Antibodies in proteomics II: screening, high-throughput characterization and downstream applications

被引:46
作者
Bradbury, A
Velappan, N
Verzillo, V
Ovecka, M
Chasteen, L
Sblattero, D
Marzari, O
Lou, JL
Siegel, R
Pavlik, P
机构
[1] Los Alamos Natl Lab, B Div, Los Alamos, NM 87545 USA
[2] Univ Calif San Francisco, Inst Neurodegenerat Dis, San Francisco, CA 94143 USA
[3] Univ Trieste, Dipartimento Biol, I-34127 Trieste, Italy
[4] Univ Calif San Francisco, Dept Anesthesiol, San Francisco, CA 94110 USA
[5] Pacific NW Natl Lab, Richland, WA 99352 USA
关键词
D O I
10.1016/S0167-7799(03)00117-3
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
There are many ways in which the use of antibodies and antibody selection can be improved and developed for high-throughput characterization. Standard protocols, such as immunoprecipitation, western blotting and immunofluorescence, can be used with antibody fragments generated by display technologies. Together with novel approaches, such as antibody chips and intracellular immunization, these methods will yield useful proteomic data following adaptation of the protocols foe increased reliability and robustness. To date, most work has focused on the use of standard, well-characterized commercial antibodies. Such protocols need to be adapted for broader use, for example, with antibody fragments or other binders generated by display technologies, because it is unlikely that traditional approaches will provide the required throughput.
引用
收藏
页码:312 / 317
页数:6
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