在线翻译
The ligation mediated P CR (.. 翻译
原文(英语):
The ligation mediated P CR (L M- PCR) [53] is based on the primer extension of a specific oligonucleotide carried out on a c he mically nicked DNA. A double-strand DNA cassette is t he n ligated to the obtained blunt-end DN A providing the substrate for the final PCR. The linear amplification mediated PCR (LAM-PCR) [54] differs i n the strategy used to obtain the double-strand DNA fragment to ligate with the DNA cassette. In t his case a 5¢ -biotinylated specific primer is ex tended on t he genomic D NA. After capture by strep tavidin beads o f t he ex tension product, a second strand is synthesized by random hexanucleo tide p rim-in g. The double-strand DNA obtained is then digested with a four nucleotide recognizing restriction enzyme and ligated to a p roper DNA cassette. The ligation product i s subjected to a nested PCR amplification, whose product sare further selected by gel electrophoresis analysis 更多:https://www.bmcx.com/ , eluted, re- amplified and sequenced.
翻译结果(简体中文)1:
结扎导带够CR(L M-PCR)[53]的基础上进行交流他mically缺口DNA的一个特定的寡核苷酸引物延伸。双链DNA录像带是他n个连接,得到钝端DN提供最终PCR基板。线性扩增介导的PCR(LAM-PCR)[54]中获得的双链DNA片段的DNA盒结扎的策略不同。他在T 5¢-生物素的特异引物是前上了基因组ðNA倾向。后由的链球菌tavidin珠再三,他当然紧张的产品,第二链合成随机hexanucleo RIM-IN潮P克捕获。获得双股DNA,然后与四核苷酸识别限制性内切酶消化 更多:https://www.bmcx.com/ ,连接到AP罗珀DNA录像带。巢式PCR扩增,凝胶电泳分析,洗脱,重新扩增和测序进一步选择其产品萨雷结扎产品。
翻译结果(简体中文)2:
介导的 P CR (L M-PCR) [53] 基于对 c 进行特定寡核苷酸的底漆扩展名的结扎他 mically 镍 DNA。双链 DNA 卡带是 t n 他扎获得钝端 DN 为最后的聚合酶链反应提供基板。介导聚合酶链反应 (PCR 林) [54] 不同的线性扩增技术我 n 策略用于获取双链 DNA 片段与 DNA 卡带 ligate。T 在他的案件 5、 层层-特定底漆是前往往 t 上他基因组 D na。由他防爆张力产品,第二次的钢绞线由随机 hexanucleo 合成的链球菌 tavidin 珠 o f t 捕捉后潮 p rim 在 g。获得的双链 DNA 与四个核苷酸,认识到限制酶和结扎 p roper DNA 卡带 更多:https://www.bmcx.com/ ,然后消化。结扎产品我遭受嵌套的 PCR 扩增,进一步选定的凝胶电泳分析其产品萨雷 s 洗脱 re-放大和测序。
翻译结果(简体中文)3:
这个结扎介导P CR(L M - PCR)[53]是基于扩展的一个特定的寡核苷酸底漆上执行c他mically刻痕DNA。一个double-strand DNA录音带是t他n元到获得blunt-end DN提供基质为最后的PCR。线性放大介导PCR(LAM-PCR)[54]我在不同策略用来获取double-strand DNA片段与DNA ligate录音带。他的案子在t 5¢-biotinylated特定底漆前往往对t他基因组维娜。链球菌感染后tavidin捕捉珠子o f t他前紧张的产品,第二个主要原因是由随机hexanucleo合成潮汐p rim-in g。double-strand获得的DNA然后消化4核苷酸识别限制性酶和结扎到p roper DNA录音带。我年代的结扎产品受到巢式PCR扩增,其产品sare进一步选择用凝胶电泳分析 更多:https://www.bmcx.com/ ,eluted,再放大和测序。
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