快速分析和定量蛋白质在高通量使用PAIA测定

Christine I Wosnitza, Sebastian Giehring, K. Lechner
{"title":"快速分析和定量蛋白质在高通量使用PAIA测定","authors":"Christine I Wosnitza, Sebastian Giehring, K. Lechner","doi":"10.5281/zenodo.31147","DOIUrl":null,"url":null,"abstract":"The PAIA technology provides a novel modular platform for the quantification of proteins. It combines the advantages of bead-based immunoassays with sensitive fluorescence detection in a simple, automation-friendly workflow. The no-wash assays can be processed in one hour per plate and are measured on fluorescence plate readers or microscopes. The amount of sample required is very small, typically 2 10 μL. Thus, the assays are particularly suitable for high throughput antibody and protein quantification in samples like cell culture supernatants. The modular nature of the patent pending PAIA technique offers the possibility to address a large number of analytes.","PeriodicalId":315352,"journal":{"name":"Basel Life Science Week","volume":"17 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2015-09-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Rapid analysis and quantification of proteins in high throughput using PAIA assays\",\"authors\":\"Christine I Wosnitza, Sebastian Giehring, K. Lechner\",\"doi\":\"10.5281/zenodo.31147\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The PAIA technology provides a novel modular platform for the quantification of proteins. It combines the advantages of bead-based immunoassays with sensitive fluorescence detection in a simple, automation-friendly workflow. The no-wash assays can be processed in one hour per plate and are measured on fluorescence plate readers or microscopes. The amount of sample required is very small, typically 2 10 μL. Thus, the assays are particularly suitable for high throughput antibody and protein quantification in samples like cell culture supernatants. The modular nature of the patent pending PAIA technique offers the possibility to address a large number of analytes.\",\"PeriodicalId\":315352,\"journal\":{\"name\":\"Basel Life Science Week\",\"volume\":\"17 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2015-09-18\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Basel Life Science Week\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.5281/zenodo.31147\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Basel Life Science Week","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5281/zenodo.31147","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

paa技术为蛋白质定量提供了一种新的模块化平台。它结合了基于头部的免疫测定和敏感的荧光检测的优点,在一个简单的,自动化友好的工作流程。免洗测定可以在一个小时内处理每个板,并在荧光板阅读器或显微镜上测量。所需的样品量非常小,通常为2 10 μL。因此,该方法特别适用于细胞培养上清等样品中的高通量抗体和蛋白质定量。正在申请专利的PAIA技术的模块化特性提供了处理大量分析物的可能性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Rapid analysis and quantification of proteins in high throughput using PAIA assays
The PAIA technology provides a novel modular platform for the quantification of proteins. It combines the advantages of bead-based immunoassays with sensitive fluorescence detection in a simple, automation-friendly workflow. The no-wash assays can be processed in one hour per plate and are measured on fluorescence plate readers or microscopes. The amount of sample required is very small, typically 2 10 μL. Thus, the assays are particularly suitable for high throughput antibody and protein quantification in samples like cell culture supernatants. The modular nature of the patent pending PAIA technique offers the possibility to address a large number of analytes.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信