异氰酸

Total RNA extracted by improved guanidine thiocyanate method and treated with DNaseⅠwere found to be applicable to mRNA differential display technique.

提出了一种有效的芸芥总RNA提取和纯化方法改进异硫氰酸胍法提取的总RNA经DNaseⅠ处理后完全适用于DDRT-PCR分析。

In order to find high active pesticide containing heterocycle, six novel terephthaloyl bisthioureas containing 1, 3, 4-thiodiazole were synthesized by the reaction of 2-amino-5-alkyl-1, 3, 4-thiodiazoles with terephthaloyl diisothiocyanate.

摘 要：为寻找高活性的含杂环农药，由中间体5-烷基-2-氨基-1， 3， 4-噻二唑与对苯二甲酰基二异硫氰酸酯反应，合成6种新的含1， 3， 4-噻二唑环的对苯二甲酰基双硫脲化合物Ⅲaf。

In order to find high active pesticide containing heterocycle, six novel terephthaloyl bisthioureas Ⅲ(subscript a-f containing 1,3,4-thiodiazole were synthesized by the reaction of 2-amino-5-alkyl-1,3,4-thiodiazoles with terephthaloyl diisothiocyanate.

为寻找高活性的含杂环农药，由中间体5-烷基－2-氨基－1，3，4-噻二唑与对苯二甲酰基二异硫氰酸酯反应，合成6种新的含1，3，4-噻二唑环的对苯二甲酰基双硫脲化合物Ⅲ。

Lysis solutions from imported and domestic genomic DNA purification kits,and 2% Trition X-100 and 5%guanidinium isothiocyanate were added into the oocysts,followed by different combining forms of freeze-thawing,proteinase K and sonication.Real-time PCR was used to determine the copies of Cryptosporidium oocyst wall protein gene.HCT-8 cells were infected by C.andersoni oocysts.Real-time PCR was used to determine the enhancement effect of fetal calf serum,glucose,ascorbic acid,folic acid,calcium pantothenate and insulin while added into RPMI-1640 medium.

在隐孢子虫卵囊悬液中分别加入进口试剂盒和国产试剂盒的裂解液以及2%Triton X-100和5%异硫氰酸胍，辅以不同组合方式使用的冻融法、蛋白酶K法和声裂法裂解卵囊，通过Real-time PCR法测定裂解产物中隐孢子虫卵囊囊壁蛋白(Cryptosporidium oocyst wall protein，COWP)基因拷贝数。

The mass fraction of isocyanurate was calculated by piperidine method.

采用六氢吡啶法测出了异氰腺酸酯的质量分数。

The total RNA was isolated from pokeweed leaves using the method of guanidine isothiocyante and used as template for amplification of the deleted mutant pokeweed antiviral protein gene by RT-PCR and then the amplified fragment was cloned into secreted expression pPIC9K vector to form pPIC9K-p, then the vector was transferred into Pachia pastoris GS115 strain.

从美洲商陆叶片中通过异硫氰酸胍法提取出了总RNA，经RT-PCR扩增出缺失突变型抗病毒蛋白PAP基因，将该基因克隆于分泌型真核表达载体pPIC9K，然后导入毕赤酵母菌株GS115细胞。

The method is based on the oxidation-reduction reaction between potassium iodide and nitrite.

建立了碘化钾与亚硝酸根氧化还原反应生成游离碘使异硫氰酸荧光素荧光猝灭测定痕量亚硝酸根的新方法。

According to the prior research , a highly efficient ext raction method was modified1 High2concent ration and DNA 2f ree RNA could be attained by using CTAB/ Guanidine Thiocyanate ext racion buffer1The total RNA can reach 1.7～2.0 of the OD260/ OD280 ratio with the yield of more than 015mg per gram of f resh tissues1 The method is suitable for high2quailty total RNA ext raction in leaves , root s , corollas , seeds and developing fibers.

本研究在前人方法的基础上对快速提取棉花组织总RNA 的方法进行了探讨。利用改进的CTAB 异硫氰酸胍裂解缓冲液，获得的RNA完整性好，无 DNA 污染，含量高，每克鲜组织能提取015mg 总RNA ， OD260/ OD280比值均在117～210之间。

All single step method and CTAB method did not work well when banana total RNA was isolated, unless modified single step method was used, in which, polysaccharide was removed by aether extraction prior to RNA precipitation.

对于富含多糖的香蕉果肉，一步法和CTAB异硫氰酸胍法的效果均不理想；改良后的一步法中增加了乙醚去除多糖并获得了较好的效果。

The total RNA were extracted from CDV infected DK cells or the tissues of infected animals by single step method of acid guanidinium thiocyanate-phenol-chloroform extraction and was used for reverse transcription.

用异硫氰酸胍-酚-仿一步抽提法提取细胞总RNA进行反转录，再以此产物为模板进行PCR扩增，筛选出最佳扩增条件。

The split between the two groups can hardly be papered over.

这两个团体间的分歧难以掩饰。

This approach not only encourages a greater number of responses, but minimizes the likelihood of stale groupthink.

这种做法不仅鼓励了更多的反应，而且减少跟风的可能性。