Overview
Product nameACADM proteinSee all ACADM proteins and peptides ...
Protein descriptionRecombinant Human full length ACADM (amino acids 26-421) with a N terminal His tag; a single, non-glycosylated polypeptide chain; 417 amino acids with tag; predicted Mwt: 45.9 kDa (UniProt P11310).
Uniprot accessionP11310
Molecular weight45.900kDa
Protein length396 amino acids
Expression hostE. coli
Properties
Purity> 90
% by SDS-PAGE
E.C. Number1.3.99.3
FormLiquid
Storage instructionsPlease see Notes section
Storage bufferpH: 7.50
Constituents: 20% Glycerol, 0.32% Tris HCl
Concentration information loading...
Additional notesalthough stable at 4°C for 1 week, should be stored desiccated below -18°C. Please prevent freeze thaw cycles.
Sequence notesMGSSHHHHHH SSGLVPRGSH MKANRQREPG LGFSFEFTEQ QKEFQATARK FAREEIIPVA AEYDKTGEYP VPLIRRAWEL GLMNTHIPEN CGGLGLGTFD ACLISEELAY GCTGVQTAIE GNSLGQMPII IAGNDQQKKK YLGRMTEEPL MCAYCVTEPG AGSDVAGIKT KAEKKGDEYI INGQKMWITN GGKANWYFLL ARSDPDPKAP ANKAFTGFIV EADTPGIQIG RKELNMGQRC SDTRGIVFED VKVPKENVLI GDGAGFKVAM GAFDKTRPVV AAGAVGLAQR ALDEATKYAL ERKTFGKLLV EHQAISFMLA EMAMKVELAR MSYQRAAWEV DSGRRNTYYA SIAKAFAGDI ANQLATDAVQ ILGGNGFNTE YPVEKLMRDA KIYQIYEGTS QIQRLIVARE HIDKYKN
Research Areas
Applications
Our Abpromise guarantee covers the use of
ab117199
in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
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Application
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Notes |
| SDS-PAGE |
SDS-PAGE: Use at an assay dependent concentration. |
Application notesThis peptide can be used with studies using ab13677 and ab115277.
Protein info
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Alternative names
ACADM_HUMANAcyl coenzyme A dehydrogenaseAcyl coenzyme A dehydrogenase C 4 to C 12 straight chainFLJ18227FLJ93013FLJ99884MCADMCADHMedium chain acyl CoA dehydrogenaseMedium chain fatty acyl CoA dehydrogenaseMedium chain specific acyl CoA dehydrogenaseMedium chain specific acyl CoA dehydrogenase mitochondrialMedium-chain specific acyl-CoA dehydrogenasemitochondrial
see all
FunctionThis enzyme is specific for acyl chain lengths of 4 to 16.
PathwayLipid metabolism; mitochondrial fatty acid beta-oxidation.
Involvement in diseaseDefects 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.
Sequence similaritiesBelongs to the acyl-CoA dehydrogenase family.
Cellular localizationMitochondrion matrix.
References for ACADM protein (ab117199)
ab117199
has not yet been referenced specifically in any publications.
Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"