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Catalog: YT3610
Size
Price
Status
Qty.
200μL
$450.00
In stock

0

100μL
$280.00
In stock

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40μL
$150.00
In stock

0

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Main Information
Target

PBFE

Host Species

Rabbit

Reactivity

Human, 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 1:10000; IF 1:50-200
Formulation
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Specificity
PBFE Polyclonal Antibody detects endogenous levels of PBFE 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 human EHHADH. AA range:476-525
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Specificity:
PBFE Polyclonal Antibody detects endogenous levels of PBFE protein.
show all
Gene Name:
EHHADH
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Protein Name:
Peroxisomal bifunctional enzyme
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Other Name:
EHHADH ;
ECHD ;
Peroxisomal bifunctional enzyme ;
PBE ;
PBFE
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Database Link:
Organism Gene ID SwissProt
Human 1962; Q08426;
Mouse Q9DBM2;
Rat 171142; P07896;
Background:
catalytic activity:(3S)-3-hydroxyacyl-CoA = trans-2(or 3)-enoyl-CoA + H(2)O.,catalytic activity:(3Z)-dodec-3-enoyl-CoA = (2E)-dodec-2-enoyl-CoA.,catalytic activity:(S)-3-hydroxyacyl-CoA + NAD(+) = 3-oxoacyl-CoA + NADH.,disease:Absent in patients suffering with peroxisomal disorders such as Zellweger syndrome, neonatal adrenoleukodystrophy and infantile Refsum disease.,pathway:Lipid metabolism; fatty acid beta-oxidation.,similarity:In the C-terminal section; belongs to the 3-hydroxyacyl-CoA dehydrogenase family.,similarity:In the N-terminal section; belongs to the enoyl-CoA hydratase/isomerase family.,subunit:Monomer.,tissue specificity:Liver and kidney. Lower amounts seen in the brain.,
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Function:
Catalytic activity:(3S)-3-hydroxyacyl-CoA = trans-2(or 3)-enoyl-CoA + H(2)O.,Catalytic activity:(3Z)-dodec-3-enoyl-CoA = (2E)-dodec-2-enoyl-CoA.,Catalytic activity:(S)-3-hydroxyacyl-CoA + NAD(+) = 3-oxoacyl-CoA + NADH.,Disease:Absent in patients suffering with peroxisomal disorders such as Zellweger syndrome, neonatal adrenoleukodystrophy and infantile Refsum disease.,pathway:Lipid metabolism; fatty acid beta-oxidation.,similarity:In the C-terminal section; belongs to the 3-hydroxyacyl-CoA dehydrogenase family.,similarity:In the N-terminal section; belongs to the enoyl-CoA hydratase/isomerase family.,subunit:Monomer.,tissue specificity:Liver and kidney. Lower amounts seen in the brain.,
show all
Cellular Localization:
Peroxisome .
show all
Tissue Expression:
Liver and kidney. Strongly expressed in the terminal segments of the proximal tubule. Lower amounts seen in the brain.
show all
Research Areas:
>>Fatty acid degradation ;
>>Valine, leucine and isoleucine degradation ;
>>Lysine degradation ;
>>Tryptophan metabolism ;
>>beta-Alanine metabolism ;
>>Propanoate metabolism ;
>>Butanoate metabolism ;
>>Metabolic pathways ;
>>Fatty acid metabolism ;
>>PPAR signaling pathway ;
>>Peroxisome
show all
Catalog: YT3610
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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