Anti-beta Actin antibody - Loading Control (Ab8227)
Beta-actin, ACTB
用户验证的应用
推荐稀释比例
- IHC-P0.2-1 µg/mL We recommend Goat Anti-Rabbit IgG H&L (Biotin) ( ab6720 ) secondary antibody or Goat Anti-Rabbit IgG Fc (HRP) ( ab97200 ) secondary antibody. Perform heat-mediated antigen retrieval before commencing with IHC staining protocol.
- WB1/1000 - 1/5000 We recommend Goat Anti-Rabbit IgG H&L (HRP) ( ab6721 ) secondary antibody. A stronger signal is observed in chemiluminescent western blot when using 2% BSA as the blocking agent. Milk blocking is suitable for use with fluorescent detection systems.
- ICC/IF1 µg/mL
详细信息
背景信息
Anti-beta Actin antibody (ab8227) is a rabbit polyclonal antibody and is validated for use in ICC/IF, IHC-P and WB. Anti-beta Actin antibody (ab8227) was first used in a scientific publication in 1991 and has been cited over 4031 times in peer reviewed journals. It's performance in Western blot in human, mouse and rat samples is trusted by the scientific community. Abcam's high quality validation processes ensure Anti-beta Actin antibody (ab8227) has high sensitivity and specificity. Anti-beta Actin antibody (ab8227) has 104 independent reviews from customers. beta Actin antibodies are often used as loading controls in Western Blot. Anti-beta Actin antibody has been verified in Western Blot samples and detects a band at 42kDa Molecular weight. Anti-beta Actin antibody (ab8227) specifically detects beta Actin (UniProt ID: P60709; Molecular weight: 42kDa) and is sold in 50 µg selling sizes. Beta-Actin (β-actin) is a highly conserved protein that plays a crucial role in cell motility, structure and integrity. It is one of the six actin isoforms found in humans and is a major component of the cytoskeleton in non-muscle cells. β-actin is involved in various cellular processes, including cell division, signaling and maintaining cell shape. Due to its ubiquitous expression and stability, β-actin is commonly used as a loading control in western blotting (WB) and other protein quantification assays. Understanding β-actin's functions and interactions is essential for studying cellular dynamics and various physiological processes.
文献引用 (4531)
SIRT2-mediated deacetylation of LCK governs the magnitude of T cell receptor signaling.
SIRT2 介导的 LCK 去乙酰化控制着 T 细胞受体信号的强度。
2'-O-Methyl-guanosine RNA fragments antagonize TLR7 and TLR8 to limit autoimmunity.
2'-O-甲基鸟苷RNA片段拮抗TLR7和TLR8,从而限制自身免疫。
Monovalent pseudo-natural products supercharge degradation of IDO1 by its native E3 KLHDC3.
单价伪天然产物可加速 IDO1 的天然 E3 KLHDC3 的降解。
Tumour acidosis remodels the glycocalyx to control lipid scavenging and ferroptosis.
肿瘤酸中毒重塑糖萼,以控制脂质清除和铁死亡。
ER-tethering directs TREX1 penetration of a BAF-dependent barrier at micronuclei.
内质网锚定引导 TREX1 穿透微核处 BAF 依赖性屏障。
Covalent modification of a glutamic acid inspired by HaloTag technology.
受 HaloTag 技术启发,对谷氨酸进行共价修饰。
Single-cell thiol profiling enabled by live-cell labeling reveals metabolic heterogeneity in ferroptosis.
利用活细胞标记技术进行单细胞硫醇分析,揭示了铁死亡过程中的代谢异质性。
NAA40 and NAC cooperate in co-translational histone acetylation in humans.
NAA40 和 NAC 在人类的共翻译组蛋白乙酰化过程中协同作用。
Combined targeted and epigenetic-based therapy enhances antitumor immunity by stabilizing GATA6-dependent MHCI expression in pancreatic ductal adenocarcinoma.
靶向治疗与表观遗传治疗相结合,通过稳定胰腺导管腺癌中 GATA6 依赖的 MHCI 表达来增强抗肿瘤免疫力。
Loss of Fsr quorum sensing promotes biofilm formation and worsens outcomes in enterococcal infective endocarditis.
Fsr 群体感应的丧失会促进生物膜的形成,并使肠球菌感染性心内膜炎的预后恶化。
- 1
- 2
- 3
- 4
- 5
- 6
- 454