NADH Dehydrogenase (Ubiquinone) 1 alpha Subcomplex, Assembly Factor 2 (NDUFAF2) (N-Term) Peptide
NDUFAF2
适用: 人
宿主: 合成
BP, WB
-
- 抗原 See all NDUFAF2 products
- NDUFAF2 (NADH Dehydrogenase (Ubiquinone) 1 alpha Subcomplex, Assembly Factor 2 (NDUFAF2))
- 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
- HVGTDQFGNK YYYIPQYKNW RGQTIREKRI VEAANKKEVD YEAGDIPTEW
- 产品特性
- This is a synthetic peptide designed for use in combination with anti-NDUFAF2 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
-
-
- 应用备注
- Each Investigator should determine their own optimal working dilution for specific applications.
- 限制
- 仅限研究用
-
- 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.
-
- 抗原
- NDUFAF2 (NADH Dehydrogenase (Ubiquinone) 1 alpha Subcomplex, Assembly Factor 2 (NDUFAF2))
- 别名
- B17.2L Peptide, MMTN Peptide, NDUFA12L Peptide, mimitin Peptide, Ndufa12l Peptide, RGD1560158 Peptide, NDUFAF2 Peptide, ndufa12l Peptide, zgc:101036 Peptide, 1810058I14Rik Peptide, C86051 Peptide, NADH:ubiquinone oxidoreductase complex assembly factor 2 Peptide, NADH:ubiquinone oxidoreductase complex assembly factor 2 L homeolog Peptide, NADH dehydrogenase (ubiquinone) complex I, assembly factor 2 Peptide, NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, assembly factor 2 Peptide, NDUFAF2 Peptide, Ndufaf2 Peptide, ndufaf2.L Peptide, ndufaf2 Peptide
- 背景
-
NADH:ubiquinone oxidoreductase (complex I) catalyzes the transfer of electrons from NADH to ubiquinone (coenzyme Q) in the first step of the mitochondrial respiratory chain, resulting in the translocation of protons across the inner mitochondrial membrane. This gene encodes a complex I assembly factor. Mutations in this gene cause progressive encephalopathy resulting from mitochondrial complex I deficiency.
Alias Symbols: B17.2L, FLJ22398, MMTN, NDUFA12L, mimitin
Protein Size: 169 - 分子量
- 20 kDa
- 基因ID
- 91942
- NCBI登录号
- NM_174889, NP_777549
- UniProt
- Q8N183
-
You are here:
