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Anti-HSD17B4 Antibody (aa134) LS-C190207

Ordering

Wt. Vol. Conc. Price
- 100 µl 0.5 mg/ml $455
Inquire for larger quantities

LSBio (Direct) LSBio (Direct)
206-374-1102
866-206-6909
Orders@LSBio.com
 

Most Popular HSD17B4 Antibodies

Anti-HSD17B4 Antibody (aa341-370, APC) LS-C215187
Rabbit Polyclonal (IgG) to Human HSD17B4
Human
IHC, Western blot, ELISA
APC Conjugated
Anti-HSD17B4 Antibody (aa341-370, Biotin) LS-C215188
Rabbit Polyclonal (IgG) to Human HSD17B4
Human
IHC, Western blot, ELISA
Biotin Conjugated
Anti-HSD17B4 Antibody (aa341-370, FITC) LS-C215190
Rabbit Polyclonal (IgG) to Human HSD17B4
Human
IHC, Western blot, ELISA
FITC Conjugated

100% Guaranteed 100% Guaranteed
Rabbit Polyclonal (IgG) to Human HSD17B4
Human, Mouse
Western blot
Unconjugated

Details

Human HSD17B4
Rabbit
Human, Mouse (tested or 100% immunogen sequence identity)
IgG Polyclonal
Unconjugated
Affinity purified
Unmodified

Applications

Western blot (1 - 4 µg/ml)

Specificity and Use

HSD17B4 antibody was raised against synthetic peptide corresponding to aa134 from human HSD17B4.
aa134
Human HSD17B4. Species Crossreactivity: mouse.

Packaging

PBS, pH 7.2, 0.5% BSA, 5 mM EDTA, 0.01% Thimerosal, 30% glycerol
May be stored at 4°C for short-term only. Aliquot to avoid repeated freezing and thawing. Store at -20°C. Aliquots are stable for 12 months.
For research use only.

About HSD17B4

P51659 NM_000414 NP_000405.1

HSD17B4 Antibody, 17-beta-HSD IV Antibody, 17-beta-HSD 4 Antibody, Beta-keto-reductase Antibody, D-bifunctional protein Antibody, EDH17B4 Antibody, MPF-2 Antibody, PRLTS1 Antibody, SDR8C1 Antibody, Beta-hydroxyacyl dehydrogenase Antibody, MFE-2 Antibody, Multifunctional protein 2 Antibody

HSD17B4 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.

Requested From: United States
Date Requested: 12/5/2016

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