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Neurofibromin 1 antibody (AA 160-270)

This Rabbit Polyclonal antibody specifically detects Neurofibromin 1 in ELISA, WB, IF, IHC (p) and FACS. It exhibits reactivity toward Human.
Catalog No. ABIN7871102
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for Neurofibromin 1 antibody (AA 160-270) (ABIN7871102)

Target

See all Neurofibromin 1 (NF1) Antibodies
Neurofibromin 1 (NF1)

Reactivity

  • 70
  • 56
  • 38
  • 2
  • 2
  • 2
  • 2
  • 1
Human

Host

  • 76
  • 10
Rabbit

Clonality

  • 74
  • 12
Polyclonal

Conjugate

  • 34
  • 5
  • 4
  • 4
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Neurofibromin 1 antibody is un-conjugated

Application

  • 39
  • 39
  • 27
  • 26
  • 16
  • 14
  • 12
  • 9
  • 9
  • 7
  • 5
  • 1
ELISA, Western Blotting (WB), Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Flow Cytometry (FACS)
  • Binding Specificity

    • 15
    • 15
    • 15
    • 5
    • 5
    • 4
    • 3
    • 3
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 160-270

    Purpose

    Neurofibromin Antibody / NF1

    Purification

    Affinity purified

    Immunogen

    Recombinant human protein (amino acids R160-Q270) was used as the immunogen for the Neurofibromin antibody.

    Isotype

    IgG
  • Application Notes

    Optimal dilution of the Neurofibromin antibody should be determined by the researcher.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Storage

    4 °C,-20 °C

    Storage Comment

    After reconstitution, the Neurofibromin antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • Target

    Neurofibromin 1 (NF1)

    Alternative Name

    Neurofibromin

    Background

    Neurofibromin 1 (NF1) is a gene in humans that is located on chromosome 17. This gene product appears to function as a negative regulator of the ras signal transduction pathway. Mutations in this gene have been linked to neurofibromatosis type 1, juvenile myelomonocytic leukemia and Watson syndrome. The mRNA for this gene is subject to RNA editing (CGA>UGA->Arg1306Term) resulting in premature translation termination. Alternatively spliced transcript variants encoding different isoforms have also been described for this gene.

    UniProt

    P21359

    Pathways

    cAMP Metabolic Process, Regulation of long-term Neuronal Synaptic Plasticity
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