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PEMT anticorps (C-Term)

PEMT Reactivité: Humain, Souris WB, IHC (p) Hôte: Lapin Polyclonal RB12628 unconjugated
N° du produit ABIN387868
  • Antigène Voir toutes PEMT Anticorps
    PEMT (Phosphatidylethanolamine N-Methyltransferase (PEMT))
    Épitope
    • 9
    • 8
    • 7
    • 6
    • 5
    • 3
    AA 170-199, C-Term
    Reactivité
    • 46
    • 19
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Humain, Souris
    Hôte
    • 45
    • 1
    Lapin
    Clonalité
    • 46
    Polyclonal
    Conjugué
    • 15
    • 6
    • 6
    • 5
    • 4
    • 4
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp PEMT est non-conjugé
    Application
    • 34
    • 30
    • 14
    • 2
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
    Purification
    This antibody is purified through a protein A column, followed by peptide affinity purification.
    Immunogène
    This PEMT antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 170-199 amino acids from the C-terminal region of human PEMT.
    Clone
    RB12628
    Isotype
    Ig Fraction
  • Indications d'application
    WB: 1:1000. IHC-P: 1:100. IHC-P: 1:100
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
    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.
    Stock
    4 °C,-20 °C
    Stockage commentaire
    Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.
    Date de péremption
    6 months
  • Antigène
    PEMT (Phosphatidylethanolamine N-Methyltransferase (PEMT))
    Autre désignation
    PEMT (PEMT Produits)
    Sujet
    PEMT is an enzyme which converts phosphatidylethanolamine to phosphatidylcholine by sequential methylation in the liver. The protein localizes to the endoplasmic reticulum and mitochondria-associated membranes. The gene is within the Smith-Magenis syndrome region on chromosome 17.
    Poids moléculaire
    22134
    ID gène
    10400
    NCBI Accession
    NP_001254480, NP_001254481, NP_009100, NP_680477, NP_680478
    UniProt
    Q9UBM1
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