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J Proteome Res. 2017 Jan 6;16(1):147-155. doi: 10.1021/acs.jproteome.6b00821. Epub 2016 Oct 26.

Antibody Validation in Bioimaging Applications Based on Endogenous Expression of Tagged Proteins.

Author information

1
Science for Life Laboratory, Royal Institute of Technology , SE-114 28 Stockholm, Sweden.
2
Molecular Cell Biology and Genetics, Max Planck Institute , D- 01307 Dresden, Germany.

Abstract

Antibodies are indispensible research tools, yet the scientific community has not adopted standardized procedures to validate their specificity. Here we present a strategy to systematically validate antibodies for immunofluorescence (IF) applications using gene tagging. We have assessed the on- and off-target binding capabilities of 197 antibodies using 108 cell lines expressing EGFP-tagged target proteins at endogenous levels. Furthermore, we assessed batch-to-batch effects for 35 target proteins, showing that both the on- and off-target binding patterns vary significantly between antibody batches and that the proposed strategy serves as a reliable procedure for ensuring reproducibility upon production of new antibody batches. In summary, we present a systematic scheme for antibody validation in IF applications using endogenous expression of tagged proteins. This is an important step toward a reproducible approach for context- and application-specific antibody validation and improved reliability of antibody-based experiments and research data.

KEYWORDS:

Cell Atlas; GFP; Human Protein Atlas; antibody validation; confocal microscopy; immunofluorescence; spatial proteomics; subcellular localization

PMID:
27723985
DOI:
10.1021/acs.jproteome.6b00821
[Indexed for MEDLINE]

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