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BRCA1 Antibodies Matter
Breast cancer susceptibility gene 1 (BRCA1) encodes a tumor suppressor that is frequently mutated in familial breast and ovarian cancer patients. BRCA1 functions in multiple important cellular processes including DNA damage repair, cell cycle checkpoint activation, protein ubiquitination, chromatin...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8375228/ https://www.ncbi.nlm.nih.gov/pubmed/34421362 http://dx.doi.org/10.7150/ijbs.63115 |
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author | Yang, Jing Qi, Leilei Chiang, Huai-Chin Yuan, Bin Li, Rong Hu, Yanfen |
author_facet | Yang, Jing Qi, Leilei Chiang, Huai-Chin Yuan, Bin Li, Rong Hu, Yanfen |
author_sort | Yang, Jing |
collection | PubMed |
description | Breast cancer susceptibility gene 1 (BRCA1) encodes a tumor suppressor that is frequently mutated in familial breast and ovarian cancer patients. BRCA1 functions in multiple important cellular processes including DNA damage repair, cell cycle checkpoint activation, protein ubiquitination, chromatin remodeling, transcriptional regulation, as well as R-loop formation and apoptosis. A large number of BRCA1 antibodies have been generated and become commercially available over the past three decades, however, many commercial antibodies are poorly characterized and, when widely used, led to unreliable data. In search of reliable and specific BRCA1 antibodies (Abs), particularly antibodies recognizing mouse BRCA1, we performed a rigorous validation of a number of commercially available anti-BRCA1 antibodies, using proper controls in a panel of validation applications, including Western blot (WB), immunoprecipitation (IP), immunoprecipitation-mass spectrometry (IP-MS), chromatin immunoprecipitation (ChIP) and immunofluorescence (IF). Furthermore, we assessed the specificity of these antibodies to detect mouse BRCA1 protein through the use of testis tissue and mouse embryonic fibroblasts (MEFs) from Brca1(+/+) and Brca1(Δ11/Δ11) mice. We find that Ab1, D-9, 07-434 (for recognizing human BRCA1) and 287.17, 440621, BR-64 (for recognizing mouse BRCA1) are specific with high quality performance in the indicated assays. We share these results here with the goal of helping the community combat the common challenges associated with anti-BRCA1 antibody specificity and reproducibility and, hopefully, better understanding BRCA1 functions at cellular and tissue levels. |
format | Online Article Text |
id | pubmed-8375228 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-83752282021-08-19 BRCA1 Antibodies Matter Yang, Jing Qi, Leilei Chiang, Huai-Chin Yuan, Bin Li, Rong Hu, Yanfen Int J Biol Sci Research Paper Breast cancer susceptibility gene 1 (BRCA1) encodes a tumor suppressor that is frequently mutated in familial breast and ovarian cancer patients. BRCA1 functions in multiple important cellular processes including DNA damage repair, cell cycle checkpoint activation, protein ubiquitination, chromatin remodeling, transcriptional regulation, as well as R-loop formation and apoptosis. A large number of BRCA1 antibodies have been generated and become commercially available over the past three decades, however, many commercial antibodies are poorly characterized and, when widely used, led to unreliable data. In search of reliable and specific BRCA1 antibodies (Abs), particularly antibodies recognizing mouse BRCA1, we performed a rigorous validation of a number of commercially available anti-BRCA1 antibodies, using proper controls in a panel of validation applications, including Western blot (WB), immunoprecipitation (IP), immunoprecipitation-mass spectrometry (IP-MS), chromatin immunoprecipitation (ChIP) and immunofluorescence (IF). Furthermore, we assessed the specificity of these antibodies to detect mouse BRCA1 protein through the use of testis tissue and mouse embryonic fibroblasts (MEFs) from Brca1(+/+) and Brca1(Δ11/Δ11) mice. We find that Ab1, D-9, 07-434 (for recognizing human BRCA1) and 287.17, 440621, BR-64 (for recognizing mouse BRCA1) are specific with high quality performance in the indicated assays. We share these results here with the goal of helping the community combat the common challenges associated with anti-BRCA1 antibody specificity and reproducibility and, hopefully, better understanding BRCA1 functions at cellular and tissue levels. Ivyspring International Publisher 2021-07-25 /pmc/articles/PMC8375228/ /pubmed/34421362 http://dx.doi.org/10.7150/ijbs.63115 Text en © The author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions. |
spellingShingle | Research Paper Yang, Jing Qi, Leilei Chiang, Huai-Chin Yuan, Bin Li, Rong Hu, Yanfen BRCA1 Antibodies Matter |
title | BRCA1 Antibodies Matter |
title_full | BRCA1 Antibodies Matter |
title_fullStr | BRCA1 Antibodies Matter |
title_full_unstemmed | BRCA1 Antibodies Matter |
title_short | BRCA1 Antibodies Matter |
title_sort | brca1 antibodies matter |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8375228/ https://www.ncbi.nlm.nih.gov/pubmed/34421362 http://dx.doi.org/10.7150/ijbs.63115 |
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