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Nibrin antibody

The Mouse Monoclonal anti-Nibrin antibody has been validated for WB, IF, ICC and IP. It is suitable to detect Nibrin in samples from Human.
Catalog No. ABIN7464244

Quick Overview for Nibrin antibody (ABIN7464244)

Target

See all Nibrin (NBN) Antibodies
Nibrin (NBN)

Reactivity

  • 94
  • 61
  • 35
  • 2
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 112
  • 14
Mouse

Clonality

  • 99
  • 27
Monoclonal

Conjugate

  • 69
  • 7
  • 5
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
This Nibrin antibody is un-conjugated

Application

  • 104
  • 42
  • 30
  • 29
  • 27
  • 26
  • 22
  • 16
  • 14
  • 11
  • 6
  • 4
  • 2
  • 2
  • 1
Western Blotting (WB), Immunofluorescence (IF), Immunocytochemistry (ICC), Immunoprecipitation (IP)

Grade

KO Validated

Clone

1C3
  • Cross-Reactivity

    Human, Mouse

    Purification

    Protein G purified

    Immunogen

    The complete coding region of the human p95/NBS1 expressed in E. coli.

    Isotype

    IgG1
  • Application Notes

    WB: 1:500-1:3000. ICC/IF: 1:100. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

    Comment

    Positive Control: 293T , MCF7 , HeLa , Raji

    Validation: KO/KD, Orthogonal

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    1XPBS ( pH 7), 20 % Glycerol, No Preservative

    Preservative

    Without preservative

    Storage

    4 °C,-20 °C

    Storage Comment

    Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
  • Target

    Nibrin (NBN)

    Alternative Name

    nibrin

    Background

    Nibrin , AT-V1 , AT-V2 , ATV , NBS , NBS1 , P95,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. [provided by RefSeq, Jul 2008]

    Molecular Weight

    85 kDa

    Gene ID

    4683

    UniProt

    O60934

    Pathways

    DNA Damage Repair, Production of Molecular Mediator of Immune Response
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