TMEM199 抗体 (AA 20-129)
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- 抗原 See all TMEM199 products
- TMEM199 (Transmembrane Protein 199 (TMEM199))
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抗原表位
- AA 20-129
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适用
- 人, 小鼠, 大鼠
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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 TMEM199 antibody is un-conjugated
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应用范围
- Western Blotting (WB), ELISA
- 原理
- Rabbit IgG polyclonal antibody for TMEM199 detection. Tested with WB, Direct ELISA in Human,Mouse,Rat.
- 交叉反应 (详细)
- No cross reactivity with other proteins.
- 产品特性
- Rabbit IgG polyclonal antibody for TMEM199 detection. Tested with WB, Direct ELISA in Human,Mouse,Rat.
- 纯化方法
- Immunogen affinity purified.
- 免疫原
- E.coli-derived human TMEM199 recombinant protein (Position: E20-H129).
- 亚型
- IgG
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- 应用备注
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Application details: Western blot|0.1-0.5 μg/mL Direct ELISA|0.1-0.5 μg/mL
- 说明
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Tested Species: In-house tested species with positive results. Other applications have not been tested. Optimal dilutions should be determined by end users.
- 限制
- 仅限研究用
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- 状态
- Lyophilized
- 溶解方式
- Add 0.2 mL of distilled water will yield a concentration of 500 μg/mL.
- 缓冲液
- Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4, 0.05 mg 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,-20 °C
- 储存方法
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At -20°C for one year. After reconstitution, at 4°C for one month.
It can also be aliquotted and stored frozen at -20 °C for a longer time. Avoid repeated freezing and thawing.
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- 抗原
- TMEM199 (Transmembrane Protein 199 (TMEM199))
- 别名
- TMEM199 (TMEM199 产品)
- 别名
- C17orf32 antibody, AI316787 antibody, AI848469 antibody, R74819 antibody, transmembrane protein 199 antibody, TMEM199 antibody, Tmem199 antibody
- 背景
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Synonyms: Transmembrane protein 199, TMEM199, C17orf32
Background: TMEM199 encodes a protein homologous to the yeast V-ATPase assembly factor Vma12 and appears to be involved in Golgi homeostasis. The protein encoded by this gene has been observed to localize to the endoplasmic reticulum (ER)-Golgi intermediate compartment (ERGIC) and coat protein complex I (COPI) in some human cells. Defects in this gene are a cause of congenital disorder of glycosylation, type IIp. By genomic sequence analysis, the TMEM199 gene is mapped to chromosome 17q11.1.
- 基因ID
- 147007
- UniProt
- Q8N511
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