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RTN4IP1 antibody

RTN4IP1 Reactivity: Human, Mouse ELISA, IHC Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7244687
  • Target See all RTN4IP1 Antibodies
    RTN4IP1 (Reticulon 4 Interacting Protein 1 (RTN4IP1))
    Reactivity
    • 32
    • 16
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    Human, Mouse
    Host
    • 44
    • 3
    Rabbit
    Clonality
    • 46
    • 1
    Polyclonal
    Conjugate
    • 13
    • 5
    • 4
    • 4
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    This RTN4IP1 antibody is un-conjugated
    Application
    • 36
    • 19
    • 15
    • 14
    • 13
    • 13
    • 7
    • 3
    • 1
    ELISA, Immunohistochemistry (IHC)
    Characteristics
    Polyclonal Antibody
    Purification
    Antigen affinity purification
    Immunogen
    Synthetic peptide of human RTN4IP1
    Isotype
    IgG
    Top Product
    Discover our top product RTN4IP1 Primary Antibody
  • Application Notes
    IHC 1:40-1:200, ELISA 1:5000-1:10000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1.2 mg/mL
    Buffer
    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    RTN4IP1 (Reticulon 4 Interacting Protein 1 (RTN4IP1))
    Alternative Name
    RTN4IP1 (RTN4IP1 Products)
    Synonyms
    RTN4IP1 antibody, NIMP antibody, D10Ertd690e antibody, RGD1563384 antibody, reticulon 4 interacting protein 1 antibody, RTN4IP1 antibody, Rtn4ip1 antibody
    Background
    This gene encodes a mitochondrial protein that interacts with reticulon 4, which is a potent inhibitor of regeneration following spinal cord injury. This interaction may be important for reticulon-induced inhibition of neurite growth. Mutations in this gene can cause optic atrophy 10, with or without ataxia, mental retardation, and seizures. There is a pseudogene for this gene on chromosome 12. Alternative splicing results in multiple transcript variants.
    UniProt
    Q8WWV3
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