这是一篇有关DNA酶I的综述，是根据59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DNA酶I。
赛默飞世尔赛默飞世尔 DNA酶I 产品
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Ambion的DNase1进行RNA提取实验至该文献
为了研究PD-1对IgA选择及肠道菌群组成的调控作用，Invitrogen的DNase I被用于DNA降解。至该文献
为了研究生物钟振荡器相关基因表达可被TOC1抑制，采用了Ambion的RNase-free DNase I进行RNA提取实验。至该文献
为了研究在小鼠中细胞自噬在抗肿瘤化学疗法诱导免疫原性的过程中至关重要，采用Invitrogen的DNase I以150 U/mL浓度进行体内肿瘤消化实验。至该文献
为了研究军团杆菌通过促进真核生物蛋白降解来获得生长所需的氨基酸，采用Ambion的DNase I进行RNA纯化实验。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Invitrogen的RNase-free DNase I进行逆转录实验。至该文献
为了研究大肠杆菌能被被控制形成条纹形状，采用Invitrogen的Amplification Grade DNase I进行RNA纯化实验。至该文献
为了研究真菌在进化过程中为获得和保有杀手病毒而失去RNAi通路，采用Ambion的DNase I进行RNA纯化实验。至该文献
为了研究雌性线虫中的fem-1 RNA能够通过表观遗传学方式对生殖细胞中的基因表达进行调控，采用Ambion的DNaseI进行RNA纯化实验。至该文献
为证实钙调蛋白激活的腺苷酸环化酶对可卡因敏感性形成的重要作用，使用了Fermentas公司的DNase I来除去DNA。至该文献
为研究Lipocalin2蛋白对乳腺癌发展的影响，用英杰公司提供的DNA酶I来处置RNA。至该文献
为证实DCs和GM-CSF可以协同引发维甲酸生成，使用了英杰公司的DNase I来进行细胞分离。至该文献
为了说明X染色体失活不能通过RNA干扰启动，使用了英杰公司的DNA酶I来处理RNA。至该文献
为了研究MEN Epsilon或者beta非编码RNA的功能，使用了英杰公司的DNaseI来除去DNA。至该文献
为证实Vg和（或）Sd的结合会影响Dmef2的活性，使用了Ambion公司的DNase I来除去DNA。至该文献
西格玛奥德里奇
DNase I被用在流式细胞检测中，来研究Huntingtin蛋白在小鼠乳腺上皮细胞的形态发生中对细胞极性形成的作用。至该文献
为了研究LPS运输需要恰当的二硫键重排，采用了Sigma的DNase I以50ug/ml浓度进行外膜分离实验至该文献
为了研究细菌23S rRNA能通过特定修饰逃避TLR13的识别，采用了Sigma的DNase I进行核酸消化实验至该文献
为了研究卵细胞产生过程受MARF1调控，采用了SigmaAldrich的deoxyribonuclease I进行卵母细胞分离实验。至该文献
为了研究特定的骨髓细胞源自卵黄囊，采用了Sigma的DNAse I进行胚胎裂解实验。至该文献
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Sigma的DNaseI以10ug/ml浓度进行细胞裂解实验。至该文献
为了研究脆弱拟杆菌（Bacteroides fragilis）在宿主-微生物共生的建立中的作用，采用Sigma的DNA酶I用于分离淋巴细胞固有层。至该文献
为证实小鼠的T细胞缺失促衰变因子时容易发生肾小球硬化症，使用了西格玛公司的DNA酶I来除去DNA。至该文献
为了证实干扰素gamma对CCL3调停的嗜中性粒细胞的在体内的补充非常关键，把Sigma公司的脱氧核糖核酸酶I加入细胞中五分钟。至该文献
在T细胞发育调节过程中，为了阐明全反式维甲酸对TGF-β-诱导调节的Foxp3和Il10基因的截然相反的作用，采用了Sigma-Aldrich的DNase 1消化脾脏和肠系膜。至该文献
为证实脱氢酶1a1对于造血干细胞和神经干细胞发挥功能是非必需的，使用了西格玛公司的DNase1来进行细胞分离。至该文献
New England Biolabs
为了研究TRPM5活化对人结肠杯状细胞中MUC5AC分泌的调节作用，New England Labs的Dnase I被用于进行DNA消化实验。至该文献
为了研究合成的遗传聚合物的信息存储能力，New England Biolabs的DNase I缓冲液被用于DNA消化。至该文献
为了研究细菌中H-NS能够促进染色体的结构改变，采用New England BioLabs的RNase-free DNase I以40 U/mL浓度进行RNA纯化实验。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NEB的DNA酶I去除DNA。至该文献
