UFD1L 抗体 (AA 208-307)
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- 抗原 See all UFD1L 抗体
- UFD1L (Ubiquitin Fusion Degradation Protein 1 Homolog (UFD1L))
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抗原表位
- AA 208-307
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适用
- 人
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宿主
- 小鼠
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克隆类型
- 单克隆
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标记
- This UFD1L antibody is un-conjugated
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应用范围
- Western Blotting (WB), Immunohistochemistry (IHC), ELISA, Immunocytochemistry (ICC), Flow Cytometry (FACS)
- 原理
- UFD1L Antibody
- 纯化方法
- Purified antibody
- 免疫原
- Purified recombinant fragment of human UFD1L (AA: 208-307) expressed in E. Coli.
- 克隆位点
- 2A6F3
- 亚型
- IgG2b
- Top Product
- Discover our top product UFD1L Primary Antibody
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- 应用备注
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ELISA: 1/10000
FCM: 1/200 - 1/400
ICC: 1/200 - 1/1000
- 限制
- 仅限研究用
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- 状态
- Liquid
- 缓冲液
- Purified antibody in PBS with 0.05 % 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
- Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
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- 抗原
- UFD1L (Ubiquitin Fusion Degradation Protein 1 Homolog (UFD1L))
- 别名
- UFD1L (UFD1L 产品)
- 别名
- UFD1 antibody, Ufd1 antibody, ufd1 antibody, wu:fc55f04 antibody, zgc:92341 antibody, Ufd1l antibody, ubiquitin recognition factor in ER associated degradation 1 antibody, ubiquitin recognition factor in ER-associated degradation 1 antibody, ubiquitin fusion degradation 1 like (yeast) antibody, ubiquitin recognition factor in ER associated degradation 1 S homeolog antibody, ubiquitin fusion degradation protein 1 homolog antibody, Ubiquitin Fusion Degradation (yeast UFD homolog) antibody, UFD1 antibody, Ufd1 antibody, UFD1L antibody, ufd1.S antibody, ufd1l antibody, ufd1 antibody, EHI_125920 antibody, LOC100166745 antibody, LOC100635687 antibody, LOC100648660 antibody, ufd-1 antibody
- 背景
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Description: The protein encoded by this gene forms a complex with two other proteins, nuclear protein localization-4 and valosin-containing protein, and this complex is necessary for the degradation of ubiquitinated proteins. In addition, this complex controls the disassembly of the mitotic spindle and the formation of a closed nuclear envelope after mitosis. Mutations in this gene have been associated with Catch 22 syndrome as well as cardiac and craniofacial defects. Alternative splicing results in multiple transcript variants encoding different isoforms. A related pseudogene has been identified on chromosome 18.
Aliases: UFD1
- 分子量
- 34.5kDa
- 基因ID
- 7353
- HGNC
- 7353
- UniProt
- Q92890
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