这是一篇有关PCR克隆载体的综述，是根据68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PCR克隆载体。
赛默飞世尔显示:30; 总数:44
为了研究果蝇轴突损伤的胶质细胞反应机制，采用了Invitrogen公司的pENTR/D-TOPO载体，进行DNA克隆实验。至该文献
为了研究果蝇触角叶中Teneurins对突触细胞组织的调控，采用了Invitrogen公司的pENTR/D-TOPO载体，进行DNA克隆实验。至该文献
为了研究减数分裂过程中H3K23甲基化对臂间异染色质的DNA损伤的影响，采用了Life Technologies公司的pENTR-TOPOD载体，进行DNA克隆实验。至该文献
为了研究poly-Ribo-seq在小开放阅读框的翻译过程中的应用，采用了Invitrogen公司的pENTR/D-TOPO载体，进行DNA克隆实验。至该文献
为了研究禽网状内皮组织增生症病毒的起源和进化，Life Technologies的pCR2.1质粒被用于进行DNA克隆。至该文献
为了研究Hedgehog信号通路在神经母细胞增殖和神经发生中的作用，采用Invitrogen公司的pENTR载体进行DNA克隆试验。至该文献
为了研究阿拉伯芥中具有花粉管引诱剂作用的AtLURE1多肽的进化及其功能，采用了Invitrogen的pENTR/D-TOPO载体进行RNAi实验。至该文献
为了研究拟南芥中alpha吡喃酮生物合成的进化，采用了Invitrogen的pENTR1A进行基因扩增实验。至该文献
为了研究损伤引起的轴突死亡需要dSarm/Sarm1信号参与，采用了Invitrogen的pCRII进行原位杂交实验。至该文献
为了研究MORC家族ATP酶的功能特性，Invitrogen的pCR2.1 TOPO载体被用于基因克隆。至该文献
为了研究人胚胎干细胞分化过程中p53的作用，采用了Invitrogen公司的pENTR1a，进行DNA克隆实验。至该文献
为了研究先天免疫对李斯特菌和LPS的应答是通过TNF介导且TNF受iRhom2调控的TACE控制，采用了Invitrogen的pCR2.1-TOPO进行质粒构建实验。至该文献
为了研究许多细菌和古细菌中存在氟核糖开关以抵御氟毒性，采用Invitrogen的pCR2.1 vector进行质粒构建实验。至该文献
为了研究冈崎片段合成过程中DNA聚合酶会在复制叉位置进行更换，采用Invitrogen的pENTR plasmid进行质粒构建实验。至该文献
为了研究同基因型的线虫在应对环境刺激时突变的外显率不同，采用Invitrogen的pENTR 5 TOPO进行质粒构建实验。至该文献
为了研究病原体诱导的拟南芥的细胞器特异性免疫反应需要ESD1参与连接，采用Invitrogen的pENTR/D-TOPO进行质粒构建实验。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Invitrogen的pCR4-TOPO进行质粒构建实验。至该文献
为了研究深海中的几种细菌被发现属于化能无机自养型生物，采用Invitrogen的PCR 2.1进行DNA测序实验。至该文献
为了研究人肿瘤细胞中染色体的异倍性与STAG2的失活相关，采用Invitrogen的pCR-Blunt II-TOPO进行DNA克隆实验。至该文献
为了研究Archaeorhizomycetes的系统发生与进化的特点，采用Invitrogen的pCR4-TOPO进行DNA克隆实验。至该文献
为了研究拟南芥的相互作用组随着环境的改变而演化，采用Invitrogen的pENTR vector进行DNA克隆实验。至该文献
为了研究蝴蝶翅膀花纹拟态的进化受optix基因的调控，采用Invitrogen的pCRII vector进行核酸探针合成实验。至该文献
为了研究塔马尔沙袋鼠产生的甲烷量能被琥珀酸弧苗科细菌降低，采用Invitrogen的pCR4-TOPO进行DNA克隆实验。至该文献
为了研究根毛生长需要细胞壁蛋白发生特定的O糖基化，采用Invitrogen的pCR8/GW/TOPO进行DNA克隆实验。至该文献
为了研究人类样本被重组逆转录病毒XMRV污染，采用Invitrogen的pCR-Blunt进行DNA克隆实验。至该文献
为了研究内含子剪接在发育障碍症MOPD I中的重要作用，采用Invitrogen的pCR2.1 Topo载体用于DNA测序。至该文献
为了揭示Clr4与RNA质量控制复合物之间的联系，采用Invitrogen的pCR-Blunt II-TOPO载体进行质粒构建。至该文献
为了研究一些保守遗传元件在促进C4光合作用进化中的作用，采用Invitrogen的pENTR/D-TOPO载体来构建质粒。至该文献
为了观察鱼鳞病患者中的致病突变基因在体细胞中的丢失，使用了Invitrogen公司的pCR2.1TOPO载体来克隆KRT10的PCR产物。至该文献
为了研究Dnmt3a通过甲基化基因间隔区域调节神经的基因转录和神经发育的功能，使用了Invitrogen公司的pCR4 TOPO载体来亚克隆PCR产物。至该文献
Addgene
为了研究增殖的肝细胞中Par1b诱导质膜区域不对称遗传的机制，采用了Addgene公司的pENTR1A，进行DNA克隆实验。17398至该文献
上海普洛麦格生物产品有限公司
为了研究植物中砷酸盐还原酶在砷累积过程中的作用，采用了Promega公司的T-easy载体，进行DNA克隆实验。至该文献
为研究MID基因对团藻的精子/卵子发育很关键，采用Promega的pGEM-T easy vector进行质粒构建实验。至该文献
为了研究快速发育的脊索动物胚胎中基因的暂时读出表达机制，采用了Promega公司的vector pGEM-T，进行DNA克隆实验。至该文献
为了研究信息素配体是否是基于构象激活的气味结合蛋白，采用了Promega的pGEM-T Easy进行克隆实验。至该文献
为了研究植物中遗传多态性对复杂性状以及适应性的影响，采用了Promega的pGEM-T easy vector进行cDNA克隆实验至该文献
为了研究拟南芥中alpha吡喃酮生物合成的进化，采用了Promega的pGEM-T Easy进行基因扩增实验。至该文献
为了研究动物大脑皮层中含有命运受限的神经前体细胞，采用了Promega的pGEM-T进行探针克隆实验。至该文献
为了研究dll基因在Rheumatobates rileyi两性异形特征进化中的作用，Promega的pGEM-T载体被用于基因克隆。至该文献
为了研究拟南芥中DCL4能够终止转录，采用了Promega的T-easy vector进行质粒构建实验。至该文献
为了研究海洋广古菌门的一种不能培养的细菌基因组能够从宏基因组中抽提出来，采用了Promega的pGEM T-easy vector进行分子克隆实验。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Promega的pGEMT进行基因克隆实验。至该文献
为了研究植物与菌根真菌的共栖通过相互奖励机制加以稳定化，采用Promega的pGEM-T Easy vector system进行DNA克隆实验。至该文献
为了研究果蝇中雌性命运决定受Sxl基因调控，采用Promega的pGEM-T进行cDNA克隆实验。至该文献
为了研究社会阿米巴中亲缘识别是通过tgrB1 与tgrC1的相互作用实现的，采用Promega的pGEM3 plasmid进行DNA克隆实验。至该文献
为了研究克隆副胚层能够用于涡虫再生，采用Promega的pGEM-T Easy vector进行DNA克隆实验。至该文献
为了研究一种能够合成RNA的核酶的进化过程，采用Promega的pGEM-T载体用于DNA测序。至该文献
为了研究秀丽隐杆线虫（C. elegans）融合蛋白家族成员AFF-1蛋白的结构和功能，采用Promega的pGEMT-easy载体构建质粒。至该文献
为了研究果蝇成虫盘中细胞增殖受Dpp蛋白动态变化的影响，采用Promega的pGemTeasy进行DNA克隆实验。至该文献
为了研究转基因真菌被构建出来以杀死携带疟原虫的蚊子，采用Promega的pGEM-T vector进行DNA克隆实验。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Promega公司的pGEM载体 来进行亚克隆。至该文献
使用Promega pGEMT载体来转载鼠AQP2基因 ，来研究细胞水通道的功能。至该文献
为了说明Toll样受体4在革兰氏阴性菌脂多糖信号转导，采用了普洛麦格的的pGEM-T Easy 载体克隆扩增片段。至该文献
为了说明果蝇的Orc蛋白结合到染色体上需要中断有丝分裂周期蛋白依赖性激酶的活性，使用了Promega公司的pGem3Zf(+)载体来转载目的基因。至该文献
为了研究一个转录和组织特异性的印迹肿瘤抑制基因，采用了普洛麦格的pGEM-T Easy载体进行PCR产物的克隆。至该文献
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