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- 小鼠 单克隆 (84H10)
反应物种: 人类, 狗
应用: 酶联免疫吸附测定, 免疫沉淀, 流式细胞仪
文章摘录数: 3
Published customer image: . ICAM-1 activates PKC but not PKC II in HMVECLs. A ) At 70% confluence, HMVECLs cells pretreated with 10 ng/ml TNF to induce ICAM-1 expression. At 24 hrs, the cells were suspended and immunolabeled with anti-ICAM-1 antibodies and examined by flow cytometry for ICAM-1 expression. B–D) HMVECLs were pretreated with TNF as in panel A. At 24 hrs, the endothelial cells were nonstimulated (NS) or stimulated with a confluent monolayer of anti-ICAM-1-coated beads or the control anti-PECAM-1-coated beads for 20 minutes in B and D or for the times indicated in C. The cells were lysed and the activation of PKC II and PKC was examined by western blot with B) anti-phospho-PKC IIThr641 or anti-PKC II or C–D) anti-phospho- PKC Thr638 or anti-PKC . Shown are representative blots. Shown are the mean SEM of 3 experiments. NT, nontreated. *, p 0.05 as compared to the nontreated (NT) groups. From: Abdala-Valencia H, Berdnikovs S, Cook-Mills JM (2012). Vitamin E Isoforms Differentially Regulate Intercellular Adhesion Molecule-1 Activation of PKC in Human Microvascular Endothelial Cells. PLoS ONE 7(7): e41054 .
规格: 0.2毫克
价格: 325美元
至产商 - 小鼠 单克隆 (84H10)
反应物种: 人类, 狗
共轭标签: 异硫氰酸荧光素
应用: 流式细胞仪
文章摘录数: 1
Published customer image: . ICAM-1 activates PKC but not PKC II in HMVECLs. A ) At 70% confluence, HMVECLs cells pretreated with 10 ng/ml TNF to induce ICAM-1 expression. At 24 hrs, the cells were suspended and immunolabeled with anti-ICAM-1 antibodies and examined by flow cytometry for ICAM-1 expression. B–D) HMVECLs were pretreated with TNF as in panel A. At 24 hrs, the endothelial cells were nonstimulated (NS) or stimulated with a confluent monolayer of anti-ICAM-1-coated beads or the control anti-PECAM-1-coated beads for 20 minutes in B and D or for the times indicated in C. The cells were lysed and the activation of PKC II and PKC was examined by western blot with B) anti-phospho-PKC IIThr641 or anti-PKC II or C–D) anti-phospho- PKC Thr638 or anti-PKC . Shown are representative blots. Shown are the mean SEM of 3 experiments. NT, nontreated. *, p 0.05 as compared to the nontreated (NT) groups. From: Abdala-Valencia H, Berdnikovs S, Cook-Mills JM (2012). Vitamin E Isoforms Differentially Regulate Intercellular Adhesion Molecule-1 Activation of PKC in Human Microvascular Endothelial Cells. PLoS ONE 7(7): e41054 .
规格: 100 TESTS
价格: 273美元
至产商 - 小鼠 单克隆 (84H10)
反应物种: 人类, 狗
应用: 酶联免疫吸附测定, 免疫沉淀, 流式细胞仪
文章摘录数: 1
Published customer image: . ICAM-1 activates PKC but not PKC II in HMVECLs. A ) At 70% confluence, HMVECLs cells pretreated with 10 ng/ml TNF to induce ICAM-1 expression. At 24 hrs, the cells were suspended and immunolabeled with anti-ICAM-1 antibodies and examined by flow cytometry for ICAM-1 expression. B–D) HMVECLs were pretreated with TNF as in panel A. At 24 hrs, the endothelial cells were nonstimulated (NS) or stimulated with a confluent monolayer of anti-ICAM-1-coated beads or the control anti-PECAM-1-coated beads for 20 minutes in B and D or for the times indicated in C. The cells were lysed and the activation of PKC II and PKC was examined by western blot with B) anti-phospho-PKC IIThr641 or anti-PKC II or C–D) anti-phospho- PKC Thr638 or anti-PKC . Shown are representative blots. Shown are the mean SEM of 3 experiments. NT, nontreated. *, p 0.05 as compared to the nontreated (NT) groups. From: Abdala-Valencia H, Berdnikovs S, Cook-Mills JM (2012). Vitamin E Isoforms Differentially Regulate Intercellular Adhesion Molecule-1 Activation of PKC in Human Microvascular Endothelial Cells. PLoS ONE 7(7): e41054 .
规格: 25微克
价格: 88美元
至产商 - 小鼠 单克隆 (84H10)
反应物种: 人类, 狗
应用: 酶联免疫吸附测定, 免疫组化, 免疫沉淀, 流式细胞仪, 免疫组化-冰冻切片
文章摘录数: 3 - 兔 多克隆
反应物种: 人类, 狗
应用: 免疫印迹
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基因信息 - 狗 细胞间粘附分子1
- 同义词:ICAM-1; intercellular adhesion molecule 1; intercellular adhesion molecule 1 (CD54), human rhinovirus receptor
- 描述:intercellular adhesion molecule 1
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- we limit the listing of re-branded antibodies to provide our visitors with accurate information and the best experience
- we manually curate antibody information from the literature to obtain a comprehensive set of well-validated antibodies.
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