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A dataset describing a suite of novel antibody reagents for the RAS signaling network.
Schoenherr, Regine M; Huang, Dongqing; Voytovich, Uliana J; Ivey, Richard G; Kennedy, Jacob J; Saul, Richard G; Colantonio, Simona; Roberts, Rhonda R; Knotts, Joseph G; Kaczmarczyk, Jan A; Perry, Candice; Hewitt, Stephen M; Bocik, William; Whiteley, Gordon R; Hiltke, Tara; Boja, Emily S; Rodriguez, Henry; Whiteaker, Jeffrey R; Paulovich, Amanda G.
Afiliação
  • Schoenherr RM; Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
  • Huang D; Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
  • Voytovich UJ; Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
  • Ivey RG; Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
  • Kennedy JJ; Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
  • Saul RG; Cancer Research Technology Program, Antibody Characterization Lab, Frederick National Laboratory for Cancer Research, Frederick, MD, USA.
  • Colantonio S; Cancer Research Technology Program, Antibody Characterization Lab, Frederick National Laboratory for Cancer Research, Frederick, MD, USA.
  • Roberts RR; Cancer Research Technology Program, Antibody Characterization Lab, Frederick National Laboratory for Cancer Research, Frederick, MD, USA.
  • Knotts JG; Cancer Research Technology Program, Antibody Characterization Lab, Frederick National Laboratory for Cancer Research, Frederick, MD, USA.
  • Kaczmarczyk JA; Cancer Research Technology Program, Antibody Characterization Lab, Frederick National Laboratory for Cancer Research, Frederick, MD, USA.
  • Perry C; Cancer Research Technology Program, Antibody Characterization Lab, Frederick National Laboratory for Cancer Research, Frederick, MD, USA.
  • Hewitt SM; National Cancer Institute, Bethesda, MD, USA.
  • Bocik W; Cancer Research Technology Program, Antibody Characterization Lab, Frederick National Laboratory for Cancer Research, Frederick, MD, USA.
  • Whiteley GR; Cancer Research Technology Program, Antibody Characterization Lab, Frederick National Laboratory for Cancer Research, Frederick, MD, USA.
  • Hiltke T; National Cancer Institute, Bethesda, MD, USA.
  • Boja ES; National Cancer Institute, Bethesda, MD, USA.
  • Rodriguez H; National Cancer Institute, Bethesda, MD, USA.
  • Whiteaker JR; Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
  • Paulovich AG; Fred Hutchinson Cancer Research Center, Seattle, WA, USA. apaulovi@fredhutch.org.
Sci Data ; 6(1): 160, 2019 08 29.
Article em En | MEDLINE | ID: mdl-31467290
RAS genes are frequently mutated in cancer and have for decades eluded effective therapeutic attack. The National Cancer Institute's RAS Initiative has a focus on understanding pathways and discovering therapies for RAS-driven cancers. Part of these efforts is the generation of novel reagents to enable the quantification of RAS network proteins. Here we present a dataset describing the development, validation (following consensus principles developed by the broader research community), and distribution of 104 monoclonal antibodies (mAbs) enabling detection of 27 phosphopeptides and 69 unmodified peptides from 20 proteins in the RAS network. The dataset characterizes the utility of the antibodies in a variety of applications, including Western blotting, immunoprecipitation, protein array, immunohistochemistry, and targeted mass spectrometry. All antibodies and characterization data are publicly available through the CPTAC Antibody Portal, Panorama Public Repository, and/or PRIDE databases. These reagents will aid researchers in discerning pathways and measuring expression changes in the RAS signaling network.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transdução de Sinais / Genes ras / Anticorpos Monoclonais Limite: Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transdução de Sinais / Genes ras / Anticorpos Monoclonais Limite: Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article