NLRP2 抗体 (AA 625-675)
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- 抗原 See all NLRP2 抗体
- NLRP2 (NLR Family, Pyrin Domain Containing 2 (NLRP2))
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抗原表位
- AA 625-675
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适用
- 人
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This NLRP2 antibody is un-conjugated
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应用范围
- Western Blotting (WB), Immunoprecipitation (IP)
- 原理
- Rabbit anti-NBS1 Antibody, Affinity Purified
- 纯化方法
- Affinity Purified
- 免疫原
- between AA 625 and 675
- 亚型
- IgG
- Top Product
- Discover our top product NLRP2 Primary Antibody
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- 应用备注
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IP: 2 - 10 μg/mg lysate
WB: 1:1,000 - 1:10,000
- 限制
- 仅限研究用
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- 浓度
- 1000 μg/mL
- 缓冲液
- Tris-citrate/phosphate buffer, pH 7 to 8 containing 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
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- 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
- 4683
- NCBI登录号
- NP_002476
- UniProt
- O60934
- 途径
- Production of Molecular Mediator of Immune Response, Positive Regulation of Endopeptidase Activity, Inflammasome
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