HINT1 Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag)
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- 抗原 See all HINT1 蛋白
- HINT1 (Histidine Triad Nucleotide Binding Protein 1 (HINT1))
- 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 HINT1 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 HINT1 (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 HINT1 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
- HINT1 (Histidine Triad Nucleotide Binding Protein 1 (HINT1))
- 别名
- Hint1 (HINT1 产品)
- 别名
- hint Protein, pkci-1 Protein, prkcnh1 Protein, HINT Protein, NMAN Protein, PKCI-1 Protein, PRKCNH1 Protein, AA673479 Protein, Hint Protein, Ipk1 Protein, Pkci Protein, Prkci Protein, zgc:103764 Protein, CHPKCI Protein, HINTZ Protein, PKCIZ Protein, histidine triad nucleotide binding protein 1 Protein, histidine triad nucleotide binding protein 1 S homeolog Protein, histidine triad nucleotide binding protein 1-Z Protein, Histidine triad nucleotide-binding protein 1 Protein, HINT1 Protein, hint1 Protein, Hint1 Protein, hint1.S Protein, HINT1Z Protein, hint-1 Protein
- 背景
- This gene encodes a protein that hydrolyzes purine nucleotide phosphoramidates substrates, including AMP-morpholidate, AMP-N-alanine methyl ester, AMP-alpha-acetyl lysine methyl ester, and AMP-NH2. The encoded protein interacts with these substrates via a histidine triad motif. This gene is considered a tumor suppressor gene. In addition, mutations in this gene can cause autosomal recessive neuromyotonia and axonal neuropathy. There are several related pseudogenes on chromosome 7. Several transcript variants have been observed.
- 分子量
- 13.6 kDa
- NCBI登录号
- NP_005331
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