这是一篇有关培养基的综述,是根据70篇发表使用实验的文章归纳的。这综述旨在帮助来邦网的访客找到最适合培养基。
同义词: renal Epithelial Basal Medium, McCoy's 5A medium, BGJ medium, PrEC medium, MCDB131 medium, Epilife medium supplemented, T-lymphocyte-conditioned medium, Eagle’s minimum essential medium, Epilife medium supplement, Minimum Essential Medium, minimal essential medium-α, LHC-9 medium, TC100 medium, Iscove's medium, lymphocyte medium, Eagle’s minimal essential medium, Ham's F12 medium, medium 199, tissue freezing medium, N1 growth medium supplement, Eagle's minimal essential medium, Coon's improved medium F-12, tissue-freezing medium, Ham's F-12K medium, serum-free LHC-9 medium, Cellgro ly ...
US BiologicalUS Biological 培养基 产品
为了研究泡状H+-ATPase参与到mTOR通路中mTORC1的转位和激活,采用US Biological的amino acid free Schneiders media进行细胞培养实验。至该文献
赛默飞世尔显示:30; 总数:41
Medium 199培养基被用在细胞培养中,来研究胰腺中平衡生长和内分泌分化的动力学。至该文献
为了研究wnt信号通路在脊髓特性和轴旁中胚层识别过程中的不同作用,采用了Gibco公司的Neurobasal medium培养基,进行细胞培养实验。至该文献
为了研究抗肿瘤反应中Dectin-1的作用,采用了Gibco/Invitrogen公司的McCoy's 5A培养基,进行细胞培养实验。至该文献
为研究癫痫发生能够被NRSF通过基因抑制来调控,采用Life Technologies的Minimal Essential Medium进行脑片培养实验。至该文献
为了研究果蝇中Matrimony表达水平的调控对于卵母细胞-胚胎过渡的重要性,Invitrogen的Schneider血清培养基被用于进行细胞培养实验。至该文献
为了研究Par-1调控组织生长的机制,Invitrogen的果蝇Schneider培养基被用于进行细胞培养。至该文献
为了研究FBW7在Notch信号通路中的作用,Invitrogen的Neurobasal培养基被用于进行细胞培养实验。至该文献
为了研究某些GBM病人有FGFR-TACC融合突变,采用了Invitrogen的neurobasal medium进行细胞培养实验。至该文献
为了研究Dilp8在调控果蝇组织生长中的重要性,Invitrogen的Schneiders完全培养基被用于细胞培养。至该文献
为了研究平面细胞极化对组织形态发生至关重要,采用了Gibco的Schneiders Drosophila Medium进行细胞培养实验。至该文献
为了研究背景记忆的形成依赖海马CA3区npas4依赖的转录程序,采用Invitrogen的Neurobasal A medium进行神经元培养实验。至该文献
为了研究Na(V)1.7基因的变体在非洲裸鼹鼠的酸不敏感中起重要作用,采用Gibco的F-12 Ham medium + L-glutamine进行细胞培养实验。至该文献
为了研究泡状H+-ATPase参与到mTOR通路中mTORC1的转位和激活,采用Invitrogen的Schneiders media进行细胞培养实验。至该文献
为了研究缅甸巨蟒中提取的脂肪酸能够促进心肌的生长,采用Gibco/Invitrogen的Minimum Essential Medium进行细胞培养实验。至该文献
为了研究酵母可以用来模仿Abeta的毒性以筛选可能的修饰基因,采用Life Technologies的Neurobasal medium进行神经元培养实验。至该文献
为了研究S1P蛋白酶对溶酶体的生成至关重要,采用Invitrogen的nutrient mixture F12 Ham进行细胞培养实验。至该文献
为了研究氧化应激条件下DNA修复能被SIRT6通过PARP1活化加强,采用Gibco的EMEM media进行细胞培养实验。至该文献
为了研究剪接体复合物的组装是一个动态有序的过程,采用Fisher Scientific的YPD media进行酵母培养实验。至该文献
为了研究真核生物的强K+输入通道的结构特点,使用了英杰公司的BMGY 培养基来进行细胞培养。至该文献
