ATPase, Ca++ Transporting, Type 2C, Member 1 (ATP2C1) Peptide
ATP2C1
适用: 人
宿主: 合成
BP, WB
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- 抗原 See all ATP2C1 products
- ATP2C1 (ATPase, Ca++ Transporting, Type 2C, Member 1 (ATP2C1))
- 宿主
- 人
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资源
- 合成
- 应用范围
- Blocking Peptide (BP), Western Blotting (WB)
- 产品特性
- This is a synthetic peptide designed for use in combination with anti-ATP2C1 antibody (Catalog #: ARP44399_P050). 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
- ATP2C1 (ATPase, Ca++ Transporting, Type 2C, Member 1 (ATP2C1))
- 别名
- ATP2C1 Peptide, ATP2C1A Peptide, BCPM Peptide, HHD Peptide, PMR1 Peptide, SPCA1 Peptide, hSPCA1 Peptide, Spca1 Peptide, si:dkey-11p23.6 Peptide, SPCA Peptide, 1700121J11Rik Peptide, AW061228 Peptide, D930003G21Rik Peptide, pmr1 Peptide, ATPase secretory pathway Ca2+ transporting 1 Peptide, ATPase, Ca++ transporting, type 2C, member 1 Peptide, ATPase, Ca++-sequestering Peptide, ATP2C1 Peptide, atp2c1 Peptide, Atp2c1 Peptide
- 背景
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ATP2C1 belongs to the family of P-type cation transport ATPases. This magnesium-dependent enzyme catalyzes the hydrolysis of ATP coupled with the transport of the calcium. Defects in this gene cause Hailey-Hailey disease, an autosomal dominant disorder. Alternatively spliced transcript variants encoding different isoforms have been identified.The protein encoded by this gene belongs to the family of P-type cation transport ATPases. This magnesium-dependent enzyme catalyzes the hydrolysis of ATP coupled with the transport of the calcium. Defects in this gene cause Hailey-Hailey disease, an autosomal dominant disorder. Alternatively spliced transcript variants encoding different isoforms have been identified.
Alias Symbols: ATP2C1A, BCPM, HHD, KIAA1347, PMR1, SPCA1, hSPCA1
Protein Size: 888 - 分子量
- 98 kDa
- 基因ID
- 27032
- NCBI登录号
- NM_001001485, NP_001001485
- UniProt
- P98194
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