fragment code造句

• The fragment codes the enzyme of 459 amide acids , the molecule weight of which was 49903 . 92dal
  此片段编码由459个氨基酸组成的酶，计算分子量为49903 . 92dal 。
• These diverse encoding schemes forced developers to create fragmented code bases for operating systems and applications , such as single - byte editions for european languages , double - byte editions for asian languages , and bidirectional editions for middle eastern languages
  这些不同的编码方案迫使开发人员为操作系统和应用程序创建零碎的基本代码，如用于欧洲语言的单字节版本、用于亚洲语言的双字节版本以及用于中东语言的双向版本。
• Methods : the rearranged gene fragment coding tcr y v region of the jurkat cell line was obtained by rt - pcr technique the pcr product was cloned into the eukaryocytic expressive vector pcdnas to construct pcdna3 / tcr y . after confirmed by sequncing . pcdnas / tcr y plasmids were amplified in bacteria extracted by alkaline lysismethod
  方法：本文采用rt ? ? pcr的方法扩增jurkatt淋巴瘤细胞特异性重排的tcr可变区基因片段，克隆到真表达载体pcdna _ 3中，经序列测定无误后，碱裂解法大量提取质粒，制备dna疫苗。
• As well as in eukaryocyte ( hepg2 and cos - 7 ) , then detect their antigenity as a basis study and explore of the choice of immunogen for preventive and therapeutic vaccines of hepatitis b . methods : the gene fragments coding 152aa ( si ) and 124aa ( s2 ) of the carboxyl terminus of hbsag were amplified by pcr from plasmid pecob6 with a pair of primers containing different endonuclease sites and were cloned into multiple cloning sites of plasmid pbks ( + )
  为乙型肝炎的预防和治疗性疫苗免疫原的选择进行初步的研究和探讨。方法：本研究利用聚合酶链反应( pcr ) ，通过设计带有不同酶切位点的一对引物，从质粒pecob6特异性扩增hbsag蛋白羧基末端152个氨基酸( s1 )和124个氨基酸( s2 )的基因片段，分别将二者克隆到质粒pbks ( + )的多克隆位点，筛选重组克隆。