Recombinant人Aldolase protein (ab88287)

概述

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

描述

  • 性质Recombinant
  • 来源Saccharomyces cerevisiae
  • 氨基酸序列
    • 种属Human
    • 序列MPYQYPALTPEQKKELSDIAHRIVAPGKGILAADESTGSIAKRLQSIGTE NTEENRRFY RQLLLTADDRVNPCIGGVILFHETLYQKADDGRPFPQVI KSKGGVVGIKVDKGVVPLAG TNGETTTQGLDGLSERCAQYKKDGADFA KWRCVLKIGEHTPSALAIMENANVLARYASI CQQNGIVPIVEPEILPD GDHDLKRCQYVTEKVLAAVYKALSDHHIYLEGTLLKPNMVTP GHACTQ KFSHEEIAMATVTALRRTVPPAVTGITFLSGGQSEEEASINLNAINKCPL LKP WALTFSYGRALQASALKAWGGKKENLKAAQEEYVKRALANSLACQ GKYTPSGQAGAAAS ESLFVSNHAY

技术指标

Our Abpromise guarantee covers the use of ab88287 in the following tested applications.

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

  • 应用

    SDS-PAGE

    Western blot

  • 纯度> 90 % SDS-PAGE.
    ab88287 was purified by affinity chromatography.
  • 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. Avoid freeze / thaw cycles.

    Preservative: None
    Constituents: 30% Glycerol, 0.5% Triton-X-100, 50mM HEPES, 30mM Glutathione, 100mM Sodium chloride, 1mM DTT, pH 7.5

常规信息

  • 别名
    • ALDA
    • Aldo1
    • ALDOA
    • ALDOA_HUMAN
    • Aldolase 1
    • Aldolase A
    • Aldolase A fructose bisphosphatase
    • Aldolase A fructose bisphosphate
    • FRUCTOALDOLASE A
    • Fructose 1 6 bisphosphate triosephosphate lyase
    • Fructose bisphosphate aldolase
    • Fructose bisphosphate aldolase A
    • FRUCTOSE-1,6-BISPHOSPHATE ALDOLASE A
    • Fructose-bisphosphate aldolase A
    • Fructose-bisphosphate aldolase A Muscle-type
    • GSD12
    • Lung cancer antigen NY LU 1
    • Lung cancer antigen NY-LU-1
    • MGC10942
    • MGC17716
    • MGC17767
    • Muscle type aldolase
    • Muscle-type aldolase
    • RNALDOG5
    see all
  • 功能Plays a key role in glycolysis and gluconeogenesis. In addition, may also function as scaffolding protein.
  • 通路Carbohydrate degradation; glycolysis; D-glyceraldehyde 3-phosphate and glycerone phosphate from D-glucose: step 4/4.
  • 疾病相关Defects in ALDOA are the cause of glycogen storage disease type 12 (GSD12) [MIM:611881]; also known as red cell aldolase deficiency. A metabolic disorder associated with increased hepatic glycogen and hemolytic anemia. It may lead to myopathy with exercise intolerance and rhabdomyolysis.
  • 序列相似性Belongs to the class I fructose-bisphosphate aldolase family.
  • Information by UniProt

Recombinant Human Aldolase protein (ab88287)参考文献

ab88287 has not yet been referenced specifically in any publications.

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