为了研究Norbin在促代谢型谷氨酸受体5信号途径中所起的调控作用,使用了Gibco公司的Neurobasal培养基来进行细胞培养。至该文献
为了研究Atoh1在小脑发育过程中音速小子蛋白信号途径中所起的作用,使用了英杰公司的Neurobasal培养基来进行细胞培养。至该文献
为了研究E3连接酶对于维持离子稳态所起的作用,使用了Gibco公司的杂交细胞SFM 培养基来进行细胞培养。至该文献
为证实Arf对细胞增殖有限制作用,使用了Fisher Scientific公司的TBS Tissue Freezing Medium来进行组织包埋。至该文献
为了研究BMP4在神经干细胞分化形成神经元过程中所起的作用,使用了Gibco公司的F12培养基来进行皮层细胞的培养。至该文献
为研究粘附分子L1在转内皮迁移和树突状细胞运输过程中所发挥的角色,用英杰公司提供的MCDB 131培养基来培养细胞。至该文献
在研究ARSI基因在人的视网膜色素上皮细胞系ARPE-19的优先表达特性时,采用了英杰的 Ham’s F-12 培养基培养细胞。至该文献
为了证实Bcl-XL对神经元中线粒体的分裂增殖,融合,以及数量有影响,使用了英杰公司的neurobasal培养基来培养神经元。至该文献
为了研究LRRK2的泛素化和降解机制,使用了Invitrogen公司的neurobasal培养基来培养从CD-1小鼠中分离出的小鼠原代皮层神经元。至该文献
为识别APE1的D70在受损3′末端的修复过程中所起的作用并讨论其在催化作用进程中可能存在的意义,用Gibco(英杰)提供的M199培养液来培养细胞。至该文献
为了表明Bmi1基因对神经元的氧化代谢机制所起的调控作用与p53的表达抑制相关联,使用了英杰公司的不含血清的添加有Neurobasal-A的培养基来进行神经元的培养。至该文献
默克密理博中国
为了研究Wee1B在减数分裂中期向后期转变过程中的作用,采用Millipore的M2培养基进行细胞培养。至该文献
西格玛奥德里奇
为了研究DNA代谢能够通过MMS19与胞浆Fe-S复合物相联系,采用了Sigma的M2 medium进行胚胎分离实验。至该文献
为了研究维他命K2的功能,Sigma的Schneider昆虫培养基被用于进行细胞培养。至该文献
为了研究背腹轴受微管介导的卵细胞核移动调控,采用了Sigma的Schneiders medium进行秋水仙碱处理实验。至该文献
为了研究纺锤体装配检验点蛋白在减数第一次分裂过程中所起的作用,使用了西格玛公司的M2培养基来进行卵母细胞培养。至该文献
为了研究ULBP5/RAET1G两种亚型蛋白的特性,细胞内表达及转运,使用西格玛公司的不含甲硫氨酸和半胱氨酸的组织培养基来培养细胞。至该文献
为证实aaMph可以对抗不受控制的大脑感染,使用了西格玛公司的沙氏左旋葡萄糖培养基来进行细胞培养。至该文献
结合计算机模拟实验,模拟实验结果的检验,以及蛋白相互作用网络的反向工程实验来确认新的曲妥单抗抗乳腺癌的潜在治疗策略,用Sigma提供的Leibovitz's L-15培养基来培养MDA-MB-231细胞。至该文献
为研究是否PI3K/PTEN途径在调控Fas 诱导的I型和II型细胞的凋亡过程中有着重要作用,用Sigma Aldrich提供的Histopaque density medium来分离有活力的细胞。至该文献
使用Sigma M2培养液来培育胚泡,来探讨GLUT3在胚胎形成早期发挥重要作用。至该文献
为了揭示DEP-1在促进蛋白激酶活化和延长内皮细胞寿命方面的作用,研究中使用了Sigma公司的MCDB-131培养基来培养HEK 293细胞。至该文献
ATCC
为了研究细螺旋体引起细胞凋亡的分子机制,使用了ATCC公司的F-12K培养基来培养细胞。至该文献
徕卡显微系统(上海)贸易有限公司
为了阐明YB-1蛋白在成年大鼠、猕猴和人大脑中的细胞内分布,使用了Leica Instruments公司的组织冰冻切片包埋剂来包埋脑组织。至该文献
Triangle Biomedical Sciences
为了研究小鼠中器官的正常发育需要B型的核纤层蛋白的功能,采用Triangle Biomedical的tissue freezing medium进行免疫组织化学实验。至该文献
Promocell
Wako Chemicals USA
为了研究神经突触投射能够被软骨酸性蛋白1B通过抑制NgR1来调控,采用Wako的Hams F-12 medium进行鸡DRG神经元培养实验。至该文献
Stemcell Technologies
为研究db/db小鼠在接受db/m小鼠的同源骨髓衍生细胞后的效应,使用了StemCell Technologies公司的MSC培养基来进行细胞培养。至该文献
Krackeler Scientific
为分析系统性红斑狼疮和对照组患者雌激素受体alpha基因多态现象与细胞因子表达间的相关性,用Krackeler Scientific提供的淋巴细胞分离剂来分离单核细胞。至该文献
Lonza
为了研究Vav2和Vav3蛋白在皮肤癌中的作用,Lonza的伊格尔氏最低必需培养基被用于进行细胞培养实验。至该文献
