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Huntingtin antibody (N-Term)

This anti-Huntingtin antibody is a Rabbit Polyclonal antibody detecting Huntingtin in WB, ELISA and ICC. Suitable for Human, Rat and Mouse.
Catalog No. ABIN4889208

Quick Overview for Huntingtin antibody (N-Term) (ABIN4889208)

Target

See all Huntingtin (HTT) Antibodies
Huntingtin (HTT)

Reactivity

  • 63
  • 48
  • 41
  • 6
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human, Rat, Mouse

Host

  • 60
  • 24
  • 2
Rabbit

Clonality

  • 51
  • 34
Polyclonal

Conjugate

  • 65
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Huntingtin antibody is un-conjugated

Application

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  • 20
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  • 11
  • 9
  • 8
  • 4
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  • 1
Western Blotting (WB), ELISA, Immunocytochemistry (ICC)
  • Binding Specificity

    • 15
    • 5
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    • 4
    • 3
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    • 2
    • 2
    • 2
    • 2
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    • 1
    • 1
    • 1
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    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    N-Term

    Specificity

    Reacts with the human Huntingtin protein

    Cross-Reactivity

    Mouse (Murine), Rat (Rattus)

    Cross-Reactivity (Details)

    Cross react with mouse and rat protein due to sequence homology.

    Purification

    Purified (protein A)

    Immunogen

    synthetic peptide derived from N terminal part of human Huntingtin
  • Application Notes

    Working dilution: Optimal dilutions should be determined by the end user.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Must be reconstituted in distilled water.

    Concentration

    1 mg/mL

    Buffer

    Tris 0,1M, glycine 0,1M, sucrose 2 %

    Storage

    4 °C/-20 °C

    Storage Comment

    Lyophilized powder stable for a minimum of 2 years at -20°C. Store reconstituted antibodies at +4°C. For extended periods store in aliquots at -20°C. Antibodies are guaranteed for 6 month from date of receipt.

    Expiry Date

    24 months
  • Target

    Huntingtin (HTT)

    Alternative Name

    Huntingtin

    Background

    Defects in HTT are the cause of Huntington disease (HD). HD is an autosomal dominant neurodegenerative disorder characterized by involuntary movements (chorea), general motor impairment, psychiatric disorders and dementia.

    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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