淘选
平移(音频)
噬菌体展示
计算生物学
DNA测序
抗体
图书馆
生物
序列(生物学)
克隆(Java方法)
抗体库
序列分析
DNA
基因
肽库
遗传学
肽序列
16S核糖体RNA
古生物学
缩放
镜头(地质)
作者
Aharon Amir,David Taussig,Almog Bitton,Limor Nahary,Anna Vaisman‐Mentesh,Itai Benhar,Yariv Wine
标识
DOI:10.1007/978-1-0716-3381-6_18
摘要
Antibody libraries came into existence 30 years ago when the accumulating sequence data of immunoglobulin genes and the advent of PCR technology made it possible to clone antibody gene repertoires. Phage display (most common) and additional display and screening technologies were applied to pan out desired binding specificities from antibody libraries. As other antibody discovery tools, phage display is not an off-the-shelf technology and not offered as a kit but rather requires experience and expertise for making it indeed very useful.Next-generation sequencing (NGS) coupled with bioinformatics is a powerful tool for analyzing large amount of DNA sequence output of the panning. Here, we demonstrate how NGS analysis of phage biopanning (phage-Seq) of complex antibody libraries can facilitate the antibody discovery process and provide insights regarding the biopanning process (see Fig. 1).
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