上海普洛麦格生物产品有限公司
为了研究生物钟基因表达能够被CIRP进行转录后调控，采用了Promega的RQ1 DNase进行CLIP测序实验。至该文献
为了研究蜜蜂病毒多样性能够被寄生虫瓦螨改变，采用了Promega的DNase I进行RNA纯化实验。至该文献
为了研究基因表达能够通过模型依赖的RNA元件的构建来调控，采用Promega的RQ1 DNase进行RNA纯化实验。至该文献
为了研究兼性异染色质的形成能被mRNA加工因子参与的mRNA降解促进，采用Promega的RNase-free DNase I进行RNA纯化实验。至该文献
为了研究森林中的真菌随着与植物组织的相互作用的改变而不断的多样化，采用Promega的RQ1 DNASE进行RNA提取实验。至该文献
为了研究真核生物中II型拓扑异构酶在正超螺旋DNA影响下发挥DNA解链接的功能，采用Promega的DNase I进行拓扑酶处理实验。至该文献
为了研究细菌第二信使c-di-GMP调节一个别构I型核酶自剪接的机制，使用了Promega公司的RNase-free的DNA酶RQ1来处理分离的总RNA。至该文献
为了说明营养肌动蛋白不同的基因调控及其对植物生长的重要性，使用了Promega公司的RQ1不含RNA酶的DNA酶来处理RNA。至该文献
为了研究脱镁叶绿酸水解酶和叶片衰老和叶绿素分解相关，采用了Promega公司的RQ1 DNase，进行DNA的降解至该文献
为了研究印迹的Dlk1/Pref1基因在个体发育中的剂量效应和后天的致死率对其的影响，使用了Promega公司的不含RNA酶的RQ1 DNA酶来进行反转录定量PCR。至该文献
为了说明HIV-1能够利用imp7来增大其基因组DNA进入细胞核的通道，使用了Promega公司的核酸ReQ1 DNA酶缓冲液来处理样本。至该文献
为了研究斑马鱼白血球中rag1的突变情况，使用了Promega公司的RQ1 RNAse-Free DNase kit来除去DNA。至该文献
Roche Applied Science
为了研究抗肿瘤反应中Dectin-1的作用，采用了Roche Diagnostics公司的DNase I(DNA酶I)，进行组织消化实验。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RocheDNase I和RNase H处理来纯化重组蛋白至该文献
为了研究细菌23S rRNA能通过特定修饰逃避TLR13的识别，采用了Roche的DNase I进行RNA纯化实验至该文献
为了研究发光杆菌科通过单启动子倒置实现致病与共生两种状态的转换，采用了Roche的DNaseI进行RNA提取实验至该文献
为了研究共生菌被先天淋巴细胞限定在特定的位置，采用了Roche的DNase I以20 ug/mL浓度进行流式细胞分选实验。至该文献
为了研究NKT细胞能被早期接触到的微生物调控，采用了Roche的DNase I进行淋巴细胞分离实验。至该文献
为了研究ENT3缺失时会破坏溶酶体的功能和巨噬细胞稳态，采用Roche的DNase 1以20ug/ml浓度进行细胞纯化实验。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Roche的RNAse free DNaseI进行RNA纯化实验。至该文献
为了研究嗜酸粒细胞在代谢平衡调节中的作用，采用Roche的DNA酶I用于组织消化。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，使用了罗氏公司的DNAse I来进行RNA纯化。至该文献
为了研究Eos在Foxp3依赖的基因沉默过程中所起的作用，使用了罗氏公司的DNaseI来除去DNA。至该文献
为研究单核细胞家族谱以及CX3CR1在对抗炎症时所起的作用，使用了罗氏公司的DNase I来消化除去DNA。至该文献
凯杰企业管理（上海）有限公司
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Qiagen公司的DNase I(DNA酶I)，进行DNA消化实验。至该文献
为了研究拟南芥中乙烯介导的生长控制的分子机制，Qiagen的DNaseI被用于进行DNA消化实验。至该文献
为了研究蜜蜂猎奇行为的分子机制，采用了Qiagen Sciences的DNase I进行RNA分离实验。至该文献
为了研究慢性病毒感染的后期IL-6对病毒控制至关重要，采用了Qiagen的DNase I进行RNA提取实验。至该文献
为证实蛋白激酶KIS有助于增强特异mRNAs的翻译活性，使用了Qiagen公司的DNase I来除去DNA。至该文献
GE Healthcare Life Biosciences
为了研究血脑屏障的完整性和中枢神经免疫沉默能够被Shh信号通路促进，采用Amersham Biosciences的DNAse I进行RNA纯化实验。至该文献
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