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>   home   >   Products   >   Primary Antibodies   >   Signal Transduction   >   EHHADH Antibody   

EHHADH Antibody

Rabbit Polyclonal Antibody

  • WB - EHHADH Antibody ABV11229
    Western blot with EHHADH antibody. Lane 1: 45 μg of Jurkat cell lysate; Lane 2: 45 μg of 3T3 cell lysate
Product Information
  • Applications Legend:
  • WB=Western Blot
  • IHC=Immunohistochemistry
  • IHC-P=Immunohistochemistry (Paraffin-embedded Sections)
  • IHC-F=Immunohistochemistry (Frozen Sections)
  • IF=Immunofluorescence
  • FC=Flow Cytopmetry
  • IC=Immunochemistry
  • ICC=Immunocytochemistry
  • IP=Immunoprecipitation
  • DB=Dot Blot
  • CHIP=Chromatin Immunoprecipitation
  • FA=Fluorescence Assay
  • IEM=Immunoelectronmicroscopy
  • EIA=Enzyme Immunoassay
Primary Accession Q08426
Reactivity Human
Host Rabbit
Clonality Polyclonal
Isotype Rabbit IgG
Calculated MW 79495 Da
Additional Information
Gene ID 1962
Positive Control Western Blot: Jurkat cell lysate, 3T3 cell lysate
Application & Usage Western blot: 1-4 µg
Other Names Enoyl-CoA, hydratase/3-hydroxyacyl CoA dehydrogenase, LBFP, LBP, L-PBE, peroxisomal bifunctional enzyme3, 2-trans-enoyl-CoA isomerase, peroxisomal enoyl-CoA hydratase
Target/Specificity EHHADH
Antibody Form Liquid
Appearance Colorless liquid
Formulation 100 µg (0.5 mg/ml) of Caspase-10 antibody in PBS pH 7.2, 0.01 % BSA, 0.01 % thimerosal, and 50 % glycerol.
Handling The antibody solution should be gently mixed before use.
Reconstitution & Storage -20 °C
Background Descriptions
PrecautionsEHHADH Antibody is for research use only and not for use in diagnostic or therapeutic procedures.
Protein Information
Synonyms ECHD
Cellular Location Peroxisome.
Tissue Location Liver and kidney. Strongly expressed in the terminal segments of the proximal tubule. Lower amounts seen in the brain.
Research Areas
Citations (0)

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EHHADH is a bifunctional enzyme. It is one of the four enzymes of the peroxisomal beta-oxidation pathway. The N-terminal region of this 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. EHHADH-null mice only exhibit a blunted peroxisome proliferative response when challenged with a peroxisome proliferator.

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$ 265.00
$ 89.00
Cat# ABV11229
(40 western blots)
Availability: 5-7days
Bulk Size
Seasonal Special on Bulk Order
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