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Aminomethyltransferase anticorps (N-Term)

AMT Reactivité: Humain, Souris, Rat, Chien, Lapin, Boeuf (Vache), Cobaye, Cheval, Poisson zèbre (Danio rerio) WB Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN406388
  • 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, Lapin, Boeuf (Vache), Cobaye, Cheval, Poisson zèbre (Danio rerio)
    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)
    Séquence
    QRAVSVVARL GFRLQAFPPA LCRPLSCAQE VLRRTPLYDF HLAHGGKMVA
    Homologie
    Cow: 100%, Dog: 100%, Guinea Pig: 100%, Horse: 100%, Human: 100%, Mouse: 100%, Rabbit: 100%, Rat: 100%, Zebrafish: 92%
    Attributs du produit
    This is a rabbit polyclonal antibody against AMT. It was validated on Western Blot using a cell lysate as a positive control.
    Purification
    Affinity Purified
    Immunogène
    The immunogen is a synthetic peptide directed towards the N terminal region of human AMT
    Top Product
    Discover our top product AMT Anticorps primaire
  • Indications d'application
    Optimal working dilutions should be determined experimentally by the investigator.
    Commentaires

    Antigen size: 403 AA

    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    Lot specific
    Buffer
    Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
    Agent conservateur
    Sodium azide
    Précaution d'utilisation
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Conseil sur la manipulation
    Avoid repeated freeze-thaw cycles.
    Stock
    -20 °C
    Stockage commentaire
    For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
  • 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.[supplied by OMIM]. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications. PRIMARYREFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-2102 D13811.1 1-2102 2103-2117 BC044792.1 3271-3285
    Alias Symbols: GCE, GCST, NKH, GCVT
    Protein Interaction Partner: HSPA8,
    Protein Size: 403
    Poids moléculaire
    44 kDa
    ID gène
    275
    NCBI Accession
    NM_000481, NP_000472
    UniProt
    P48728
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