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

ALDOA Spezies: Human Wirt: Escherichia coli (E. coli) Recombinant 95 % SDS, WB, ELISA
Produktnummer ABIN7479578
  • Target Alle ALDOA Proteine anzeigen
    ALDOA (Aldolase A, Fructose-Bisphosphate (ALDOA))
    Protein-Typ
    Recombinant
    Proteineigenschaft
    AA 2-364, full length
    Spezies
    • 13
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    Human
    Quelle
    • 7
    • 5
    • 4
    • 2
    • 2
    Escherichia coli (E. coli)
    Aufreinigungstag / Konjugat
    Dieses ALDOA Protein ist gelabelt mit GST tag.
    Applikation
    SDS-PAGE (SDS), Western Blotting (WB), ELISA
    Sequenz
    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
    Reinheit
    95 %
    Top Product
    Discover our top product ALDOA Protein
  • Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Lyophilized
    Buffer
    6M guanidine hydrochloride, 20mM Tris
    Lagerung
    4 °C
  • Target
    ALDOA (Aldolase A, Fructose-Bisphosphate (ALDOA))
    Andere Bezeichnung
    Fructose-Bisphosphate Aldolase A Protein (ALDOA Produkte)
    Synonyme
    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
    Hintergrund
    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.
    Molekulargewicht
    66.7 kD
    NCBI Accession
    NM_000034
    UniProt
    P04075
    Pathways
    Ribonucleoside Biosynthetic Process
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