TMEM166 抗体
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- 抗原 See all TMEM166 (FAM176A) 抗体
- TMEM166 (FAM176A) (Family with Sequence Similarity 176, Member A (FAM176A))
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适用
- 人, 小鼠
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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 TMEM166 antibody is un-conjugated
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应用范围
- Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
- 产品特性
- Polyclonal Antibody
- 纯化方法
- Affinity purification
- 免疫原
- Synthetic peptide of human EVA1A
- 亚型
- IgG
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anti-Family with Sequence Similarity 176, Member A (FAM176A) (AA 58-152) antibody
FAM176A 适用: 人 ELISA, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Family with Sequence Similarity 176, Member A (FAM176A) (AA 104-137) antibodyFAM176A 适用: 斑马鱼 WB 宿主: 兔 Polyclonal RB51996 unconjugated
anti-Family with Sequence Similarity 176, Member A (FAM176A) (AA 51-100) antibodyFAM176A 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Family with Sequence Similarity 176, Member A (FAM176A) (N-Term) antibodyFAM176A 适用: 人, 小鼠, 犬, 马, Pig, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-Family with Sequence Similarity 176, Member A (FAM176A) (N-Term) antibodyFAM176A 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Family with Sequence Similarity 176, Member A (FAM176A) (Middle Region) antibodyFAM176A 适用: 人, 犬, 马, 兔, Pig WB 宿主: 兔 Polyclonal unconjugated
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- 应用备注
- WB 1:200-1:1000, IHC 1:25-1:100
- 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 0.7 mg/mL
- 缓冲液
- PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
- 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
- -20 °C
- 储存方法
- Store at -20°C. Avoid freeze / thaw cycles.
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- 抗原
- TMEM166 (FAM176A) (Family with Sequence Similarity 176, Member A (FAM176A))
- 别名
- EVA1A (FAM176A 产品)
- 背景
- TMEM166, also known as FAM176A (family with sequence similarity 176, member A), is a 152 amino acid protein encoded by a gene mapping to human chromosome 2. The second largest human chromosome, 2 consists of 237 million bases encoding over 1,400 genes and making up approximately 8 % of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated witHuman, Mouseutations in the ABCA12 gene.
- 分子量
- 17 kDa
- NCBI登录号
- NP_115557
- UniProt
- Q9H8M9
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