SNX29 抗体
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- 抗原 See all SNX29 (RUNDC2A) products
- SNX29 (RUNDC2A) (RUN Domain Containing 2A (RUNDC2A))
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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 SNX29 antibody is un-conjugated
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应用范围
- Immunohistochemistry (IHC), ELISA
- 交叉反应
- 人, 小鼠
- 纯化方法
- Antigen affinity purification
- 免疫原
- Synthetic peptide of Human SNX29
- 亚型
- IgG
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- 应用备注
- ELISA:1:1000-1:2000, IHC:1:20-1:100,
- 限制
- 仅限研究用
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- 状态
- Liquid
- 缓冲液
- -20 °C, pH 7.4 PBS, 0.05 % Sodium azide, 40 % Glycerol
- 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,-80 °C
- 储存方法
- Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
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- 抗原
- SNX29 (RUNDC2A) (RUN Domain Containing 2A (RUNDC2A))
- 别名
- SNX29 (RUNDC2A 产品)
- 别名
- RUNDC2A antibody, 4933437K13Rik antibody, ENSMUSG00000079738 antibody, Gm11170 antibody, Gm1737 antibody, Gm930 antibody, Rundc2a antibody, RGD1565890 antibody, A-388D4.1 antibody, RUN domain containing 2A antibody, sorting nexin 29 antibody, sorting nexin-29 antibody, RUNDC2A antibody, Snx29 antibody, SNX29 antibody, LOC104975843 antibody
- 背景
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Background: SNX29 also known as RUNDC2A, is a 375 amino protein that contains one RUN domain. RUNDC2A is encoded by a gene that maps to human chromosome 16p13.13, which encodes over 900 genes and comprises nearly 3 % of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, as is Crohn's disease, which is a gastrointestinal inflammatory condition.
Aliases: SNX29 antibody, RUNDC2A antibody, Sorting nexin-29 antibody, RUN domain-containing protein 2A antibody
- UniProt
- Q8TEQ0
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