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Aminomethyltransferase anticorps (N-Term)

AMT Reactivité: Humain, Souris, Rat, Chien WB Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN631086
  • Antigène Voir toutes Aminomethyltransferase (AMT) Anticorps
    Aminomethyltransferase (AMT)
    Épitope
    • 6
    • 5
    • 4
    • 2
    • 2
    • 1
    N-Term
    Reactivité
    • 24
    • 7
    • 6
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    Humain, Souris, Rat, Chien
    Hôte
    • 20
    • 4
    Lapin
    Clonalité
    • 22
    • 2
    Polyclonal
    Conjugué
    • 20
    • 2
    • 1
    • 1
    Cet anticorp Aminomethyltransferase est non-conjugé
    Application
    • 19
    • 8
    • 6
    • 3
    • 2
    • 2
    • 1
    • 1
    Western Blotting (WB)
    Specificité
    AMT antibody was raised against the N terminal of AMT
    Purification
    Affinity purified
    Immunogène
    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 Anticorps primaire
  • Indications d'application
    WB: 1 µg/mL
    Optimal conditions should be determined by the investigator.
    Commentaires

    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

    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Reconstitution
    Lyophilized powder. Add distilled water for a 1 mg/mL concentration of AMT antibody in PBS
    Concentration
    Lot specific
    Buffer
    PBS
    Conseil sur la manipulation
    Avoid repeated freeze/thaw cycles.
    Dilute only prior to immediate use.
    Stock
    4 °C/-20 °C
    Stockage commentaire
    Store at 2-8 °C for short periods. For longer periods of storage, store at -20 °C.
  • Antigène
    Aminomethyltransferase (AMT)
    Autre désignation
    AMT (AMT Produits)
    Synonymes
    anticorps F16J13.200, anticorps F16J13_200, anticorps T7P1.13, anticorps T7P1_13, anticorps wu:fc31f04, anticorps wu:fd44b12, anticorps wu:fd54h12, anticorps zgc:103483, anticorps zgc:109741, anticorps GCE, anticorps GCST, anticorps GCVT, anticorps NKH, anticorps EG434437, anticorps aminomethyltransferase, anticorps Glycine cleavage T-protein family, anticorps Aminomethyltransferase, anticorps aminomethyltransferase L homeolog, anticorps AMT, anticorps AT4G12130, anticorps AT1G60990, anticorps Tb11.01.1440, anticorps Palpr_0614, anticorps Ocepr_1643, anticorps Celal_2914, anticorps Deima_1002, anticorps Deipr_1956, anticorps Bacsa_3405, anticorps Celly_0288, anticorps Weevi_0527, anticorps Fluta_3952, anticorps Marky_0785, anticorps Spico_1217, anticorps Poras_1228, anticorps Halhy_3617, anticorps amt, anticorps amt.L, anticorps Amt
    Sujet
    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.
    Poids moléculaire
    44 kDa (MW of target protein)
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