电话:
+86 (0512) 65829739
传真:
+86 (010) 6788 5057
电子邮件:
orders@antibodies-online.cn

NLRP2 抗体 (AA 701-751)

NLRP2 适用: 小鼠 WB, IP 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7451888
发货至: 中国
  • 抗原 See all NLRP2 抗体
    NLRP2 (NLR Family, Pyrin Domain Containing 2 (NLRP2))
    抗原表位
    • 4
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 701-751
    适用
    • 32
    • 8
    • 5
    • 1
    • 1
    小鼠
    宿主
    • 24
    • 5
    • 2
    • 1
    克隆类型
    • 28
    • 4
    多克隆
    标记
    • 32
    This NLRP2 antibody is un-conjugated
    应用范围
    • 29
    • 10
    • 6
    • 6
    • 4
    • 3
    • 2
    • 2
    • 1
    • 1
    Western Blotting (WB), Immunoprecipitation (IP)
    原理
    Rabbit anti-NBS1 Antibody, Affinity Purified
    预测反应
    Rat
    纯化方法
    Affinity Purified
    免疫原
    between AA 701 and 751
    亚型
    IgG
    Top Product
    Discover our top product NLRP2 Primary Antibody
  • 应用备注

    IP: 2 - 5 μg/mg lysate

    WB: 1:2,000 - 1:10,000

    限制
    仅限研究用
  • 浓度
    200 μg/mL
    缓冲液
    Tris-buffered Saline containing 0.1 % BSA and 0.09 % Sodium Azide
    储存液
    Sodium azide
    注意事项
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    储存条件
    4 °C
    有效期
    12 months
  • 抗原
    NLRP2 (NLR Family, Pyrin Domain Containing 2 (NLRP2))
    别名
    NBS1 (NLRP2 产品)
    别名
    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
    背景
    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.
    基因ID
    27354
    NCBI登录号
    NP_038780
    UniProt
    Q9R207
    途径
    Production of Molecular Mediator of Immune Response, Positive Regulation of Endopeptidase Activity, Inflammasome
You are here:
客服