acid Catabolic Process
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