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Huntingtin antibody (N-Term)

HTT Reactivity: Human, Rat, Mouse WB, IHC, ELISA Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN2464133
  • Target See all Huntingtin (HTT) Antibodies
    Huntingtin (HTT)
    Binding Specificity
    • 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
    Reactivity
    • 63
    • 45
    • 36
    • 6
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Human, Rat, Mouse
    Host
    • 60
    • 21
    • 2
    Rabbit
    Clonality
    • 53
    • 29
    Polyclonal
    Conjugate
    • 55
    • 3
    • 3
    • 3
    • 3
    • 3
    • 3
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This Huntingtin antibody is un-conjugated
    Application
    • 40
    • 32
    • 24
    • 14
    • 14
    • 13
    • 13
    • 9
    • 7
    • 4
    • 4
    • 2
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC), ELISA
    Purification
    Affinity Purified
    Immunogen
    A synthetic peptide corresponding to the N-terminus.
    Isotype
    IgG
    Top Product
    Discover our top product HTT Primary Antibody
  • Application Notes
    ELISA, Western (immuno) blotting, Immunostaining (in testing)
    Restrictions
    For Research Use only
  • Target
    Huntingtin (HTT)
    Alternative Name
    Huntington Protein (HTT Products)
    Synonyms
    HTT antibody, hd antibody, ZHD antibody, CG9995 antibody, Dmel\\CG9995 antibody, HD antibody, Hsap\\HD antibody, Htt antibody, dHtt antibody, dhtt antibody, SLC6A4 antibody, huntington antibody, it15 antibody, htt antibody, IT15 antibody, AI256365 antibody, C430023I11Rik antibody, Hd antibody, Hdh antibody, huntingtin antibody, HTT antibody, htt antibody, LOC373520 antibody, Htt antibody
    Background
    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.
    Gene ID
    3064
    UniProt
    P42858
    Pathways
    PI3K-Akt Signaling, Hormone Transport, Transition Metal Ion Homeostasis, Tube Formation, Protein targeting to Nucleus, Dicarboxylic Acid Transport
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