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SNX29 antibody

RUNDC2A Reactivity: Human IHC, ELISA Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7192586
  • Target See all SNX29 (RUNDC2A) products
    SNX29 (RUNDC2A) (RUN Domain Containing 2A (RUNDC2A))
    Reactivity
    • 30
    • 4
    • 4
    • 4
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Human
    Host
    • 28
    • 2
    Rabbit
    Clonality
    • 28
    • 2
    Polyclonal
    Conjugate
    • 13
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This SNX29 antibody is un-conjugated
    Application
    • 22
    • 18
    • 16
    • 3
    • 2
    Immunohistochemistry (IHC), ELISA
    Cross-Reactivity
    Human, Mouse
    Purification
    Antigen affinity purification
    Immunogen
    Synthetic peptide of Human SNX29
    Isotype
    IgG
  • Application Notes
    ELISA:1:1000-1:2000, IHC:1:20-1:100,
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    -20 °C, pH 7.4 PBS, 0.05 % Sodium azide, 40 % Glycerol
    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,-80 °C
    Storage Comment
    Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
  • Target
    SNX29 (RUNDC2A) (RUN Domain Containing 2A (RUNDC2A))
    Alternative Name
    SNX29 (RUNDC2A Products)
    Synonyms
    RUNDC2A antibody, 4933437K13Rik antibody, ENSMUSG00000079738 antibody, Gm11170 antibody, Gm1737 antibody, Gm930 antibody, Rundc2a antibody, RGD1565890 antibody, A-388D4.1 antibody, RUN domain containing 2A antibody, sorting nexin 29 antibody, sorting nexin-29 antibody, RUNDC2A antibody, Snx29 antibody, SNX29 antibody, LOC104975843 antibody
    Background

    Background: SNX29 also known as RUNDC2A, is a 375 amino protein that contains one RUN domain. RUNDC2A is encoded by a gene that maps to human chromosome 16p13.13, which encodes over 900 genes and comprises nearly 3 % of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, as is Crohn's disease, which is a gastrointestinal inflammatory condition.

    Aliases: SNX29 antibody, RUNDC2A antibody, Sorting nexin-29 antibody, RUN domain-containing protein 2A antibody

    UniProt
    Q8TEQ0
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