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TINF2 antibody

TIN2 Reactivity: Human WB Host: Rabbit Monoclonal unconjugated
Catalog No. ABIN7270771
  • Target See all TINF2 (TIN2) Antibodies
    TINF2 (TIN2) (TERF1 Interacting Nuclear Factor 2 (TIN2))
    Reactivity
    • 20
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    Human
    Host
    • 16
    • 5
    Rabbit
    Clonality
    • 18
    • 3
    Monoclonal
    Conjugate
    • 17
    • 2
    • 1
    • 1
    This TINF2 antibody is un-conjugated
    Application
    • 16
    • 13
    • 5
    • 2
    • 1
    • 1
    Western Blotting (WB)
    Purpose
    TIN2/TINF2 Rabbit mAb
    Cross-Reactivity
    Human, Mouse, Rat
    Characteristics
    Monoclonal Antibodies
    Purification
    Affinity purification
    Immunogen
    A synthesized peptide derived from human TIN2/TINF2
    Isotype
    IgG
    Top Product
    Discover our top product TIN2 Primary Antibody
  • Application Notes
    WB,1:500 - 1:2000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    PBS with 0.02 % sodium azide,0.05 % BSA,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.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    TINF2 (TIN2) (TERF1 Interacting Nuclear Factor 2 (TIN2))
    Alternative Name
    TINF2 (TIN2 Products)
    Synonyms
    DKCA3 antibody, TIN2 antibody, AW552114 antibody, D14Wsu146e antibody, Tin2 antibody, TERF1 interacting nuclear factor 2 antibody, Terf1 (TRF1)-interacting nuclear factor 2 antibody, TINF2 antibody, Tinf2 antibody
    Background
    This gene encodes one of the proteins of the shelterin, or telosome, complex which protects telomeres by allowing the cell to distinguish between telomeres and regions of DNA damage. The protein encoded by this gene is a critical part of shelterin, it interacts with the three DNA-binding proteins of the shelterin complex, and it is important for assembly of the complex. Mutations in this gene cause dyskeratosis congenita (DKC), an inherited bone marrow failure syndrome. [provided by RefSeq, Mar 2010],DKCA3, TIN2,Epigenetics & Nuclear Signaling,TINF2
    Molecular Weight
    40kDa
    Gene ID
    26277
    UniProt
    Q9BSI4
    Pathways
    Cell Division Cycle, Telomere Maintenance, Regulation of Carbohydrate Metabolic Process
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