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IFRD1 antibody

IFRD1 Reactivity: Human, Mouse, Rat WB, ELISA Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN5699283
  • Target See all IFRD1 Antibodies
    IFRD1 (Interferon Related Developmental Regulator 1 (IFRD1))
    Reactivity
    • 29
    • 11
    • 10
    • 5
    • 5
    • 4
    • 4
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    Human, Mouse, Rat
    Host
    • 27
    • 2
    Rabbit
    Clonality
    • 29
    Polyclonal
    Conjugate
    • 20
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This IFRD1 antibody is un-conjugated
    Application
    • 17
    • 9
    • 8
    • 7
    • 2
    • 2
    • 1
    Western Blotting (WB), ELISA
    Immunogen
    interferon-related developmental regulator 1
    Isotype
    IgG
    Top Product
    Discover our top product IFRD1 Primary Antibody
  • Application Notes
    Optimal working dilution should be determined by the investigator.
    Restrictions
    For Research Use only
  • Buffer
    PBS with 0.02 % sodium azide and 50 % glycerol  pH 7.3
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Handling Advice
    Avoid repeated freeze / thaw cycles.
    Storage
    -20 °C
    Expiry Date
    12 months
  • Target
    IFRD1 (Interferon Related Developmental Regulator 1 (IFRD1))
    Alternative Name
    IFRD1 (IFRD1 Products)
    Synonyms
    im:7067566 antibody, si:dkey-192l17.2 antibody, wu:fi35f04 antibody, wu:fj67a06 antibody, zgc:154080 antibody, IFR1 antibody, PC4 antibody, TIS7 antibody, Ifnl antibody, Tis7 antibody, Pc4 antibody, interferon-related developmental regulator 1 antibody, interferon related developmental regulator 1 L homeolog antibody, interferon related developmental regulator 1 antibody, ifrd1 antibody, ifrd1.L antibody, IFRD1 antibody, Ifrd1 antibody
    Background
    Synonyms: Background:This gene is an immediate early gene that encodes a protein related to interferon-gamma. This protein may function as a transcriptional co-activator/repressor that controls the growth and differentiation of specific cell types during embryonic development and tissue regeneration. Mutations in this gene are associated with sensory/motor neuropathy with ataxia. This gene may also be involved in modulating the pathogenesis of cystic fibrosis lung disease. Alternate splicing results in multiple transcript variants.
    Molecular Weight
    51 kDa
    Gene ID
    3475
    UniProt
    O00458
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