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Flow Cytometric Detection of Mitochondrial Membrane Potential 流式细胞术检测线粒体膜电位 作者:Hsin-Yi Chang, Hsuan-Cheng Huang, Tsui-Chin Huang, Pan-Chyr Yang, Yi-Ching Wang and Hsueh-Fen Juan日期:04/20/2013,浏览量:25943,Q&A: 1
Mitochondrial membrane potential (Δψm) is an important parameter of mitochondrial function and an indicator of cell health. Depletion of Δψm suggests the loss of mitochondrial membrane integrity reflecting the initiation of the proapoptotic signal. Recently, lipophilic cationic fluorescent dyes have been developed to detect Δψm by accumulating in ...
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Flow Cytometric Detection of Reactive Oxygen Species 流式细胞术检测活性氧类 作者:Hsin-Yi Chang, Hsuan-Cheng Huang, Tsui-Chin Huang, Pan-Chyr Yang, Yi-Ching Wang and Hsueh-Fen Juan日期:04/20/2013,浏览量:44488,Q&A: 3
Reactive oxygen species (ROS) are molecules containing hydroxyl radicals or peroxides with unpaired electrons. In healthy aerobic cells, ROS are produced naturally as a byproduct of oxidative phosphorylation, oxidoreductase enzymes, or metal catalyzed oxidation at a controlled rate. However, ROS can be induced under some stress conditions ...
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Evaluation of Caspase-1 Activation and IL-1β Production in A Kainic Acid Microdyalisis Brain Injury Model 在红藻氨酸损伤透析模型中评估半胱天冬酶1的活化和IL-1β的产生 作者:Antonio S. Herranz, Eulalia Bazán, Diana Reimers, María T. Montero-Vega, Adriano Jménez-Escrig and Pablo Pelegrín日期:04/20/2013,浏览量:8779,Q&A: 0
Intracerebral infusion of kainic acid (KA) by a microdialysis probe induces a focal swelling in the brain-perfused area which promotes inflammation (Compan et al., 2012; Oprica et al., 2003). The microdialysis technique allows the local in vivo perfusion of KA and the simultaneous collection of inflammatory mediators, ...
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Plasmodium falciparum Rosette Disruption Assay 恶性疟原虫莲座破坏试验 作者:Micheline Guillotte, Odile Mercereau-Puijalon and Inès Vigan-Womas日期:04/20/2013,浏览量:9098,Q&A: 0
Rosetting, i.e. the capacity of Plasmodium falciparum-infected red blood cells (iRBCs) to bind two or more uninfected red blood cells (RBCs) is associated with severe malaria in African children. Disruption of rosettes using small soluble inhibitors or specific antibodies is viewed as an interesting strategy to treat or prevent ...
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Plasmodium falciparum Rosette Formation Assay 恶性疟原虫莲座形成试验 作者:Inès Vigan-Womas, Micheline Guillotte and Odile Mercereau-Puijalon日期:04/20/2013,浏览量:13457,Q&A: 0
Rosetting, i.e. the capacity of red blood cells (iRBCs) infected with mature parasite stages to bind two or more uninfected red blood cells (RBCs) is a virulence factor of Plasmodium falciparum. This protocol describes an in vitro assay to monitor rosette formation by P. falciparum-infected red blood cells, ...
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Packaging of Retroviral RNA into Viral Particles Analyzed by Quantitative Reverse Transcriptase-PCR 通过量化分析RT-qPCR将逆转录病毒RNA整合到病毒颗粒中 作者:Bianca Hoffmann and Bastian Grewe日期:04/20/2013,浏览量:14801,Q&A: 0
Formation of viral particles and packaging of genomic retroviral RNA into these particles are important steps in the late phase of the viral replication cycle. The efficiency of the incorporation of viral or cellular RNAs into viral particles can be studied using a quantitative Reverse Transcriptase-PCR (RT-qPCR)-based approach. After isolation of ...
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High-throughput Method for Determination of Seed Paternity by Microsatellite Markers 利用微卫星标记法高通量鉴定种子亲权 作者:Samik Bhattacharya and Ian T. Baldwin日期:04/20/2013,浏览量:11639,Q&A: 0
In this protocol, determination of seed paternity by microsatellite markers in Nicotiana attenuata is described. However, this does not include a protocol for the novel marker selection/identification, but rather exploits the markers generated for a closely related species N. tabacum (Bindler et al., 2007). This is a ...
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Detection and Cloning of Spliced Transcripts by RT-PCR 采用RT-PCR进行剪切体的检测和克隆 作者:Bianca Hoffmann and Bastian Grewe日期:04/20/2013,浏览量:11622,Q&A: 0
Using a Reverse Transcriptase-PCR approach spliced transcripts can be converted to cDNA, amplified and cloned into an expression plasmid. Sequencing of the obtained cDNA allows identification of the splicing events that generated the detected RNA (Grewe et al., 2012).
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p65 Chromatin Immunoprecipitation Protocol p65染色质免疫共沉淀法 作者:Crissy Dudgeon日期:04/20/2013,浏览量:10157,Q&A: 0
Chromatin Immunoprecipitation (ChIP) is an important procedure that allows you to verify if a certain protein is physically located at a regulatory region. This information, taken together with other procedures such as luciferase assays and EMSAs, will give definitive proof that the query protein is involved in the transcription of a protein. ...
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Primary Culture of Cortical Neurons 皮层神经元的初代培养 作者:Rieko Muramatsu and Toshihide Yamashita日期:04/20/2013,浏览量:23065,Q&A: 2
Primary culture of neurons from cerebral cortex is a popular model to study neuronal function in vitro and to explore the molecular mechanism of neurite outgrowth in the developing and adult central nervous system. This protocol is for preparing a culture of cerebral cortical neurons from postnatal rodent brain (Muramatsu et al., ...
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Culture of Rat Olfactory Ensheathing Cells Using EasySep® Magnetic Nanoparticle Separation 使用EasySep®磁性纳米粒分离法培养大鼠嗅鞘细胞 作者:Susan Louise Lindsay and Susan Carol Barnett日期:04/20/2013,浏览量:8210,Q&A: 0
Olfactory ensheathing cells (OECs) can be isolated and purified from a range of postnatal day 7-day to 10-day rat olfactory bulbs. Rat OECs express the CD271/p75NTR receptor and using the “Do-It-Yourself” magnetic nanoparticle EasySep kit from STEMCELL technologies this protocol allows the selective purification of these cells in less than 50 min. ...
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Determination of Nectar Nicotine Concentration in N. attenuata 烟草花蜜中尼古丁含量的测定 作者:Eva Rothe, Matthias Schöttner, Danny Kessler and Ian T. Baldwin日期:04/20/2013,浏览量:9882,Q&A: 0
In this protocol, the determination of the nicotine concentration in nectar of Nicotiana attenuata is described. This method is applicable for the investigation of small amounts of nectar (above 1 μl). It is a high-throughput protocol optimized and streamlined for one skilled person to process approximately 100 nectar samples per day.
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