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Aminomethyltransferase Antikörper (N-Term)

AMT Reaktivität: Human, Maus, Ratte, Hund WB Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN631086
  • Target Alle Aminomethyltransferase (AMT) Antikörper anzeigen
    Aminomethyltransferase (AMT)
    Bindungsspezifität
    • 6
    • 5
    • 4
    • 2
    • 2
    • 1
    N-Term
    Reaktivität
    • 24
    • 7
    • 6
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    Human, Maus, Ratte, Hund
    Wirt
    • 20
    • 4
    Kaninchen
    Klonalität
    • 22
    • 2
    Polyklonal
    Konjugat
    • 20
    • 2
    • 1
    • 1
    Dieser Aminomethyltransferase Antikörper ist unkonjugiert
    Applikation
    • 19
    • 8
    • 6
    • 3
    • 2
    • 2
    • 1
    • 1
    Western Blotting (WB)
    Spezifität
    AMT antibody was raised against the N terminal of AMT
    Aufreinigung
    Affinity purified
    Immunogen
    AMT antibody was raised using the N terminal of AMT corresponding to a region with amino acids QRAVSVVARLGFRLQAFPPALCRPLSCAQEVLRRTPLYDFHLAHGGKMVA
    Top Product
    Discover our top product AMT Primärantikörper
  • Applikationshinweise
    WB: 1 µg/mL
    Optimal conditions should be determined by the investigator.
    Kommentare

    AMT Blocking Peptide, catalog no. 33R-7703, is also available for use as a blocking control in assays to test for specificity of this AMT antibody

    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Lyophilized
    Rekonstitution
    Lyophilized powder. Add distilled water for a 1 mg/mL concentration of AMT antibody in PBS
    Konzentration
    Lot specific
    Buffer
    PBS
    Handhabung
    Avoid repeated freeze/thaw cycles.
    Dilute only prior to immediate use.
    Lagerung
    4 °C/-20 °C
    Informationen zur Lagerung
    Store at 2-8 °C for short periods. For longer periods of storage, store at -20 °C.
  • Target
    Aminomethyltransferase (AMT)
    Andere Bezeichnung
    AMT (AMT Produkte)
    Synonyme
    F16J13.200 antikoerper, F16J13_200 antikoerper, T7P1.13 antikoerper, T7P1_13 antikoerper, wu:fc31f04 antikoerper, wu:fd44b12 antikoerper, wu:fd54h12 antikoerper, zgc:103483 antikoerper, zgc:109741 antikoerper, GCE antikoerper, GCST antikoerper, GCVT antikoerper, NKH antikoerper, EG434437 antikoerper, aminomethyltransferase antikoerper, Glycine cleavage T-protein family antikoerper, Aminomethyltransferase antikoerper, aminomethyltransferase L homeolog antikoerper, AMT antikoerper, AT4G12130 antikoerper, AT1G60990 antikoerper, Tb11.01.1440 antikoerper, Palpr_0614 antikoerper, Ocepr_1643 antikoerper, Celal_2914 antikoerper, Deima_1002 antikoerper, Deipr_1956 antikoerper, Bacsa_3405 antikoerper, Celly_0288 antikoerper, Weevi_0527 antikoerper, Fluta_3952 antikoerper, Marky_0785 antikoerper, Spico_1217 antikoerper, Poras_1228 antikoerper, Halhy_3617 antikoerper, amt antikoerper, amt.L antikoerper, Amt antikoerper
    Hintergrund
    The enzyme system for cleavage of glycine (glycine cleavage system, EC 2.1.2.10), which is confined to the mitochondria, is composed of 4 protein components: P protein (a pyridoxal phosphate-dependent glycine decarboxylase), H protein (a lipoic acid-containing protein), T protein (a tetrahydrofolate-requiring enzyme), and L protein (a lipoamide dehydrogenase). Glycine encephalopathy (GCE) may be due to a defect in any one of these enzymes.
    Molekulargewicht
    44 kDa (MW of target protein)
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