Solute Carrier Family 19 (Thiamine Transporter), Member 2 (SLC19A2) (C-Term) Peptide
SLC19A2
适用: 人
宿主: 合成
BP, WB
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- 抗原 See all SLC19A2 products
- SLC19A2 (Solute Carrier Family 19 (Thiamine Transporter), Member 2 (SLC19A2))
- 蛋白结构域
- C-Term
- 宿主
- 人
- 资源
- 合成
- 应用范围
- Blocking Peptide (BP), Western Blotting (WB)
- 序列
- LGLEITTQFL IYASYFALIA VVFLASGAVS VMKKCRKLED PQSSSQVTTS
- 产品特性
- This is a synthetic peptide designed for use in combination with anti-SLC19A2 Antibody. It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
- 纯化方法
- Purified
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- 应用备注
- Each Investigator should determine their own optimal working dilution for specific applications.
- 限制
- 仅限研究用
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- 状态
- Lyophilized
- 溶解方式
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
- 浓度
- 1 mg/mL
- 缓冲液
- Final peptide concentration is 1 mg/mL in PBS.
- 注意事项
- Avoid repeated freeze-thaw cycles.
- 储存条件
- -20 °C
- 储存方法
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- 抗原
- SLC19A2 (Solute Carrier Family 19 (Thiamine Transporter), Member 2 (SLC19A2))
- 别名
- SLC19A2 Peptide, TC1 Peptide, THMD1 Peptide, THT1 Peptide, THTR1 Peptide, TRMA Peptide, solute carrier family 19 member 2 Peptide, solute carrier family 19 (thiamine transporter), member 2 Peptide, Slc19a2 Peptide, SLC19A2 Peptide, slc19a2 Peptide
- 背景
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This gene encodes the thiamin transporter protein. Mutations in this gene cause thiamin-responsive megaloblastic anemia syndrome (TRMA), which is an autosomal recessive disorder characterized by diabetes mellitus, megaloblastic anemia and sensorineural deafness.
Alias Symbols: TC1, THT1, THTR1, TRMA, THMD1
Protein Size: 497 - 分子量
- 55 kDa
- 基因ID
- 10560
- NCBI登录号
- NM_006996, NP_008927
- UniProt
- O60779
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