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HSD17B4 antibody
HSD17B4
Reactivity: Human, Mouse, Rat
WB, IHC, ELISA
Host: Rabbit
Polyclonal
unconjugated
Product Details anti-HSD17B4 Antibody
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Target
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HSD17B4
(Hydroxysteroid (17-Beta) Dehydrogenase 4 (HSD17B4))
Reactivity
All reactivities for HSD17B4 antibodies
Human, Mouse, Rat
Host
All hosts for HSD17B4 antibodies
Rabbit
Clonality
All clonalities for HSD17B4 antibodies
Polyclonal
Conjugate
All conjugates for HSD17B4 antibodies
This HSD17B4 antibody is un-conjugated
Application
All applications for HSD17B4 antibodies
Western Blotting (WB), Immunohistochemistry (IHC), ELISA
Characteristics
Polyclonal Antibody
Purification
Affinity purification
Immunogen
Recombinant protein of human HSD17B4
Isotype
IgG
Top Product
Discover our top product HSD17B4 Primary Antibody
Alternatives
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Application Details
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Application Notes
WB 1:500-1:2000, IHC 1:50-1:200
Restrictions
For Research Use only
Handling
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Format
Liquid
Concentration
0.3 mg/mL
Buffer
PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
Preservative
Sodium azide
Precaution of Use
This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Storage
-20 °C
Storage Comment
Store at -20°C. Avoid freeze / thaw cycles.
Target Details for HSD17B4
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Target
HSD17B4
(Hydroxysteroid (17-Beta) Dehydrogenase 4 (HSD17B4))
Alternative Name
HSD17B4 (HSD17B4 Products )
Synonyms
zgc:55545 antibody, zgc:77300 antibody, CG3415 antibody, DmMFE-2 antibody, Dmel\\CG3415 antibody, MFE-2 antibody, DBP antibody, MPF-2 antibody, PRLTS1 antibody, SDR8C1 antibody, 17-beta-HSD antibody, 17[b]-HSD antibody, 4 antibody, MFP2 antibody, Mfp-2 antibody, perMFE-2 antibody, hydroxysteroid (17-beta) dehydrogenase 4 antibody, hydroxysteroid 17-beta dehydrogenase 4 antibody, peroxisomal Multifunctional enzyme type 2 antibody, hsd17b4 antibody, HSD17B4 antibody, Mfe2 antibody, Hsd17b4 antibody
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.
Molecular Weight
80 kDa
UniProt
P51659
Pathways
Monocarboxylic Acid Catabolic Process
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