（1）桌上只许有笔，答题纸和英文课本。（2）不许 离开自己的座位。（3）不许偷看，不许讲话 (有问题 举手）（4）老师宣布停的时候，必须放下自己的笔。 （5）老师宣布收试卷时，试卷必须快速由每排的最左 边传向右边，每排最右边的同学负责把试卷交给当堂 助教

第一节 转基因动物 Transgenic Animals 第二节 基因打靶（gene targeting） （定向基因转移，基因组靶向编辑） 第三节 新一代基因打靶——基因组编辑技术 第四节 基因打靶在医学中的应用

Companies hire researchers, license ideas, generate much useful data that aren’t always published, and fund scholarships. Famil￾iarity with the corporate mindset, structure and resources can help you obtain what you need and avoid problems you don’t want. All Companies Are the Same?

第一节 概述 第二节 基因治疗的基本流程 一．克隆治疗基因 二．载体的选择与构建 三．选择合适的靶细胞 四．基因转移 五．基因转染细胞的筛选与鉴定 六．回输体内 第三节 基因治疗的临床研究

The principle of the polymerase chain reaction (PCR) was first reported in 1971 (Kleppe et al., 1971), but it was only after the dis￾covery of the thermostable Taq DNA polymerase (Saiki et al., 1988; Lawyer et al., 1989) that this technology became easy to use

troduce different notations. Some consider “NTP” a general term for deoxynucleotides, but the absence of the letter “d” indicates a ribonucleotide to others. Commercial literature also describes ribonucleotides as “RTP’s.” If the letter “d” is present, the name describes a deoxynucleotide. If “d” is absent, check the literature

What Do You Know About Your Target? The sensitivity needs of your system are primarily determined by the abundance of your target, which can be approximated according to its origin. Plasmids, cosmids, phagemids as colony lifts or dot blots, and PCR products are usually intermediate to high-abundance targets. Genomic DNA is considered an intermediate to low-abundance target. Most prokaryotic genes are present as single copies, while genes from higher eukaryotes

Air Buoyancy Akin to water keeping something afloat, samples can be “lifted” by air, artificially decreasing their apparent weight. This air buoy￾ancy can have a significant effect on smaller samples. Electrostatic Forces Electrostatic charges are almost always present in any environ￾ment, particularly in areas with very low humidity. If there are

This book celebrates the importance of the question; it is not meant to be a collection of facts or procedures. The writing of this book was inspired by 16 years of queries from the research community.The con￾tributors and I have tried to meet two primary objectives:

Over the past decade the variety of hosts and vector systems for recombinant protein expression has increased dramatically. Researchers now select from among mammalian, insect, yeast, and prokaryotic hosts, and the number of vectors available for use in these organisms continues to grow