Overview

Description

  • NatureRecombinant
  • SourceE. coli
  • Amino Acid Sequence
    • SpeciesHuman
    • SequenceMGSSHHHHHH SSGLVPRGSH MLHTIYQSVE LPETHQMLLQ TCRDFAEKEL FPIAAQVDKE HLFPAAQVKK MGGLGLLAMD VPEELGGAGL DYLAYAIAME EISRGCASTG VIMSVNNSLY LGPILKFGSK EQKQAWVTPF TSGDKIGCFA LSEPGNGSDA GAASTTARAE GDSWVLNGTK AWITNAWEAS AAVVFASTDR ALQNKSISAF LVPMPTPGLT LGKKEDKLGI RGSSTANLIF EDCRIPKDSI LGEPGMGFKI AMQTLDMGRI GIASQALGIA QTALDCAVNY AENRMAFGAP LTKLQVIQFK LADMALALES ARLLTWRAAM LKDNKKPFIK EAAMAKLAAS EAATAISHQA IQILGGMGYV TEMPAERHYR DARITEIYEG TSEIQRLVIA GHLLRSYRS
    • Amino acids0 to 0

Specifications

Our Abpromise guarantee covers the use of ab95383 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

  • Applications

    Mass Spectrometry

    SDS-PAGE

  • Purity> 95 % by SDS-PAGE.
    ab95383 is purified using conventional chromatography techniques.
  • FormLiquid
  • Concentration information loading...

Preparation and Storage

  • Stability and Storage

    Shipped at 4°C. Upon delivery aliquot and store at -20°C or -80°C. Avoid repeated freeze / thaw cycles.

    Preservative: None
    Constituents: 20% Glycerol, 0.1M Sodium chloride, 20mM Tris HCl, 1mM DTT, pH 8.0

General info

  • Alternative names
    • ACAD3
    • ACADS
    • ACADS_HUMAN
    • Acyl Coenzyme A dehydrogenase, C2 to C3 short chain
    • Acyl-CoA dehydrogenase, C2 to C3 short chain
    • Acyl-CoA dehydrogenase, short chain
    • Acyl-Coenzyme A dehydrogenase, short chain
    • AI196007
    • Bcd-1
    • Bcd1
    • Butyryl CoA dehydrogenase
    • Butyryl-CoA dehydrogenase
    • EC 1.3.99.2
    • mitochondrial
    • SCAD
    • Short chain acyl CoA dehydrogenase
    • Short-chain specific acyl-CoA dehydrogenase
    • Short-chain specific acyl-CoA dehydrogenase, mitochondrial
    • Unsaturated acyl CoA reductase
    see all
  • PathwayLipid metabolism; mitochondrial fatty acid beta-oxidation.
  • Involvement in diseaseDefects in ACADS are the cause of acyl-CoA dehydrogenase short-chain deficiency (ACADSD) [MIM:201470]. It is an autosomal recessive disorder resulting in acute acidosis and muscle weakness in infants, and a form of lipid-storage myopathy in adults.
  • Sequence similaritiesBelongs to the acyl-CoA dehydrogenase family.
  • Cellular localizationMitochondrion matrix.
  • Target information above from: UniProt accession P16219 The UniProt Consortium
    The Universal Protein Resource (UniProt) in 2010
    Nucleic Acids Res. 38:D142-D148 (2010) .

    Information by UniProt

Human ACADS full length protein images

  • 15% SDS-PAGE analysis of 3µg ab95383.

References for Human ACADS full length protein (ab95383)

ab95383 has not yet been referenced specifically in any publications.

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