HSD17B4 Polyclonal Antibody
Size: 200μL
Storage: Store at -20℃ Valid for 12 months. Avoid freeze / thaw cycles.
Shipping: The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended.
Exp date: 12 months
Category ID_II: Primary Antibodies
Category ID_III: Polyclonal Antibodies
Abbreviation: HSD17B4
Target Synonym: 12-alpha-trihydroxy-5-beta-cholest-24-enoyl-CoA hydratase;17 beta HSD 4;17 beta HSD IV;17 beta hydroxysteroid dehydrogenase 4;17-beta-HSD 4;17-beta-hydroxysteroid dehydrogenase 4;17beta estradiol dehydrogenase type IV;3 alpha 7 alpha12 alpha trihydroxy 5 beta cholest 24 enoyl CoA hydratase;3-alpha;7-alpha;Beta hydroxyacyl dehydrogenase;Beta keto reductase;D 3 hydroxyacyl CoA dehydratase;D bifunctional protein;D bifunctional protein peroxisomal;D-3-hydroxyacyl CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein;D-bifunctional protein;D-bifunctional protein;peroxisomal;DBP;DBP;peroxisomal;DHB4;EDH17B4;Enoyl-CoA hydratase 2;Hsd17b4;MFE 2;MFE-2;MPF-2;Multifunctional protein 2;Peroxisomal multifunctional enzyme type 2;Peroxisomal multifunctional protein 2;PRLTS1;SDR8C1;Short chain dehydrogenase/reductase family 8C member 1
Research Areas: Cancer;Cardiovascular;Metabolism;Signal Transduction
Conjugation: Unconjugated
Host: Rabbit
Species reactivity: Human;Mouse;Rat
Application: WB;IHC
Isotype: IgG
Clonality: Polyclonal
Clone NO.:
UNIProt ID: P51659
Accession:
Background: 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.
Concentration: 0.3 mg/mL
Immunogen: Recombinant protein of human HSD17B4
Buffer: PBS with 0.05% sodium azide and 50% glycerol, PH7.4
Purification method: Affinity purification
Dilution: WB 1:500-1:2000;IHC 1:50-1:200
Calculated MW: 80kDa
ObservedMW:
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HSD17B4 Polyclonal Antibody
HSD17B4 Polyclonal Antibody
Size: 200μL
Storage: Store at -20℃ Valid for 12 months. Avoid freeze / thaw cycles.
Shipping: The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended.
Exp date: 12 months
Category ID_II: Primary Antibodies
Category ID_III: Polyclonal Antibodies
Abbreviation: HSD17B4
Target Synonym: 12-alpha-trihydroxy-5-beta-cholest-24-enoyl-CoA hydratase;17 beta HSD 4;17 beta HSD IV;17 beta hydroxysteroid dehydrogenase 4;17-beta-HSD 4;17-beta-hydroxysteroid dehydrogenase 4;17beta estradiol dehydrogenase type IV;3 alpha 7 alpha12 alpha trihydroxy 5 beta cholest 24 enoyl CoA hydratase;3-alpha;7-alpha;Beta hydroxyacyl dehydrogenase;Beta keto reductase;D 3 hydroxyacyl CoA dehydratase;D bifunctional protein;D bifunctional protein peroxisomal;D-3-hydroxyacyl CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein;D-bifunctional protein;D-bifunctional protein;peroxisomal;DBP;DBP;peroxisomal;DHB4;EDH17B4;Enoyl-CoA hydratase 2;Hsd17b4;MFE 2;MFE-2;MPF-2;Multifunctional protein 2;Peroxisomal multifunctional enzyme type 2;Peroxisomal multifunctional protein 2;PRLTS1;SDR8C1;Short chain dehydrogenase/reductase family 8C member 1
Research Areas: Cancer;Cardiovascular;Metabolism;Signal Transduction
Conjugation: Unconjugated
Host: Rabbit
Species reactivity: Human;Mouse;Rat
Application: WB;IHC
Isotype: IgG
Clonality: Polyclonal
Clone NO.:
UNIProt ID: P51659
Accession:
Background: 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.
Concentration: 0.3 mg/mL
Immunogen: Recombinant protein of human HSD17B4
Buffer: PBS with 0.05% sodium azide and 50% glycerol, PH7.4
Purification method: Affinity purification
Dilution: WB 1:500-1:2000;IHC 1:50-1:200
Calculated MW: 80kDa
ObservedMW:
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Description
Size: 200μL
Storage: Store at -20℃ Valid for 12 months. Avoid freeze / thaw cycles.
Shipping: The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended.
Exp date: 12 months
Category ID_II: Primary Antibodies
Category ID_III: Polyclonal Antibodies
Abbreviation: HSD17B4
Target Synonym: 12-alpha-trihydroxy-5-beta-cholest-24-enoyl-CoA hydratase;17 beta HSD 4;17 beta HSD IV;17 beta hydroxysteroid dehydrogenase 4;17-beta-HSD 4;17-beta-hydroxysteroid dehydrogenase 4;17beta estradiol dehydrogenase type IV;3 alpha 7 alpha12 alpha trihydroxy 5 beta cholest 24 enoyl CoA hydratase;3-alpha;7-alpha;Beta hydroxyacyl dehydrogenase;Beta keto reductase;D 3 hydroxyacyl CoA dehydratase;D bifunctional protein;D bifunctional protein peroxisomal;D-3-hydroxyacyl CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein;D-bifunctional protein;D-bifunctional protein;peroxisomal;DBP;DBP;peroxisomal;DHB4;EDH17B4;Enoyl-CoA hydratase 2;Hsd17b4;MFE 2;MFE-2;MPF-2;Multifunctional protein 2;Peroxisomal multifunctional enzyme type 2;Peroxisomal multifunctional protein 2;PRLTS1;SDR8C1;Short chain dehydrogenase/reductase family 8C member 1
Research Areas: Cancer;Cardiovascular;Metabolism;Signal Transduction
Conjugation: Unconjugated
Host: Rabbit
Species reactivity: Human;Mouse;Rat
Application: WB;IHC
Isotype: IgG
Clonality: Polyclonal
Clone NO.:
UNIProt ID: P51659
Accession:
Background: 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.
Concentration: 0.3 mg/mL
Immunogen: Recombinant protein of human HSD17B4
Buffer: PBS with 0.05% sodium azide and 50% glycerol, PH7.4
Purification method: Affinity purification
Dilution: WB 1:500-1:2000;IHC 1:50-1:200
Calculated MW: 80kDa
ObservedMW:
