NDRG1 抗体 (AA 1-394)
Quick Overview for NDRG1 抗体 (AA 1-394) (ABIN5776094)
抗原
See all NDRG1 抗体适用
宿主
克隆类型
标记
应用范围
克隆位点
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抗原表位
- AA 1-394
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免疫原
- Recombinant human NDRG1 (1-394aa) purified from E. coli
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亚型
- IgG1 kappa
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anti-N-Myc Downstream Regulated 1 (NDRG1) (C-Term) antibody
Verified NDRG1 适用: 人 WB, ELISA, IHC 宿主: 山羊 Polyclonal unconjugated
anti-N-Myc Downstream Regulated 1 (NDRG1) (AA 1-394) antibodyNDRG1 适用: 人 WB, ELISA, IF, IHC (p) 宿主: 小鼠 Monoclonal 2D7 unconjugated
anti-N-Myc Downstream Regulated 1 (NDRG1) antibodyNDRG1 适用: 人 WB, IHC 宿主: 兔 Monoclonal unconjugated
anti-N-Myc Downstream Regulated 1 (NDRG1) (AA 12-40) antibodyNDRG1 适用: 人 WB, ELISA, IHC, FACS 宿主: 兔 Polyclonal unconjugated
anti-N-Myc Downstream Regulated 1 (NDRG1) (AA 136-394) antibodyNDRG1 适用: 人 WB, ELISA, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-N-Myc Downstream Regulated 1 (NDRG1) antibodyNDRG1 适用: 人 WB, ELISA, IHC, IF 宿主: 兔 Monoclonal 4C8 unconjugated Recombinant Antibody
anti-N-Myc Downstream Regulated 1 (NDRG1) antibodyNDRG1 适用: 人, 小鼠, 大鼠 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-N-Myc Downstream Regulated 1 (NDRG1) (AA 175-394) antibodyNDRG1 适用: 人 WB, IF 宿主: 兔 Polyclonal unconjugated
anti-N-Myc Downstream Regulated 1 (NDRG1) antibodyNDRG1 适用: 人 WB, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-N-Myc Downstream Regulated 1 (NDRG1) (AA 12-40), (N-Term) antibodyNDRG1 适用: 人 WB, FACS, IHC (p) 宿主: 兔 Polyclonal RB21832 unconjugated
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 1 mg/mL
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储存条件
- 4 °C,-20 °C,-80 °C
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储存方法
- Can be stored at +2°C to +8°C for 1 week. For long term storage, aliquot and store at -20°C to -80°C. Avoid repeated freezing and thawing cycles.
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- NDRG1 (N-Myc Downstream Regulated 1 (NDRG1))
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别名
- NDRG1
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背景
- N-myc downstream regulated gene (NDRG) -1 is one of 4 members of the NDRG alpha/beta-hydrolase family. This protein is classified in databases as a tumor suppressor and heavy metal-response protein. Its functions include cell-cycle regulation, cellular differentiation, apoptosis, hypoxia response and metal-ion sensing. Mutation in the NDRG1 gene has been reported to be causative for hereditary motor and sensory neuropathy-Lom (HMSNL), a severe autosomal recessive form of Charcot-Marie-Tooth (CMT) disease.
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NCBI登录号
- NP_006087
抗原
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