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EHHADH Antibody

CAT: 0223-15-015Size: 100 µLDry Ice: NoHazardous: No
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CAT#:0223-15-015Size:100 µL
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Background
The protein encoded by this gene is a bifunctional enzyme and is one of the four enzymes of the peroxisomal beta-oxidation pathway. The N-terminal region of the encoded protein contains enoyl-CoA hydratase activity while the C-terminal region contains 3-hydroxyacyl-CoA dehydrogenase activity. Defects in this gene are a cause of peroxisomal disorders such as Zellweger syndrome. Two transcript variants encoding different isoforms have been found for this gene.
NCBI Gene ID
1962
Swiss Prot
Q08426
Host
Rabbit
Reactivity
Human, Mouse, Rat
Immunogen
Recombinant fusion protein containing a sequence corresponding to amino acids 444-723 of human EHHADH (NP_001957.2) .
Clonality
Polyclonal
Conjugation
Unconjugated
Type
Primary Antibodies
Field of Research
Cancer, Signal Transduction
Purification
Affinity purification
Positive Control
HepG2
Concentration
Batch dependent
Buffer
PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Modification
None
Shipping Conditions
Blue Ice
Storage Conditions
Store at -20˚ C. Avoid freeze / thaw cycles.
Calculated Molecular Weight
Observed: 79kDa
Fragment
IgG
Symbol
EHHADH
Positive Control 2
Mouse liver
Positive Control 3
Rat liver
Positive Control 4
Rat kidney
NCBI Official Name
Peroxisomal bifunctional enzyme
NCBI Organism
Homo sapiens
Other Product Names
Peroxisomal bifunctional enzyme, PBE, PBFE, Enoyl-CoA hydratase/3,2-trans-enoyl-CoA isomerase, 3-hydroxyacyl-CoA dehydrogenase, EHHADH, ECHD
Tested Applications
WB, IHC, IF
Physical Properties
Liquid

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MBS853544-01EHHADH Antibody

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