PI-9 is a potent inhibitor of granzyme B and of granzyme B-mediated apoptosis,and is also an inhibitor of capase-1 and,to a smaller extent,caspase-4 and caspase-8. PI-9 expression is also upregulated in response to inflammatory stimuli. This upregulation protects cells from apoptosis ...
所在地:中国大陆 产品型号:Anti-caspase-9 p10 简单介绍:半胱胺酸蛋白酶蛋白9-p10抗体现货供应。可用于ELISA,免疫组化,免疫荧光,WB等试验,半胱胺酸蛋白酶蛋白9-p10抗体是满足不同应用的高效抗体。公司创新的将客户抗体的*终应用需求放在位,从源头开始为客户系统性的制定*优化解决方案。 在线询价相关...
INHIBITOROFCASPASE-ACTIVATEDDNASE(ICAD),N-TERMINAL,RABBITANTI-MOUSE:WB 中文名: 中文别名: CBNumber: CB11220905 分子式: 分子量: 0 MOL File: Mol file 化学性质安全信息用途供应商1 INHIBITOROFCASPASE-ACTIVATEDDNASE(ICAD),N-TERMINAL,RABBITANTI-MOUSE:WB化学性质 ...
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Exemplary compounds useful in the methods of the invention are provided herein.Lawrence FritzKevin TomaselliDonald KaranewskySteven LintonXu BaiUSUS20040058850 * Sep 2, 2003 Mar 25, 2004 Idun Pharmaceuticals, Inc. Using caspase inhibitor; antiinflammatory agents...
Anti-ICAD(Inhibitor of Caspase-Activated Dnase )??Caspase 激活的脱氧核糖核酸酶抑制剂 价格电议 起批量≥1 盒 最小起订1盒 供货总量136盒 发货地址上海市奉贤区 建议售价￥电议 更新日期2025年02月10日 即时洽谈立即询价查看联系方式 收藏产品发送留言 ...
上海玉博生物科技有限公司 主要致力于“Anti-ICAD/DFF-40β(Inhibitor of Caspase-Activated Dnase ) Caspase 激活的脱氧核糖核酸酶抑制剂 yb-0214R”的生产销售。多年的“Anti-ICAD/DFF-40β(Inhibitor of Caspase-Activated Dnase ) Caspase 激活的脱氧核糖核酸酶
BY-K0050R Anti-Caspase-9??白介素1-β转化酶样凋亡蛋白酶6抗体 BY-K0803R Anti-BRCA1(Breast cancer susceptbility gene 1)(human)??易感基因1抗体(人) BY-K1122R Anti-Sema3F (semaphorin 3F)??臂板蛋白3F抗体 BY-K0742R Anti-P27/kip1 (cyclin-dependent kinase inhibitor 1B)??P27抗体/周期...
Cell pellets were lysed using urea lysis buffer containing 9 M urea, 50 mM Tris-HCl (pH 8.0), 150 mM NaCl, 1 mM EDTA, and protease inhibitor (Roche). Lysates were centrifuged to remove cell debris and lysates with an equal amount of proteins from two samples were mixed, reduce...
Where cytochrome c binds Apaf-1 and activate procaspase-9, forming an apoptosome and leads to activation of caspase-9 [23]. On the basis of the above assumptions and in a continuation to our research directed towards the synthesis of bioactive heterocycles [24–28], herein our studies focus...