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

Recombinant Human ACADS protein 图像

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

Recombinant Human ACADS protein (ab95383)参考文献

ab95383 has not yet been referenced specifically in any publications.

Product Wall

There are currently no Abreviews or Questions for ab95383.
Please use the links above to contact us or submit feedback about this product.

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