Anti-Actin antibody [EPR16769] - Loading Control (Ab179467)
ACTA, ACTA1, Alpha-actin-1
详细信息
背景信息
What is this antibody validated in? Anti-Actin antibody [EPR16769] (ab179467) is a rabbit recombinant monoclonal antibody and is validated for use in Western Blot (WB), Flow Cytometry (Intra), Flow Cytometry (Flow Cyt), Immunoprecipitation (IP), Immunohistochemistry (IHC-P), Immunocytochemistry/immunofluorescence (ICC/IF) in Chicken, Human, Mouse, Rat samples. What is the molecular weight of Actin? Anti-Actin [EPR16769] (ab179467) specifically detects a band for Actin (UniProt: P68133) at a molecular weight of 42kDa. Trusted by the scientific community Anti-Actin [EPR16769] (ab179467) was first used in a scientific publication in 2014 and has been cited over 420 times in peer-reviewed journals. Reviewed by scientists Anti-Actin [EPR16769] (ab179467) has over 10 independent reviews from customers. Trial sizes available! Test your antibody or perform pre-screening before committing to a larger quantity. Sold in 20µl. Discover our selection of trial-size antibodies. Patented technology Our RabMAb ® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb ® patents. What are the advantages of a recombinant monoclonal antibody? This product is a recombinant monoclonal antibody, which offers several advantages including - High batch-to-batch consistency and reproducibility - Improved sensitivity and specificity - Long-term security of supply - Animal-free batch production For more information, read more on recombinant antibodies.
文献引用 (540)
Mutations in mitochondrial ferredoxin FDX2 suppress frataxin deficiency.
线粒体铁氧还蛋白 FDX2 的突变可抑制弗拉塔辛缺乏症。
Unraveling the Morphological and Functional Maturation Mechanisms Underlying Human Neural Development Using iPSCs-Derived Neuronal Model.
利用iPSCs衍生的神经元模型揭示人类神经发育的形态和功能成熟机制。
Functional characterization of SDHB variants clarifies hereditary pheochromocytoma and paraganglioma risk and genotype-phenotype relationships.
SDHB 变异体的功能表征阐明了遗传性嗜铬细胞瘤和副神经节瘤的风险以及基因型-表型关系。
Targeted AAV6 gene therapy restores corneal endothelial function in three hereditary corneal dystrophies.
靶向 AAV6 基因疗法可恢复三种遗传性角膜营养不良症患者的角膜内皮功能。
Intelligent nanoliposome ameliorate chronic intermittent hypoxia-mediated neuronal injury via a dual regulation microglial inflammation strategy.
智能纳米脂质体通过双重调节小胶质细胞炎症策略改善慢性间歇性缺氧介导的神经元损伤。
APOA2-mediated endothelial mesenchymal transition and cancer lipid metabolism reprogramming confers antiangiogenic drug resistance through TGF-β.
APOA2 介导的内皮间质转化和癌症脂质代谢重编程通过 TGF-β 赋予抗血管生成药物耐药性。
Antioxidant and Anti-Aging Effects of Porphyra-334 Produced from Saccharomyces cerevisiae in Human Skin Models.
利用酿酒酵母产生的紫菜-334在人体皮肤模型中表现出抗氧化和抗衰老作用。
Serum Amyloid A-Dependent Inflammasome Activation and Acute Injury in a Mouse Model of Experimental Stroke.
血清淀粉样蛋白 A 依赖性炎症小体激活与小鼠实验性中风模型中的急性损伤。
TRIC-A Loss Sensitizes the Heart to β-Adrenergic Stress and Drives Cardiomyocyte Death and Fibrosis.
TRIC-A 的缺失使心脏对 β-肾上腺素能应激更加敏感,并导致心肌细胞死亡和纤维化。
NSUN2 restrains gastric cancer cell apoptosis and ferroptosis by promoting the m5C modification of EPYC.
NSUN2 通过促进 EPYC 的 m5C 修饰来抑制胃癌细胞凋亡和铁死亡。
- 1
- 2
- 3
- 4
- 5
- 6
- 54