Recombinant Human Aldolase protein (ab88287)

製品の概要

  • 製品名Recombinant Human Aldolase protein
  • タンパク質長Full length protein

製品の詳細

  • 由来Recombinant
  • 由来Saccharomyces cerevisiae
  • アミノ酸配列
    • 生物種Human
    • 配列MPYQYPALTPEQKKELSDIAHRIVAPGKGILAADESTGSIAKRLQSIGTE NTEENRRFY RQLLLTADDRVNPCIGGVILFHETLYQKADDGRPFPQVI KSKGGVVGIKVDKGVVPLAG TNGETTTQGLDGLSERCAQYKKDGADFA KWRCVLKIGEHTPSALAIMENANVLARYASI CQQNGIVPIVEPEILPD GDHDLKRCQYVTEKVLAAVYKALSDHHIYLEGTLLKPNMVTP GHACTQ KFSHEEIAMATVTALRRTVPPAVTGITFLSGGQSEEEASINLNAINKCPL LKP WALTFSYGRALQASALKAWGGKKENLKAAQEEYVKRALANSLACQ GKYTPSGQAGAAAS ESLFVSNHAY

特性

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.

  • アプリケーション

    SDS-PAGE

    Western blot

  • 精製度> 90 % SDS-PAGE.
    ab88287 was purified by affinity chromatography.
  • 製品の状態Liquid
  • Concentration information loading...

前処理および保存

  • 保存方法および安定性

    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

関連情報

  • 別名
    • 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
  • 機能Plays a key role in glycolysis and gluconeogenesis. In addition, may also function as scaffolding protein.
  • パスウェイCarbohydrate degradation; glycolysis; D-glyceraldehyde 3-phosphate and glycerone phosphate from D-glucose: step 4/4.
  • 関連疾患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.
  • 配列類似性Belongs to the class I fructose-bisphosphate aldolase family.
  • Information by UniProt

Recombinant Human Aldolase protein (ab88287) 使用論文

ab88287 has not yet been referenced specifically in any publications.

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