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ALDOA Protein (AA 2-364, full length) (GST tag)

ALDOA Origine: Humain Hôte: Escherichia coli (E. coli) Recombinant 95 % SDS, WB, ELISA
N° du produit ABIN7479578
  • Antigène Voir toutes ALDOA Protéines
    ALDOA (Aldolase A, Fructose-Bisphosphate (ALDOA))
    Type de proteíne
    Recombinant
    Attributs du protein
    AA 2-364, full length
    Origine
    • 13
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    Humain
    Source
    • 7
    • 5
    • 4
    • 2
    • 2
    Escherichia coli (E. coli)
    Purification/Conjugué
    Cette ALDOA protéine est marqué à la GST tag.
    Application
    SDS-PAGE (SDS), Western Blotting (WB), ELISA
    Séquence
    PYQYPALTPE QKKELSDIAH RIVAPGKGIL AADESTGSIA KRLQSIGTEN TEENRRFYRQ LLLTADDRVN PCIGGVILFH ETLYQKADDG RPFPQVIKSK GGVVGIKVDK GVVPLAGTNG ETTTQGLDGL SERCAQYKKD GADFAKWRCV LKIGEHTPSA LAIMENANVL ARYASICQQN GIVPIVEPEI LPDGDHDLKR CQYVTEKVLA AVYKALSDHH IYLEGTLLKP NMVTPGHACT QKFSHEEIAM ATVTALRRTV PPAVTGITFL SGGQSEEEAS INLNAINKCP LLKPWALTFS YGRALQASAL KAWGGKKENL KAAQEEYVKR ALANSLACQG KYTPSGQAGA AASESLFVSN HAY
    Pureté
    95 %
    Top Product
    Discover our top product ALDOA Protéine
  • Restrictions
    For Research Use only
  • Format
    Lyophilized
    Buffer
    6M guanidine hydrochloride, 20mM Tris
    Stock
    4 °C
  • Antigène
    ALDOA (Aldolase A, Fructose-Bisphosphate (ALDOA))
    Autre désignation
    Fructose-Bisphosphate Aldolase A Protein (ALDOA Produits)
    Synonymes
    ALDA Protein, GSD12 Protein, aldoa Protein, cb79 Protein, sb:cb79 Protein, wu:fa28b10 Protein, wu:fb10b11 Protein, ALDOA Protein, Aldo-1 Protein, Aldo1 Protein, RNALDOG5 Protein, hm:zeh0036 Protein, zgc:77696 Protein, aldolase, fructose-bisphosphate A Protein, aldolase a, fructose-bisphosphate, a Protein, aldolase, fructose-bisphosphate A S homeolog Protein, aldolase A, fructose-bisphosphate Protein, aldolase a, fructose-bisphosphate, b Protein, ALDOA Protein, aldoaa Protein, aldoa Protein, aldoa.S Protein, Aldoa Protein, aldoab Protein
    Sujet
    Background: 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. Synonyms: Lung cancer antigen NY-LU-1 Muscle-type aldolase.
    Poids moléculaire
    66.7 kD
    NCBI Accession
    NM_000034
    UniProt
    P04075
    Pathways
    Ribonucleoside Biosynthetic Process
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