为了研究爪蟾Wnt8与Frizzled8富含半胱氨酸的结构域形成的复合物的结构,采用了Lonza的Schneiders Drosophila medium进行稳定细胞株筛选实验。至该文献
为了研究myc依赖的癌症需要SUMO化修饰来促进肿瘤发生,采用Lonza的mammary epithelial growth medium进行细胞培养实验。至该文献
为了研究人血糖过低可由激活状态的AKT2突变体引起,采用了Lonza的BioWhittaker Ultraculture medium进行病毒制备实验。至该文献
为了研究减毒活疫苗能够激活恶性疟原虫孢子特特异的CD8+免疫细胞而激活免疫反应,采用Lonza的HCMTM hepatocyte culture medium进行PfSPZ侵染能力检测实验。至该文献
为了研究TH2感染会诱发感染处巨噬细胞增殖,采用Lonza Biologics的X-VIVO 15 media进行流式细胞分选实验。至该文献
为了证实对乙酰氨基酚引起肝中毒的两个必需的要素是Tlr9和Nalp3炎症体,使用了Lonza公司的EGM-2 MV Microvascular Endothelial Cell Medium-2来培养窦内皮细胞。至该文献
为了分析EB病毒糖蛋白B的功能结构域,采用了BioWhittaker公司的Ham's F-12培养液产品,进行细胞培养实验。至该文献
Serva
为了研究果蝇中着丝粒的形成能在充分必要因子CENH3的诱导下形成,采用Serva的Schneiders Drosophila medium进行S2细胞培养实验。至该文献
BrainBits
为了研究KLF家族成员对中枢神经系统神经元再生能力的调节,使用了Brainbits公司的Hibernate E培养基来进行细胞培养。至该文献
Welgene
为了证实谷胱甘肽过氧化物酶3能介导人过氧化物酶体增殖激活受体gamma的抗氧化作用,使用了Welgene公司的alpha modified Eagle's medium来培养骨骼肌细胞。至该文献
Cedarlanelabs
为研究是否PI3K/PTEN途径在调控Fas 诱导的I型和II型细胞的凋亡过程中有着重要作用,用Cedarlane提供的Lympholyte-M密度分离液来分离单核细胞。至该文献
Cambrex
为了证实谷胱甘肽过氧化物酶3能介导人过氧化物酶体增殖激活受体gamma的抗氧化作用,使用了Cambrex公司的singleQuots skeletal muscle growth medium来培养骨骼肌细胞。至该文献
文章列表
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- Jessica J Reimer et al. (2009). "Analysis of Epstein-Barr virus glycoprotein B functional domains via linker insertion mutagenesis".PMID 18987135
- Aruna P Ambagala et al. (2009). "Varicella-zoster virus immediate-early 63 protein interacts with human antisilencing function 1 protein and alters its ability to bind histones h3.1 and h3.3".PMID 18971269
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- Kimberly L W Schultz et al. (2009). "Transactivator IE1 is required for baculovirus early replication events that trigger apoptosis in permissive and nonpermissive cells".PMID 18945761
- Catherine Chabot et al. (2009). "New role for the protein tyrosine phosphatase DEP-1 in Akt activation and endothelial cell survival".PMID 18936167
- Sung Soo Chung et al. (2009). "Glutathione peroxidase 3 mediates the antioxidant effect of peroxisome proliferator-activated receptor gamma in human skeletal muscle cells".PMID 18936159
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