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Nibrin antibody

NBN Reactivity: Human, Mouse WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN5963855
  • Target See all Nibrin (NBN) Antibodies
    Nibrin (NBN)
    Reactivity
    • 100
    • 62
    • 36
    • 2
    • 1
    • 1
    • 1
    • 1
    Human, Mouse
    Host
    • 119
    • 15
    Rabbit
    Clonality
    • 109
    • 25
    Polyclonal
    Conjugate
    • 68
    • 8
    • 6
    • 6
    • 6
    • 6
    • 6
    • 6
    • 5
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    This Nibrin antibody is un-conjugated
    Application
    • 105
    • 45
    • 28
    • 27
    • 26
    • 26
    • 25
    • 17
    • 10
    • 9
    • 6
    • 4
    • 2
    • 2
    • 1
    Western Blotting (WB)
    Purification
    Affinity purification
    Immunogen
    A synthetic peptide of human NBN
    Isotype
    IgG
    Top Product
    Discover our top product NBN Primary Antibody
  • Application Notes
    WB 1:500 - 1:1000
    Restrictions
    For Research Use only
  • Concentration
    1 mg/mL
    Buffer
    Buffer: PBS with 0.02 % sodium azide, 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
    Nibrin (NBN)
    Alternative Name
    NBN (NBN Products)
    Synonyms
    NBN antibody, AT-V1 antibody, AT-V2 antibody, ATV antibody, NBS antibody, NBS1 antibody, P95 antibody, Nbs1 antibody, im:6911679 antibody, zgc:194152 antibody, nibrin antibody, NBN antibody, nbn antibody, Nbn antibody
    Background

    Synonyms: AT V1,AT V2,ATV,Cell cycle regulatory protein p95,FLJ10155,MGC87362,Nbn,NBN,NBS 1,NBS,NBS1,Nibrin,Nijmegen breakage syndrome 1 (nibrin),Nijmegen breakage syndrome,Nijmegen breakage syndrome protein 1,p95,p95 protein of the MRE11/RAD50 complex

    Background: Mutations in this gene are associated with Nijmegen breakage syndrome, an autosomal recessive chromosomal instability syndrome characterized by microcephaly, growth retardation, immunodeficiency, and cancer predisposition. The encoded protein is a member of the MRE11/RAD50 double-strand break repair complex which consists of 5 proteins. This gene product is thought to be involved in DNA double-strand break repair and DNA damage-induced checkpoint activation.

    Molecular Weight

    Observed_MW: 95kDa

    Calculated_MW: 84kDa

    Gene ID
    4683
    UniProt
    O60934
    Pathways
    DNA Damage Repair, Production of Molecular Mediator of Immune Response
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