这是一篇有关Phusion DNA Polymerase的综述,是根据36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Phusion DNA Polymerase。
赛默飞世尔
为研究MID基因对团藻的精子/卵子发育很关键,采用Thermo Scientific的Phusion Polymerase进行DNA扩增实验。至该文献
为了研究Myrf对中枢神经系统髓鞘形成的调节作用,Thermo Scientific的Phusion高保真PCR试剂盒被用于进行DNA突变实验。至该文献
为了研究罂粟中包含10个基因的基因簇是生物碱诺司卡品合成所需要的,采用了Finnzymes的Phusion Hot Start DNA Polymerase进行PCR实验。至该文献
为了研究不同生物体中Mp1与Mp2对丙酮酸摄取至关重要,采用了Thermo-Fisher的Hot-Start Phusion Polymerase进行PCR实验。至该文献
为了研究海洋浮游细菌对浮游植物大量繁殖的响应,Finnzymes Oy的Phusion高保真DNA聚合酶被用于进行PCR操作。至该文献
为了研究农业改革对欧洲人基因组变异的影响,Finnzymes的Phusion聚合酶被用于PCR扩增。至该文献
为了研究斑马鱼中miR430能够抑制蛋白翻译,采用了Thermo Scientific的Phusion High-Fidelity DNA Polymerase进行小RNA测序文库制备实验。至该文献
为了研究线虫能够通过谷氨酸门控氯离子通道变异获得抗阿佛菌素能力,采用了Finnzymes的Phusion Site-Directed Mutagenesis Kit进行点突变实验。至该文献
为了研究细菌通过产生H2S来抵抗抗生素危害,采用Finnenzymes的Phusion DNA polymerase进行PCR实验。至该文献
为了用新的筛选方法研究治疗肝脏阶段疟原虫的新一代药物,采用Thermo Fisher Scientific的Phusion polymerase进行PCR实验。至该文献
为了通过对真核生物60S核糖体亚基与eIF6复合体结构的研究揭示它在蛋白翻译中的作用,采用Finnzymes的Phusion DNA polymerase进行PCR实验。至该文献
为了研究慢性疲劳综合征与鼠白血病病毒无关,采用Thermo的Phusion taq进行PCR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Finnzymes的Phusion DNA polymerase进行PCR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Finnzymes的Phusion Polymerase进行PCR实验。至该文献
为了研究裂殖酵母的基因组结构及基因调控,采用Finnzymes的Pfusion热启动高保真DNA聚合酶进行PCR试验。至该文献
为了说明EWS-FLI1蛋白通过与微卫星序列结合来实现其转录激活作用,使用了Finnzymes公司的Phusion DNA聚合酶来扩增接头修饰的DNA片段。至该文献
为了研究桡骨辐头蛋白基因RSPH9 和 RSPH4A在原发性纤毛运动障碍伴随中央微管对异常疾病中的作用,采用了Invitrogen公司的pFusion Taq产品, 进行PCR实验。至该文献
VWR
为了研究S1P蛋白酶对溶酶体的生成至关重要,采用Peqlab Biotechnology的Phusion Polymerase进行DNA突变实验。至该文献
New England Biolabs
为了研究Ldb2a在TGFbeta信号通路稳态控制过程中的作用,采用了NEB公司的Phusion DNA聚合酶,进行DNA扩增实验。至该文献
为了研究拟南芥中控制生物钟的激活蛋白质,采用了Phusion的高保真聚合酶来进行PCR反应。至该文献
为了研究牛痘病毒的免疫逃避机制,采用了NEB的Phusion位点特异性突变试剂盒进行位点特异性突变实验。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New England Biolabs的Phusion DNA polymerase进行PCR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NEB的Phusion Site Direct Mutagenesis kit进行基因突变实验。至该文献
为了研究霍乱弧菌生物膜的结构及形成原理,采用了New England Biolabs的Phusion High-Fidelity DNA polymeras进行DNA处理实验。至该文献
为了研究DNA代谢和基因组完整性由MMS19维持,采用了NEB的Phusion Taq polymerase进行质粒构建实验。至该文献
为了研究卵细胞产生过程受MARF1调控,采用了New England BioLabs的Phusion High-Fidelity PCR Kit进行基因克隆实验。至该文献
为了研究趋同适应背后的分子变化多种多样,采用了New England Biolabs的Phusion enzyme进行PCR实验。至该文献
为了研究极地八爪鱼对温度的适应需要对K+通道进行RNA编辑,采用了New England Biolabs的Phusion DNA polymerase进行PCR实验。至该文献
为了研究蓝藻细菌有全新的酶来构建不同的三羧酸循环,采用New England Biolabs的Phusion DNA polymerase进行PCR实验。至该文献
为了研究DNA损伤能够被大肠杆菌复制复合体所忍受,采用NEB的Phusion DNA polymerase进行PCR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New England Biolabs的Phusion DNA Polymerase进行基因打靶实验。至该文献
为了研究少突神经胶质瘤会因为CIC和FUBP1的突变而引发,采用NEB的Hotstart Phusion polymerase进行PCR实验。至该文献
为了通过外显子测序研究NOTCH1突变与头颈部鳞状细胞癌相关,采用NEB的Hotstart Phusion polymerase进行PCR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New England Biolabs的Phusion High-Fidelity PCR master mix进行DNA扩增实验。至该文献
为了研究Hippo信号通路在调控哺乳动物心脏大小中的作用,采用New England Biolabs的Phusion高保真聚合酶进行DNA扩增。至该文献
为了研究拟南芥中异硫氰酸烯丙酯介导的非寄主抗性能被假单胞菌sax基因产物阻断,采用New England Biolabs的Phusion DNA polymerase进行DNA克隆实验。至该文献
文章列表
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- Helena Bujalka et al. (2013). "MYRF is a membrane-associated transcription factor that autoproteolytically cleaves to directly activate myelin genes".PMID 23966833
- Polly Yingshan Hsu et al. (2013). "Accurate timekeeping is controlled by a cycling activator in Arabidopsis".PMID 23638299
- William H McCoy et al. (2012). "Structural mechanism of ER retrieval of MHC class I by cowpox".PMID 23209377
- Kasavajhala V S K Prasad et al. (2012). "A gain-of-function polymorphism controlling complex traits and fitness in nature".PMID 22936775
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- Joseph T P Yeeles et al. (2011). "The Escherichia coli replisome is inherently DNA damage tolerant".PMID 21998391
- Graham Simmons et al. (2011). "Failure to confirm XMRV/MLVs in the blood of patients with chronic fatigue syndrome: a multi-laboratory study".PMID 21940862
- David A Solomon et al. (2011). "Mutational inactivation of STAG2 causes aneuploidy in human cancer".PMID 21852505
- Chetan Bettegowda et al. (2011). "Mutations in CIC and FUBP1 contribute to human oligodendroglioma".PMID 21817013
- Nishant Agrawal et al. (2011). "Exome sequencing of head and neck squamous cell carcinoma reveals inactivating mutations in NOTCH1".PMID 21798897
- Katrin Marschner et al. (2011). "A key enzyme in the biogenesis of lysosomes is a protease that regulates cholesterol metabolism".PMID 21719679
- Shigenori Hirose et al. (2011). "Self-recognition in social amoebae is mediated by allelic pairs of tiger genes".PMID 21700835
- Tobias Paprotka et al. (2011). "Recombinant origin of the retrovirus XMRV".PMID 21628392
- Daniel E Wagner et al. (2011). "Clonogenic neoblasts are pluripotent adult stem cells that underlie planarian regeneration".PMID 21566185
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