- ￥900
- AAB
- 上海
- A18190
- 2025年10月29日
- WB,ELISA
- Rabbit
- Human,Mouse
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- 详细信息
- 技术资料
- 免疫原：
Synthesized peptide derived from human protein . at AA range: 170-250
- 形态：
Liquid in PBS containing 50% glycerol, and 0.02% sodium azide.
- 保存条件：
-20°C/1 year
- 克隆性：
Polyclonal
- 适应物种：
Human,Mouse
- 保质期：
1年
- 宿主：
Rabbit
- 应用范围：
WB,ELISA
- 浓度：
1 mg/ml
- 靶点：
NDUFV1 UQOR1
- 抗体英文名：
NDUV1 rabbit pAb
- 抗体名：
NADH dehydrogenase [ubiquinone] flavoprotein 1, mitochondrial (EC 1.6.5.3) (EC 1.6.99.3) (Complex I-51kD) (CI-51kD) (NADH dehydrogenase flavoprotein 1) (NADH-ubiquinone oxidoreductase 51 kDa subunit)
- 规格：
50ul
NADH:ubiquinone oxidoreductase core subunit V1(NDUFV1) Homo sapiens The mitochondrial respiratory chain provides energy to cells via oxidative phosphorylation and consists of four membrane-bound electron-transporting protein complexes (I-IV) and an ATP synthase (complex V). This gene encodes a 51 kDa subunit of the NADH:ubiquinone oxidoreductase complex I; a large complex with at least 45 nuclear and mitochondrial encoded subunits that liberates electrons from NADH and channels them to ubiquinone. This subunit carries the NADH-binding site as well as flavin mononucleotide (FMN)- and Fe-S-biding sites. Defects in complex I are a common cause of mitochondrial dysfunction; a syndrome that occurs in approximately 1 in 10,000 live births. Mitochondrial complex I deficiency is linked to myopathies, encephalomyopathies, and neurodegenerative disorders such as Parkinson's disease and Leigh syndrome. Alternative splicing results in multiple trans
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NDUV1 rabbit pAb
￥900
