Anti-COX IV antibody [20E8C12] - Mitochondrial Marker (Ab14744)
COX4, COX4I1, Cytochrome c oxidase polypeptide IV, Cytochrome c oxidase subunit IV isoform 1, COX IV-1
详细信息
背景信息
What is this antibody validated in? Anti-COX IV antibody [20E8C12] (ab14744) is a mouse monoclonal antibody and is validated for use in Western Blot (WB), Flow Cytometry (Flow Cyt) in Cow, Human, Mouse, Rat samples. Trusted by the scientific community Anti-COX IV [20E8C12] (ab14744) was first used in a scientific publication in 2004 and has been cited over 330 times in peer-reviewed journals. Reviewed by scientists Anti-COX IV [20E8C12] (ab14744) has over 20 independent reviews from customers. Want a custom formulation? This antibody clone is manufactured by Abcam. If you require a custom buffer formulation or conjugation for your experiments, please contact orders@abcam.com
文献引用 (236)
Engineering mtDNA deletions by reconstituting end joining in human mitochondria
通过在人类线粒体中重建末端连接来构建线粒体DNA缺失
TANGO2 binds crystallin alpha B and its loss causes desminopathy.
TANGO2 与晶状体蛋白 α B 结合，其缺失会导致结蛋白病
Mitochondrial translation regulates terminal erythroid differentiation by maintaining iron homeostasis
线粒体翻译通过维持铁稳态来调节终末红细胞分化
C3aR1 on β cells enhances β cell function and survival to maintain glucose homeostasis.
β细胞上的C3aR1增强β细胞功能和存活，以维持葡萄糖稳态
Mitochondrial dysfunction, iron accumulation, lipid peroxidation, and inflammasome activation in cellular models derived from patients with multiple sclerosis.
多发性硬化症患者细胞模型中线粒体功能障碍、铁积累、脂质过氧化和炎症小体激活
COA5 has an essential role in the early stage of mitochondrial complex IV assembly
COA5 在线粒体复合物IV组装的早期阶段起着至关重要的作用
Acupuncture alleviates hemorrhagic transformation after delayed rt-PA treatment for acute ischemic stroke by regulating the mitophagy-NLRP3 inflammasome pathway.
针灸通过调节线粒体自噬-NLRP3炎症小体通路，减轻急性缺血性中风延迟rt-PA治疗后的出血性转化
GL261 glioblastoma induces delayed body weight gain and stunted skeletal muscle growth in young mice.
GL261 胶质母细胞瘤可导致幼鼠体重增长延迟和骨骼肌生长发育迟缓
Biotin Induces Inactive Chromosome X Reactivation and Corrects Physiopathological Alterations in Beta-Propeller-Protein-Associated Neurodegeneration
生物素诱导失活的X染色体重新激活，并纠正β-螺旋桨蛋白相关神经退行性疾病的病理生理改变。
Adult Leigh Syndrome Associated with the m.15635T>C Mitochondrial DNA Variant Affecting the Cytochrome b (MT-CYB) Gene
与影响细胞色素 b (MT-CYB) 基因的 m.15635T>C 线粒体 DNA 变异相关的成人 Leigh 综合征
- 1
- 2
- 3
- 4
- 5
- 6
- 24