RNF148 抗体
Quick Overview for RNF148 抗体 (ABIN7239431)
抗原
适用
宿主
克隆类型
标记
应用范围
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产品特性
- Polyclonal Antibody
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纯化方法
- Affinity purification
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免疫原
- Synthetic peptide of human RNF148
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亚型
- IgG
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anti-Ring Finger Protein 148 (RNF148) (AA 208-305) antibody
RNF148 适用: 人 ELISA, IHC, WB, IF 宿主: 兔 Polyclonal unconjugated
anti-Ring Finger Protein 148 (RNF148) (AA 139-238) antibodyRNF148 适用: 人 ELISA, WB 宿主: 小鼠 Monoclonal 2D3 unconjugated
anti-Ring Finger Protein 148 (RNF148) antibodyRNF148 适用: 人, 小鼠 ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Ring Finger Protein 148 (RNF148) (AA 218-267) antibodyRNF148 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
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应用备注
- IHC 1:50-1:200
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 0.8 mg/mL
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缓冲液
- PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
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储存液
- Sodium azide
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注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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储存条件
- -20 °C
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储存方法
- Store at -20°C. Avoid freeze / thaw cycles.
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- RNF148 (Ring Finger Protein 148 (RNF148))
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别名
- RNF148
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背景
- RNF148 (RING finger protein 148) is a 305 amino acid single-pass membrane protein that contains one PA (protease associated) domain and a single RING-type zinc finger. RNF148 is encoded by a gene that maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5 % of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance.
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NCBI登录号
- NP_932351
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UniProt
- Q8N7C7
抗原
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