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Full length protein
Amino Acid Sequence
KANRQREPGLGFSFEFTEQQKEFQATARKFAREEIIPVAAEYDKTGEYPV PLIRRAWELGLMNTHIPENCGGLGLGTFDACLISEELAYGCTGVQTAIEG NSLGQMPIIIAGNDQQKKKYLGRMTEEPLMCAYCVTEPGAGSDVAGIKTK AEKKGDEYIINGQKMWITNGGKANWYFLLARSDPDPKAPANKAFTGFIVE ADTPGIQIGRKELNMGQRCSDTRGIVFEDVKVPKENVLIGDGAGFKVAMG AFDKTRPVVAAGAVGLAQRALDEATKYALERKTFGKLLVEHQAISFMLAE MAMKVELARMSYQRAAWEVDSGRRNTYYASIAKAFAGDIANQLATDAVQI LGGNGFNTEYPVEKLMRDAKIYQIYEGTSQIQRLIVAREHIDKYKN
46 kDa including tags
26 to 421
His tag N-Terminus
Additional sequence information
Sequence for the tag: MGSSHHHHHHSSGLVPRGSHM
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in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
Stability and Storage
Shipped on Dry Ice. Store at -20°C or -80°C. Avoid freeze / thaw cycle.
Constituents: 0.24% Tris, 0.58% Sodium chloride, 20% Glycerol ab173059 is supplied as a 0.2 µM filtered solution.
This enzyme is specific for acyl chain lengths of 4 to 16.
Lipid metabolism; mitochondrial fatty acid beta-oxidation.
Involvement in disease
Defects in ACADM are the cause of acyl-CoA dehydrogenase medium-chain deficiency (ACADMD) [MIM:201450]. It is an autosomal recessive disease which causes fasting hypoglycemia, hepatic dysfunction, and encephalopathy, often resulting in death in infancy.
Belongs to the acyl-CoA dehydrogenase family.
Information by UniProt
has not yet been referenced specifically in any publications.
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