Valyl-tRNA Synthetase 2, Mitochondrial (VARS2) protein (Myc-DYKDDDDK Tag)
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- 抗原 See all Valyl-tRNA Synthetase 2, Mitochondrial (VARS2) 蛋白
- Valyl-tRNA Synthetase 2, Mitochondrial (VARS2)
- 蛋白类型
- Recombinant
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宿主
- 人
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资源
- HEK-293 Cells
- 标记
- Myc-DYKDDDDK Tag
- 应用范围
- Antibody Production (AbP), Standard (STD)
- 产品特性
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- Recombinant human Valyl-tRNA synthetase 2, mitochondrial (putative) (VARS2), nuclear gene encoding mitochondrial protein 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 VARS2 蛋白
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Valyl-tRNA Synthetase 2, Mitochondrial (VARS2) (AA 27-1063) protein (His tag)
Crystallography grade VARS2 宿主: 人 宿主: Insect Cells Recombinant >95 % as determined by SDS PAGE, Size Exclusion Chromatography and Western Blot. SDS, WB, Crys, ELISA
Valyl-tRNA Synthetase 2, Mitochondrial (VARS2) (AA 16-1060) protein (His tag)Crystallography grade VARS2 宿主: 小鼠 宿主: Insect Cells Recombinant >95 % as determined by SDS PAGE, Size Exclusion Chromatography and Western Blot. SDS, WB, Crys, ELISA
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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
- Valyl-tRNA Synthetase 2, Mitochondrial (VARS2)
- 别名
- Valyl-Trna Synthetase 2, Mitochondrial (Putative) (Vars2) (VARS2 产品)
- 别名
- VARS2 Protein, G7a Protein, VARS2L Protein, VARSL Protein, Vars2l Protein, Varsl Protein, 1190004I24Rik Protein, mKIAA1885 Protein, valyl-tRNA synthetase 2, mitochondrial Protein, VARS2 Protein, Vars2 Protein
- 背景
- This gene encodes a mitochondrial aminoacyl-tRNA synthetase, which catalyzes the attachment of valine to tRNA(Val) for mitochondrial translation. Mutations in this gene cause combined oxidative phosphorylation deficiency-20, and are also associated with early-onset mitochondrial encephalopathies. Alternative splicing of this gene results in multiple transcript variants.
- 分子量
- 118.3 kDa
- NCBI登录号
- NP_065175
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