这是一篇有关Ni-NTA system的综述，是根据69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Ni-NTA system。
默克密理博中国
为了研究AtCERK1能够通过几丁质诱导的二聚化激活，采用了Novagen的Ni-NTA进行蛋白纯化实验。至该文献
赛默飞世尔
为了研究Unc5B and LARG在调控斥性轴突导向分子中的作用，采用了Invitrogen公司的 nickel nitrilotriacetic acid agarose beads产品,来进行蛋白纯化实验。至该文献
为了证实在COMMD1与XIAP通过特定的氨基酸残基连接后可以对COMMD1的基因表达其调控作用，使用了英杰公司的Ni-NTA-Agarose beads来纯化蛋白质以进行蛋白遍在化分析。至该文献
西格玛奥德里奇
为了研究一种新型磷酸位点结合蛋白- TRAF4 在调节紧密连接和促进细胞迁移中的作用，采用了Sigma的His-Select Nickel Affinity Gel纯化重组蛋白。至该文献
为了研究RelA和CBP/p300间的相互作用，Sigma的Ni-NTA柱子被用于进行蛋白质纯化实验。至该文献
为了研究Merlin对神经胶质细胞生长的影响，采用了Sigma公司的组氨酸选择性镍亲和凝胶进行体外蛋白结合分析。至该文献
凯杰企业管理（上海）有限公司显示:30; 总数:44
为了研究HILDA复合物对VEGF-A表达的调控作用，Qiagen的Ni-NTA树脂被用于进行蛋白纯化。至该文献
为了研究MYRF的自剪切机制，Qiagen的Ni-NTA柱被用于进行蛋白纯化实验。至该文献
为了研究荚膜组织胞浆菌温度响应性毒力变化的机制，Qiagen的Ni-NTA琼脂糖珠被用于进行蛋白纯化实验。至该文献
为了研究PI3K gamma的激活机制，Qiagen的Ni2+-NTA琼脂糖被用于进行蛋白质纯化。至该文献
为了研究钙调神经磷酸酶和CAMKII对秀丽隐杆线虫寿命的调节作用，Qiagen的Ni-NTA树脂被用于进行蛋白纯化实验。至该文献
为了研究人类IKK2激活的结构基础,Qiagen的Ni-NTA树脂被用于进行蛋白质纯化实验。至该文献
为了研究alpha-synuclein在诱导突触囊泡类似物聚集中的作用，采用了Qiagen的Ni-NTA affinity resin进行蛋白亲和纯化的实验。至该文献
为了研究二价阳离子对五聚体配体门控离子通道的影响，用了Qiagen镍-NTA层析从表达大肠杆菌膜里提取重组蛋白至该文献
为了研究许多海洋微生物有特定的通路进行甲膦酸合成，采用了Qiagen的Ni-NTA matrix进行蛋白纯化实验至该文献
为了研究MAPK异常活化可被Ste5构象改变隔绝，采用了Qiagen的Ni-NTA进行蛋白纯化实验。至该文献
为了研究Cdc48bullet20S蛋白酶体在古核生物中存在并可能代表着一种古代的AAA+蛋白水解工具，采用了Qiagen的Ni++-NTA agarose进行蛋白纯化实验。至该文献
为了研究隐花色素能够通过特定的小分子激活剂研究，采用了QIAGEN的Ni-NTA Agarose进行蛋白纯化实验至该文献
为了研究终止因子招募会被聚合酶II CTD修饰影响，采用了Qiagen的Ni-NTA column进行蛋白纯化实验。至该文献
为了研究双链RNA可被特定内切酶用于指引DNA切割，采用了Qiagen的Ni-NTA agarose进行蛋白纯化实验。至该文献
为了研究拟南芥中DNA去甲基化可被IDM1调控，采用了Qiagen的Ni columns进行EMSA实验。至该文献
为了利用单分子成像研究肌动蛋白协作装配的机制，采用了Qiagen的Ni2+-NTA-agarose beads进行蛋白纯化实验。至该文献
为了研究Cdc42振荡及其空间分布在裂殖酵母极性生长中的重要性，Invitrogen的Ni-NTA离心柱被用于进行纯化操作。至该文献
为了研究Fam20C参与了胞外蛋白的磷酸化,Qiagen的Ni2+-NTA琼脂糖被用于进行层析操作。至该文献
为了研究RNA长度能够被hnRNP C四聚物识别，采用了Qiagen的Ni-NTA Agarose Beads进行蛋白纯化实验。至该文献
为了研究哺乳动物中NLRP3炎性体能被GBP5调控，采用了Qiagen的NiNTA beads进行蛋白纯化实验。至该文献
为了研究tmRNA-SmpB系统修复停止的核糖体的机制，采用了Qiagen的Ni-NTA column进行蛋白纯化实验。至该文献
为了研究ER蛋白转运需要Sec13p介导的COPII膜的刚性，采用了Qiagen的Ni2+-NTA affinity beads进行蛋白纯化实验。至该文献
为了研究Sir3 BAH与核小体形成的复合物结构是基因沉默的基础，采用Qiagen的NiNTA resin进行蛋白纯化实验。至该文献
为了研究要讲解的tRNA被CCACCA序列标记，采用Qiagen的PQIAexpress Ni-NTA Fast Start kit进行蛋白纯化实验。至该文献
