Anti-CD68 antibody [ED1] (Ab31630)
CD68 antigen, CD68 molecule, CD68_HUMAN, DKFZp686M18236, GP11, Gp110, LAMP4, MACROPHAGE ANTIGEN CD68, Macrophage antigen CD68 (microsialin), Macrosialin, SCARD1, Scavenger receptor class D member 1
详细信息
特异性
ab31630 recognises a single chain glycoprotein of 110kD that is expressed predominantly on the lysosomal membrane of myeloid cells. Weak cell surface expression also occurs. The antigen is expressed by the majority of tissue macrophages and weakly by peripheral blood granulocytes. Studies have shown that the antigen recognised by ED1 is the rat homologue of human CD68.
背景信息
Product Specifications Anti-CD68 antibody [ED1] (ab31630) is a mouse monoclonal antibody and is validated for use in Flow Cyt (Intra) in rat samples. Anti-CD68 antibody [ED1] (ab31630) specifically detects CD68 (UniProt ID: P34810; Molecular weight: 35kDa) and is sold in 125 µg selling sizes. Quality and Validation Abcam's high quality validation processes ensure Anti-CD68 antibody [ED1] (ab31630) has high sensitivity and specificity. Anti-CD68 antibody [ED1] (ab31630) has been cited over 403 times in peer reviewed journals and is trusted by the scientific community. Anti-CD68 antibody [ED1] (ab31630) has 20 independent reviews from customers. Target Information CD68 is a transmembrane glycoprotein predominantly expressed on macrophages, playing a crucial role in phagocytosis and antigen presentation. It is involved in various pathological conditions, including neuroinflammatory diseases, where it helps clear cellular debris and modulate immune response. CD68 expression is associated with several diseases, particularly those involving macrophage activity, including, cancer, neuroinflammation, Granular cell tumor and histiocytic sarcoma. This product should be stored undiluted.
文献引用 (392)
Chiral metal nanozyme-enabled SOD2 activation and siRNA delivery cooperatively mitigating chronic heart failure.
手性金属纳米酶激活 SOD2 和 siRNA 递送,协同缓解慢性心力衰竭。
Ameliorating post-infarction myocardial fibrosis and cardiac function via ROS-responsive hydrogel-mediated IL-11 antibody delivery.
通过 ROS 响应性水凝胶介导的 IL-11 抗体递送改善心肌梗死后心肌纤维化和心脏功能。
PROTAC-Mediated Degradation of mHTT Aggregates Attenuates Neurotoxicity in Cellular and R6/2 Mouse Models of Huntington's Disease.
PROTAC介导的mHTT聚集体降解可减轻亨廷顿病细胞和R6/2小鼠模型中的神经毒性。
Mesenchymal Stem Cell-Derived Apoptotic Micro-Vesicles Repaired Sciatic Nerve Defect by Regulating Early Inflammatory Microenvironment and Promoting Angiogenesis.
间充质干细胞衍生的凋亡微囊泡通过调节早期炎症微环境和促进血管生成修复坐骨神经缺陷。
S100A11 regulates microglial inflammatory response in neuropathic pain via H3K27ac-TFEB-mitochondrial autophagy axis.
S100A11 通过 H3K27ac-TFEB-线粒体自噬轴调节神经性疼痛中的小胶质细胞炎症反应。
Mechanotransduction-driven macrophage polarization via Integrin-SRC-STAT6 pathway in distraction osteogenesis.
机械转导驱动的巨噬细胞极化通过整合素-SRC-STAT6通路在牵引成骨中发挥作用。
Angiotensin-Converting Enzyme (ACE) Inhibitors and Statins Mitigate Negative Cardiovascular and Pulmonary Effects of Particulate Matter in a Mouse Exposure Model.
血管紧张素转换酶 (ACE) 抑制剂和他汀类药物可减轻颗粒物在小鼠暴露模型中对心血管和肺部的负面影响。
GCDCA promotes hepatocellular carcinoma progression through S1PR2/PI3K/AKT-mediated polarization of M2-type macrophages.
GCDCA 通过 S1PR2/PI3K/AKT 介导的 M2 型巨噬细胞极化促进肝细胞癌的进展。
Suppression of microglial activation with anti-inflammatory drug bindarit enhances neural development in the shunt-treated neonatal hydrocephalus model rat.
使用抗炎药物bindarit抑制小胶质细胞活化可增强分流治疗的新生儿脑积水模型大鼠的神经发育。
Notch-1 in macrophages promoted the ischemia-reperfusion via modulating EZH2/HSF1/BRD4/SIRPα/SHP2 induced ROS and apoptosis in cardiomyocyte.
巨噬细胞中的 Notch-1 通过调节 EZH2/HSF1/BRD4/SIRPα/SHP2 诱导的 ROS 和心肌细胞凋亡,促进缺血再灌注损伤。
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