Anti-Human/Mouse NDUFA12 Polyclonal Antibody

NDUFA12多克隆抗体

This gene encodes a protein which is part of mitochondrial complex 1, part of the oxidative phosphorylation system in mitochondria. Complex 1 transfers electrons to ubiquinone from NADH which establishes a proton gradient for the generation of ATP. Mutations in this gene are associated with Leigh syndrome due to mitochondrial complex 1 deficiency. Pseudogenes of this gene are located on chromosomes 5 and 13. Alternative splicing results in multiple transcript variants.
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基本信息

数据文档 查看数据文档
货号 PA11361
规格 100μl
宿主 Rabbit
免疫原 Synthetic peptide of human NDUFA12
特异性
亚型 IgG
反应性 Human,Mouse
克隆
Uniprot Q9UI09
浓度 0.4 mg/mL
推荐稀释度 IHC 1:50-1:200
配方
应用范围 IHC,ELISA
别名 13 kDa differentiation associated protein,13 kDa differentiation-associated protein,2410011G03Rik,AW112974,B17.2,CI-B17.2,CIB17.2,Complex I B17.2,Complex I B17.2 subunit,Complex I-B17.2,DAP13,MGC107642,MGC7999,NADH dehydrogenase (ubiquinone) 1 alpha subcomplex 12,NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 12,NADH ubiquinone oxidoreductase subunit B17.2,NADH-ubiquinone oxidoreductase subunit B17.2,NDUAC,NDUFA12,RGD1311462
保存条件 冻干产品: 2 - 8°C保存5年; 液体: -20°C保存2年.
注意 仅用于科学研究, 不能用于疾病诊断.

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