Recombinant人ACADS protein (ab95383)

概述

  • 产品名称
    Recombinant人ACADS protein
  • 蛋白长度
    Full length protein

描述

  • 性质
    Recombinant
  • 来源
    Escherichia coli
  • 氨基酸序列
    • 种属
      Human
    • 序列
      MGSSHHHHHH 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

技术指标

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.

  • 应用

    Mass Spectrometry

    SDS-PAGE

  • 纯度
    > 95 % SDS-PAGE.
    ab95383 is purified using conventional chromatography techniques.
  • 形式
    Liquid
  • Concentration information loading...

制备和贮存

  • 稳定性和存储

    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

常规信息

  • 别名
    • 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
  • 通路
    Lipid metabolism; mitochondrial fatty acid beta-oxidation.
  • 疾病相关
    Defects 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.
  • 序列相似性
    Belongs to the acyl-CoA dehydrogenase family.
  • 细胞定位
    Mitochondrion matrix.
  • Information by UniProt

图片

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

文献

ab95383 has not yet been referenced specifically in any publications.

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Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"

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