HSD17B4 polyclonal antibody
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Specification
Product Description
Rabbit polyclonal antibody raised against recombinant HSD17B4.
Immunogen
Recombinant protein corresponding to amino acids of human HSD17B4.
Sequence
LRFDGRVVLVTGAGAGLGRAYALAFAERGALVVVNDLGGDFKGVGKGSLAADKVVEEIRRRGGKAVANYDSVEEGEKVVKTALDAFG
Host
Rabbit
Reactivity
Human
Form
Liquid
Purification
Antigen affinity purification
Isotype
IgG
Recommend Usage
Immunohistochemistry (1:200-1:500)
Western Blot (1:250-1:500)
Immunofluorescence (1-4 ug/mL)
The optimal working dilution should be determined by the end user.Storage Buffer
In PBS, pH 7.2 (40% glycerol, 0.02% sodium azide)
Storage Instruction
Store at 4°C. For long term storage store at -20°C.
Aliquot to avoid repeated freezing and thawing.Note
This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Applications
Western Blot
Western blot analysis of Lane 1: RT-4, Lane 2: U-251 MG, Lane 3: Human Plasma, Lane 4: Liver, Lane 5: Tonsil with HSD17B4 polyclonal antibody (Cat # PAB21383) at 1:250-1:500 dilution.Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
Immunohistochemical staining of human liver with HSD17B4 polyclonal antibody (Cat # PAB21383) shows strong cytoplasmic positivity in hepatocytes at 1:200-1:500 dilution.Immunofluorescence
Immunofluorescent staining of human cell line A-431 with HSD17B4 polyclonal antibody (Cat # PAB21383) at 1-4 ug/mL dilution shows positivity in vesicles. -
Gene Info — HSD17B4
Entrez GeneID
3295Protein Accession#
P51659Gene Name
HSD17B4
Gene Alias
DBP, MFE-2, SDR8C1
Gene Description
hydroxysteroid (17-beta) dehydrogenase 4
Gene Ontology
HyperlinkGene Summary
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. [provided by RefSeq
Other Designations
17-beta-HSD IV|17-beta-hydroxysteroid dehydrogenase 4|17beta-estradiol dehydrogenase type IV|3-alpha,7-alpha,12-alpha-trihydroxy-5-beta-cholest-24-enoyl-CoA hydratase|D-3-hydroxyacyl-CoA dehydratase|D-bifunctional protein, peroxisomal|beta-hydroxyacyl deh
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Interactome
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Pathway
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Disease
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