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C16orf45 antibody

C16orf45 Reactivity: Human, Mouse, Rat ELISA, IHC Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7244585
  • Target See all C16orf45 products
    C16orf45 (Chromosome 16 Open Reading Frame 45 (C16orf45))
    Reactivity
    Human, Mouse, Rat
    Host
    • 16
    Rabbit
    Clonality
    • 16
    Polyclonal
    Conjugate
    • 4
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This C16orf45 antibody is un-conjugated
    Application
    • 9
    • 7
    • 7
    • 2
    • 1
    ELISA, Immunohistochemistry (IHC)
    Characteristics
    Polyclonal Antibody
    Purification
    Antigen affinity purification
    Immunogen
    Synthetic peptide of human C16orf45
    Isotype
    IgG
  • Application Notes
    IHC 1:30-1:150, ELISA 1:5000-1:10000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.7 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
    C16orf45 (Chromosome 16 Open Reading Frame 45 (C16orf45))
    Alternative Name
    C16orf45 (C16orf45 Products)
    Synonyms
    C16orf45 antibody, chromosome 16 open reading frame 45 antibody, RIKEN cDNA 2900011O08 gene antibody, similar to RIKEN cDNA 2900011O08 antibody, chromosome 16 open reading frame, human C16orf45 antibody, chromosome 25 open reading frame, human C16orf45 antibody, C16orf45 antibody, 2900011O08Rik antibody, RGD1305733 antibody, C16H16orf45 antibody, C25H16orf45 antibody
    Background
    C16orf45, also known as FLJ32618, is a 204 amino acid protein encoded by a gene mapping to human chromosome 16. Chromosome 16 encodes over 900 genes in approximately 90 million base pairs, makes up nearly 3 % of human cellular DNA and is associated with a variety of genetic disorders. 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, though through the CREBBP gene which encodes a critical CREB binding protein. Signs of Rubinstein-Taybi include mental retardation and predisposition to tumor growth and white blood cell neoplasias. Crohn's disease is a gastrointestinal inflammatory condition associated with chromosome 16 through the NOD2 gene. An association with systemic lupus erythematosis and a number of other autoimmune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier.
    UniProt
    Q96MC5
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