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Huntingtin anticorps (N-Term)

HTT Reactivité: Humain, Rat, Souris WB, IHC, ELISA Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN2464133
  • Antigène Voir toutes Huntingtin (HTT) Anticorps
    Huntingtin (HTT)
    Épitope
    • 15
    • 5
    • 4
    • 4
    • 4
    • 4
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    N-Term
    Reactivité
    • 63
    • 45
    • 36
    • 6
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Humain, Rat, Souris
    Hôte
    • 60
    • 21
    • 2
    Lapin
    Clonalité
    • 53
    • 29
    Polyclonal
    Conjugué
    • 55
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp Huntingtin est non-conjugé
    Application
    • 40
    • 32
    • 24
    • 14
    • 14
    • 13
    • 13
    • 9
    • 7
    • 4
    • 4
    • 2
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC), ELISA
    Purification
    Affinity Purified
    Immunogène
    A synthetic peptide corresponding to the N-terminus.
    Isotype
    IgG
    Top Product
    Discover our top product HTT Anticorps primaire
  • Indications d'application
    ELISA, Western (immuno) blotting, Immunostaining (in testing)
    Restrictions
    For Research Use only
  • Antigène
    Huntingtin (HTT)
    Autre désignation
    Huntington Protein (HTT Produits)
    Synonymes
    anticorps HTT, anticorps hd, anticorps ZHD, anticorps CG9995, anticorps Dmel\\CG9995, anticorps HD, anticorps Hsap\\HD, anticorps Htt, anticorps dHtt, anticorps dhtt, anticorps SLC6A4, anticorps huntington, anticorps it15, anticorps htt, anticorps IT15, anticorps AI256365, anticorps C430023I11Rik, anticorps Hd, anticorps Hdh, anticorps huntingtin, anticorps HTT, anticorps htt, anticorps LOC373520, anticorps Htt
    Sujet
    Huntington's disease (HD) is an autosomal dominant neurological disorder caused by a polyglutamine (polyQ) repeat expansion in the huntingtin (Htt) protein. The disease is characterized by neurodegeneration and formation of neuronal intracellular inclusions primarily in the striatum and cortex, leading to personality changes, motor impairment, and dementia. The Huntington s disease protein is ~350 kDa in size and is localized in the brain.
    ID gène
    3064
    UniProt
    P42858
    Pathways
    Signalisation PI3K-Akt, Hormone Transport, Transition Metal Ion Homeostasis, Tube Formation, Protein targeting to Nucleus, Dicarboxylic Acid Transport
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