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17β-HSD4 Rabbit pAb

-YT5386

Catalog: YT5386
Size
Price
Status
Qty.
200μL
$450.00
In stock

0

100μL
$280.00
In stock

0

40μL
$150.00
In stock

0

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Main Information
Target

17β-HSD4

Host Species

Rabbit

Reactivity

Human, Mouse, Rat

Applications

WB, IHC, IF, ELISA

MW

80kD (Observed)

Conjugate/Modification


Unmodified

Detailed Information
Recommended Dilution Ratio
WB 1:500-1:2000; IHC: 1:100-1:300; ELISA 1:20000; IF 1:50-200
Formulation
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Specificity
17β-HSD4 Polyclonal Antibody detects endogenous levels of 17β-HSD4 protein.
Purification
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Storage
-15°C to -25°C/1 year(Do not lower than -25°C)
Concentration
1 mg/ml
MW(Observed)
80kD
Modification
Unmodified
Clonality
Polyclonal
Isotype
IgG
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Antigen&Target Information
Immunogen:
The antiserum was produced against synthesized peptide derived from the N-terminal region of human HSD17B4. AA range:41-90
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Specificity:
17β-HSD4 Polyclonal Antibody detects endogenous levels of 17β-HSD4 protein.
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Gene Name:
HSD17B4
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Protein Name:
Peroxisomal multifunctional enzyme type 2
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Other Name:
HSD17B4 ;
EDH17B4 ;
Peroxisomal multifunctional enzyme type 2 ;
MFE-2 ;
17-beta-hydroxysteroid dehydrogenase 4 ;
17-beta-HSD 4 ;
D-bifunctional protein ;
DBP ;
Multifunctional protein 2 ;
MPF-2
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Database Link:
Organism Gene ID SwissProt
Human 3295; P51659;
Mouse 15488; P51660;
Rat 79244; P97852;
Background:
hydroxysteroid 17-beta dehydrogenase 4(HSD17B4) Homo sapiens 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. Multiple alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, May 2014],
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Function:
Catalytic activity:(24R,25R)-3-alpha,7-alpha,12-alpha,24-tetrahydroxy-5-beta-cholestanoyl-CoA = (24E)-3-alpha,7-alpha,12-alpha-trihydroxy-5-beta-cholest-24-enoyl-CoA + H(2)O.,Catalytic activity:(S)-3-hydroxyacyl-CoA + NAD(+) = 3-oxoacyl-CoA + NADH.,Disease:Defects in HSD17B4 are a cause of D-bifunctional protein deficiency (DBPD) [MIM:261515]. DBPD is a disorder of peroxisomal fatty acid beta-oxidation.,Function:Bifunctional enzyme acting on the peroxisomal beta-oxidation pathway for fatty acids. Catalyzes the formation of 3-ketoacyl-CoA intermediates from both straight-chain and 2-methyl-branched-chain fatty acids.,pathway:Lipid metabolism; fatty acid beta-oxidation.,similarity:Belongs to the short-chain dehydrogenases/reductases (SDR) family.,similarity:Contains 1 SCP2 domain.,tissue specificity:Present in many tissues with highest concentrations in liver, heart, prostate and testis.,
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Cellular Localization:
Peroxisome .
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Tissue Expression:
Present in many tissues with highest concentrations in liver, heart, prostate and testis.
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Research Areas:
>>Primary bile acid biosynthesis ;
>>Biosynthesis of unsaturated fatty acids ;
>>Metabolic pathways ;
>>Fatty acid metabolism ;
>>Peroxisome
show all
Catalog: YT5386
Size
Price
Status
Qty.
200μL
$450.00
In stock

0

100μL
$280.00
In stock

0

40μL
$150.00
In stock

0

Add to cart

Collected

Collect

Customized Service

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