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Aminomethyltransferase anticorps

AMT Reactivité: Humain, Souris, Rat, Chien WB, ELISA Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN2459732
  • Antigène Voir toutes Aminomethyltransferase (AMT) Anticorps
    Aminomethyltransferase (AMT)
    Reactivité
    • 23
    • 6
    • 5
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    Humain, Souris, Rat, Chien
    Hôte
    • 19
    • 4
    Lapin
    Clonalité
    • 21
    • 2
    Polyclonal
    Conjugué
    • 19
    • 2
    • 1
    • 1
    Cet anticorp Aminomethyltransferase est non-conjugé
    Application
    • 18
    • 7
    • 6
    • 3
    • 2
    • 2
    • 1
    • 1
    Western Blotting (WB), ELISA
    Purification
    Antibody is purified by peptide affinity chromatography method.
    Immunogène
    Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human AMT.
    Top Product
    Discover our top product AMT Anticorps primaire
  • Indications d'application
    AMT antibody can be used for detection of AMT by ELISA at 1:12500. AMT antibody can be used for detection of AMT by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.
    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Reconstitution
    Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.
    Concentration
    1 mg/mL
    Buffer
    Antibody is lyophilized in PBS buffer with 2 % sucrose.
    Conseil sur la manipulation
    As with any antibody avoid repeat freeze-thaw cycles.
    Stock
    4 °C/-20 °C
    Stockage commentaire
    For short periods of storage (days) store at 4 °C. For longer periods of storage, store AMT antibody 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.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, MIM 238300), H protein (a lipoic acid-containing protein, MIM 238330), T protein (a tetrahydrofolate-requiring enzyme), and L protein (a lipoamide dehydrogenase, MIM 238331). Glycine encephalopathy (GCE, MIM 605899) may be due to a defect in any one of these enzymes.
    Poids moléculaire
    44 kDa
    ID gène
    275
    NCBI Accession
    NP_000472
    UniProt
    P48728
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