Methylmalonic Aciduria (Cobalamin Deficiency) Type A (MMAA) (N-Term) Peptide
MMAA
适用: 人
宿主: 合成
BP, WB
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- 抗原 See all MMAA products
- MMAA (Methylmalonic Aciduria (Cobalamin Deficiency) Type A (MMAA))
- 蛋白结构域
- N-Term
- 宿主
- 人
- 资源
- 合成
- 应用范围
- Blocking Peptide (BP), Western Blotting (WB)
- 序列
- GQRACLAEAI TLVESTHSRK KELAQVLLQK VLLYHREQEQ SNKGKPLAFR
- 产品特性
- This is a synthetic peptide designed for use in combination with anti-MMAA 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
- MMAA (Methylmalonic Aciduria (Cobalamin Deficiency) Type A (MMAA))
- 别名
- 2810018E08Rik Peptide, AI840684 Peptide, cblA Peptide, methylmalonic aciduria (cobalamin deficiency) type A Peptide, methylmalonic aciduria (cobalamin deficiency) cblA type Peptide, Mmaa Peptide, MMAA Peptide
- 背景
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The protein encoded by this gene is involved in the translocation of cobalamin into the mitochondrion, where it is used in the final steps of adenosylcobalamin synthesis. Adenosylcobalamin is a coenzyme required for the activity of methylmalonyl-CoA mutase. Defects in this gene are a cause of methylmalonic aciduria.
Alias Symbols: MGC120010, MGC120011, MGC120012, MGC120013, cblA
Protein Interaction Partner: MUT
Protein Size: 418 - 分子量
- 46 kDa
- 基因ID
- 166785
- NCBI登录号
- NM_172250, NP_758454
- UniProt
- Q8IVH4
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