UFD1L Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag)
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- 抗原 See all UFD1L 蛋白
- UFD1L (Ubiquitin Fusion Degradation Protein 1 Homolog (UFD1L))
- 蛋白类型
- Recombinant
- 产品特性
- Transcript Variant 1
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宿主
- 人
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资源
- HEK-293 Cells
- 标记
- This UFD1L protein is labelled with Myc-DYKDDDDK Tag.
- 应用范围
- Antibody Production (AbP), Standard (STD)
- 产品特性
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- Recombinant human UFD1L (transcript variant 1) protein expressed in HEK293 cells.
- Produced with end-sequenced ORF clone
- 纯度
- > 80 % as determined by SDS-PAGE and Coomassie blue staining
- Top Product
- Discover our top product UFD1L 蛋白
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- 应用备注
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Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays - 说明
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The tag is located at the C-terminal.
- 限制
- 仅限研究用
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- 浓度
- 50 μg/mL
- 缓冲液
- 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
- 储存条件
- -80 °C
- 储存方法
- Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
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- 抗原
- UFD1L (Ubiquitin Fusion Degradation Protein 1 Homolog (UFD1L))
- 别名
- Ufd1l (UFD1L 产品)
- 别名
- UFD1 Protein, Ufd1 Protein, ufd1 Protein, wu:fc55f04 Protein, zgc:92341 Protein, Ufd1l Protein, ubiquitin recognition factor in ER associated degradation 1 Protein, ubiquitin recognition factor in ER-associated degradation 1 Protein, ubiquitin fusion degradation 1 like (yeast) Protein, ubiquitin recognition factor in ER associated degradation 1 S homeolog Protein, ubiquitin fusion degradation protein 1 homolog Protein, Ubiquitin Fusion Degradation (yeast UFD homolog) Protein, UFD1 Protein, Ufd1 Protein, UFD1L Protein, ufd1.S Protein, ufd1l Protein, ufd1 Protein, EHI_125920 Protein, LOC100166745 Protein, LOC100635687 Protein, LOC100648660 Protein, ufd-1 Protein
- 背景
- 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.
- 分子量
- 34.3 kDa
- NCBI登录号
- NP_005650
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