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NLRP2 antibody (AA 625-675)

NLRP2 Reactivity: Human WB, IP Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7449676
  • Target See all NLRP2 Antibodies
    NLRP2 (NLR Family, Pyrin Domain Containing 2 (NLRP2))
    Binding Specificity
    • 4
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 625-675
    Reactivity
    • 31
    • 9
    • 5
    • 1
    • 1
    Human
    Host
    • 24
    • 5
    • 2
    • 1
    Rabbit
    Clonality
    • 28
    • 4
    Polyclonal
    Conjugate
    • 32
    This NLRP2 antibody is un-conjugated
    Application
    • 29
    • 10
    • 6
    • 6
    • 4
    • 3
    • 2
    • 2
    • 1
    • 1
    Western Blotting (WB), Immunoprecipitation (IP)
    Purpose
    Rabbit anti-NBS1 Antibody, Affinity Purified
    Purification
    Affinity Purified
    Immunogen
    between AA 625 and 675
    Isotype
    IgG
    Top Product
    Discover our top product NLRP2 Primary Antibody
  • Application Notes

    IP: 2 - 10 μg/mg lysate

    WB: 1:1,000 - 1:10,000

    Restrictions
    For Research Use only
  • Concentration
    1000 μg/mL
    Buffer
    Tris-citrate/phosphate buffer, pH 7 to 8 containing 0.09 % Sodium Azide
    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
    4 °C
    Expiry Date
    12 months
  • Target
    NLRP2 (NLR Family, Pyrin Domain Containing 2 (NLRP2))
    Alternative Name
    NBS1 (NLRP2 Products)
    Synonyms
    CLR19.9 antibody, NALP2 antibody, NBS1 antibody, PAN1 antibody, PYPAF2 antibody, NLRP2 antibody, E330007A02Rik antibody, Nalp2 antibody, NLR family pyrin domain containing 2 antibody, NACHT, LRR and PYD domains-containing protein 2 antibody, NLR family pyrin domain containing 7 antibody, NLR family, pyrin domain containing 2 antibody, NLRP2 antibody, LOC100301026 antibody, LOC100387349 antibody, NLRP7 antibody, Nlrp2 antibody
    Background
    Background: Mutations in NBS1 (Nijmegen Breakage Syndrome 1), also known as nibrin, are associated with the autosomal recessive syndrome, Nijmegen breakage syndrome, characterized by microcephaly, growth retardation, immunodeficiency, and cancer predisposition. At the cellular level, NBS1 is part of the MRE11/RAD50 double-strand break repair complex that is critical to the DNA damage response, DNA recombination, telomere integrity, and cell cycle checkpoint control.
    Gene ID
    4683
    NCBI Accession
    NP_002476
    UniProt
    O60934
    Pathways
    Production of Molecular Mediator of Immune Response, Positive Regulation of Endopeptidase Activity, Inflammasome
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