BML 283,Ca 2+螯合剂

BAPTA-AM (订货以英文为准)

编号:B115502
CAS号:126150-97-8
分子式:C34H40N2O18
分子量:764.68
货号 品牌 包装 目录价 您的价格 库存 数量 购买
B115502-100mg 阿拉丁 100mg ¥1059.90
B115502-25mg 阿拉丁 25mg ¥370.90
产品名称 BAPTA-AM
中文名称 BML 283,Ca 2+螯合剂
CAS号 126150-97-8
分子式(M.F.) C34H40N2O18
分子量(M.W.) 764.68
储存条件 -20°C储存
熔点98 °C
敏感性对热敏感
溶解性DMSO: 20 mg/mL;insoluble in water & Ethanol
存贮条件储存温度:-20°C
密度1.3500
应用A membrane-permeable form of BAPTA;Selective chelator of intracellular Ca2+ stores.· 降低剪切后半胱氨酸蛋白酶-3升高水平· 阻止细胞死亡,抑制ROS(活性氧化簇)产物,抑制半胱氨酸蛋白酶-8活性。· 排除细胞内Ca2+ ([Ca2+]i) 浓度变化对癫痫诱导影响· 消除6-羟多巴胺(6-OHDA)诱导的[Ca2+]i增量水平
产品介绍BAPTA/AM [1,2-Bis(2-aminophenoxy)ethane-N,N,N′,N′-tetraacetic acid tetrakis(acetoxymethyl ester)] is a non-fluorescent, membrane-permeable form of BAPTA. Whereas the BAPTA, Free acid is not cell permeable and is only useful for manipulating extracellular Ca2+ levels, BAPTA/AM can be used with a wide variety of cells, where it is hydrolyzed by cytosolic esterases and trapped intracellularly. Experiments have shown that BAPTA/AM abolishes vitamin D3-induced increase in intracellular Ca2+, and may induce inactivation of protein kinase C. Has also been shown to inhibit thapsigargin-induced apoptosis in rat thymocytes. This product is a high quality and sensitive compound for calcium signaling studies, investigation of signal transduction and apoptotic cascades, and neuroscience research. BAPTA-AM抑制自由基介导的毒性,增强非神经细胞中细胞凋亡,保护神经细胞免受缺血性损伤。它调节离子通道,阻止神经Ca2+-激活K+通道电流。BAPTA-AM维持细胞内Ca2+动态平衡。
生化机理细胞内Ca2+储存选择性螯合剂。
别名1,2-双(2-氨基苯氧基)乙烷-N,N,N`,N`-四乙酸四乙酸甲酯;胞内钙荧光探针BAPTA-AM;1,2-双(2-氨基苯氧基)乙烷-N,N,N',N'-四乙酸四(乙酸基甲基)酯;1,2-双(2-氨基苯氧基)-乙烷-N,N,N,N′-四乙酸;1,2-Bis(2-aminophenoxy)ethane-N,N,N′,N′-tetraacetic acid tetrakis(acetoxymethyl ester);Tetrakis(acetoxymethyl) 1,2-Bis(2-aminophenoxy)ethane-N,N,N',N'-tetraacetate;1,2-Bis(2-aminophenoxy)ethane-N,N,N',N'-tetraacetic Acid Tetrakis(acetoxymethyl) Ester
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