Anti-alpha smooth muscle Actin antibody (Ab5694)
ACTSA, ACTVS, GIG46, ACTA2, Alpha-actin-2, Cell growth-inhibiting gene 46 protein
详细信息
特异性
Alpha smooth muscle actin antibody (ab5694) stains smooth muscle cells in vessel walls, gut wall, and myometrium. Myoepithelial cells in breast and salivary gland are also stained. ab5694 reacts with tumors arising from smooth muscles and myoepithelial cells.
背景信息
Anti-alpha smooth muscle Actin antibody (ab5694) is a rabbit polyclonal antibody and is validated for use in IHC-P and WB. Anti-alpha smooth muscle Actin antibody (ab5694) was first used in a scientific publication in 1985 and has been cited over 3004 times in peer reviewed journals. It's performance in Western blot, immunofluorescence and IHC in human, mouse and rat samples is trusted by the scientific community. Abcam's high quality validation processes ensure Anti-alpha smooth muscle Actin antibody (ab5694) has high sensitivity and specificity. Anti-alpha smooth muscle Actin antibody (ab5694) has 150 independent reviews from customers. Anti-alpha smooth muscle Actin antibody (ab5694) specifically detects alpha smooth muscle Actin (UniProt ID: P62736; Molecular weight: 42kDa) and is sold in 100 µg selling sizes. Alpha-Smooth Muscle Actin (α-SMA) is a critical protein involved in smooth muscle contraction, encoded by the ACTA2 gene. Predominantly found in vascular smooth muscle cells, α-SMA plays a vital role in fibrogenesis and wound healing. It is often used as a marker for myofibroblast formation, which are specialized cells that contribute to tissue repair and fibrosis. The expression of α-SMA is associated with the activation of myofibroblasts, making it an important indicator in studies of fibrosis and other related conditions.
文献引用 (3325)
Fibroblasts of disparate developmental origins harbor anatomically variant scarring potential.
不同发育起源的成纤维细胞具有解剖学上不同的瘢痕形成潜能。
Pre-priming cell sheet therapy enabled by dynamic wrinkled electroactive substrate for muscle reconstruction.
利用动态皱纹电活性基质进行预激活细胞片疗法,实现肌肉重建。
High-entropy alloy Janus artificial enzymes for pH-gated sequential redox therapy of drug-resistant bacterial infection.
高熵合金 Janus 人工酶用于 pH 门控顺序氧化还原疗法治疗耐药细菌感染。
Mosaic partial epidermal reprogramming remodels neighbors and niches to refine skin homeostasis and repair.
表皮部分重塑嵌合体重塑邻近细胞和微环境,以改善皮肤稳态和修复。
Human iPSC-based Modeling of Pulmonary Fibrosis Reveals p300/CBP Inhibition Suppresses Alveolar Transitional Cell State.
基于人类 iPSC 的肺纤维化模型揭示 p300/CBP 抑制可抑制肺泡过渡细胞状态。
Macrophage-Derived Ferritin Exacerbates Silica-Induced Pulmonary Fibrosis via PIK3R2-Mediated Fibroblast Differentiation.
巨噬细胞衍生的铁蛋白通过 PIK3R2 介导的成纤维细胞分化加剧二氧化硅诱导的肺纤维化。
Single-Cell Mitochondrial Lineage Tracing Decodes Fate Decision and Spatial Clonal Architecture in Human Hematopoietic Organoids.
单细胞线粒体谱系追踪揭示人类造血类器官的命运决定和空间克隆结构。
Contribution of Gli1(+) Adventitial Stem Cells to Smooth Muscle Cells in Atherosclerosis and Vascular Injury.
Gli1(+)外膜干细胞对动脉粥样硬化和血管损伤中平滑肌细胞的贡献。
Mapping the Tissue-of-Origins of Mesenchymal Stromal Cells in Injury Repair.
损伤修复中间充质基质细胞的组织起源图谱。
Nanoparticle retention enables non-invasive detection of metastases by magnetic particle imaging in murine breast cancer models.
纳米颗粒滞留技术使得利用磁性颗粒成像技术在小鼠乳腺癌模型中实现对转移灶的非侵入性检测成为可能。
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