为了研究HIV抗体的效能和作用广度可以通过基于结构的设计进行改善，采用Qiagen的Ni2+-NTA affinity column进行蛋白纯化实验。至该文献
为了利用cIAP1的自身泛素化能够被拮抗剂诱导的cIAP1的构象改变所促进，采用Qiagen的Ni-NTA agarose resin进行蛋白纯化实验。至该文献
为了研究生物钟受JARID1a诱导的CLOCK-BMAL1活化所调控，采用了Qiagen的Ni-NTA进行蛋白纯化实验。至该文献
为了研究大肠杆菌能够被改造后通过密码子编码磷酸化的丝氨酸，采用Qiagen的Ni2+ -NTA resin进行蛋白纯化实验。至该文献
为了研究结核分枝杆菌的反式翻译能够被吡嗪酰胺抑制，采用Qiagen的Ni2+-NTA agarose进行蛋白纯化实验。至该文献
为了通过新发现的中和抗体能够与1型2型流感病毒的血凝素相互作用，采用Qiagen的Ni-NTA resin进行蛋白纯化实验。至该文献
Gold Biotechnology
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Goldbio的Ni2+-NTA affinity resin进行蛋白纯化实验。至该文献
Bio-Rad
为了研究蚊子体内的抗疟原虫免疫是由过氧化物酶/NOX5系统依赖的上皮硝化所介导，采用了Bio-Rad的Profinity Ni-NTA column进行蛋白纯化实验。至该文献
GE Healthcare Life Biosciences
为了研究RasGRP1的调控机制，GE Healthcare的HisTrap FF亲和柱被用于进行蛋白纯化实验。至该文献
为了研究动力蛋白激活蛋白（dynactin）在神经细胞微管的作用, 用了GE Healthcare HisTrap柱来纯化重组蛋白至该文献
为了研究PI3K gamma的激活机制，GE Healthcare的Ni-NTA 5 ml Fast Flow柱子被用于进行蛋白纯化。至该文献
为了研究具核梭杆菌中一种Na+驱动的ATP合成酶的结构和功能属性，GE Healthcare的Ni-NTA琼脂糖凝胶被用于进行蛋白纯化。至该文献
为了研究自组装的蛋白纳米材料可由计算机模拟加以设计，采用了GE Life Sciences的HisTrap HP columns进行蛋白纯化实验。至该文献
为了研究CLOCK:BMAL1转录激活因子复合物的结构，采用了GE Healthcare的Ni Sepharose column进行蛋白纯化实验。至该文献
为了研究乙酰化在自噬调控中的重要性，GE healthcare的Ni2+-NTA琼脂糖被用于蛋白质纯化。至该文献
为了研究AMPK能够被水杨酸直接激活，采用了GE Healthcare的HisTrap column进行蛋白纯化实验。至该文献
为了研究YaeJ修复停止的核糖体的机制，采用了GE Healthcare的5-mL HisTrap HP column进行蛋白纯化实验。至该文献
为了研究alphaB 晶状体蛋白的结构特点，采用了GE Healthcare的5mL HisTrap-HP column进行蛋白纯化实验。至该文献
为了研究eIF4A的解旋酶活性能够被类鼻疽伯克氏菌毒素抑制，采用GE Healthcare的HisTrap FF column进行蛋白纯化实验。至该文献
为了研究Sirt5能够逆转蛋白质赖氨酸的琥珀酰化和丙二酰化，采用GE Healthcare的HisTrapTM HP Column进行蛋白纯化实验。至该文献
为了利用cIAP1的自身泛素化能够被拮抗剂诱导的cIAP1的构象改变所促进，采用GE Healthcare的Ni-affinity column进行蛋白纯化实验。至该文献
为了研究昆虫的内共生体可以被抗菌肽段ColA保护，采用GE Healthcare的HisTrap HP column进行蛋白纯化实验。至该文献
为了研究大肠埃希杆菌（Escherichia coli）完整的核糖体结构，采用GE Healthcare的HisTrap柱纯化蛋白。至该文献
为了研究甲酸盐载体FocA工作模式的转换，采用GE Healthcare的HisTrap柱纯化蛋白。至该文献
为了研究IL-17免疫缺陷会导致慢性皮肤黏膜念珠菌病的发生，采用GE Healthcare的HisTrap HP column进行蛋白纯化实验。至该文献
为了证实硫氧还蛋白DsbG和DsbC可以保护单半胱氨酸不被氧化，使用了GE Healthcare公司的HisTrap HP柱来进行蛋白纯化。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Amersham Biosciences提供的Ni2+-charged HiTrap Chelating HP columns来纯化组氨酸标记的AP内切核酸酶。至该文献
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