在大脑中使用绿色荧光蛋白进行研究。 - Suppr

Working with GFP in the brain.

作者信息

Doyle Kristian P, Simon Roger P, Snyder Aurelie, Stenzel-Poore Mary P

机构信息

Department of Molecular Microbiology and Immunology, Oregon Health and Science University, 3181 Sam Jackson Park Road, Portland, OR 97239, USA.

出版信息

Biotechniques. 2003 Mar;34(3):492-4. doi: 10.2144/03343bm08.

DOI:10.2144/03343bm08

PMID:12669698

Abstract

摘要

相似文献

Working with GFP in the brain.

Biotechniques. 2003 Mar;34(3):492-4. doi: 10.2144/03343bm08.

Spinning disk confocal microscope system for rapid high-resolution, multimode, fluorescence speckle microscopy and green fluorescent protein imaging in living cells.

Methods Enzymol. 2003;360:597-617. doi: 10.1016/s0076-6879(03)60130-8.

Optical sectioning by two-pinhole confocal fluorescence microscopy.

Micron. 2003;34(6-7):313-8. doi: 10.1016/s0968-4328(03)00057-x.

Recent advances using green and red fluorescent protein variants.

Appl Microbiol Biotechnol. 2007 Nov;77(1):1-12. doi: 10.1007/s00253-007-1131-5. Epub 2007 Aug 18.

Predicted spatial resolution of super-resolving fluorescence microscopy using two-color fluorescence dip spectroscopy.

Appl Spectrosc. 2003 Oct;57(10):1312-6. doi: 10.1366/000370203769699234.

Toward fluorescence nanoscopy.

Nat Biotechnol. 2003 Nov;21(11):1347-55. doi: 10.1038/nbt895.

Expansion microscopy with conventional antibodies and fluorescent proteins.

Nat Methods. 2016 Jun;13(6):485-8. doi: 10.1038/nmeth.3833. Epub 2016 Apr 11.

Resolution doubling in fluorescence microscopy with confocal spinning-disk image scanning microscopy.

Proc Natl Acad Sci U S A. 2013 Dec 24;110(52):21000-5. doi: 10.1073/pnas.1315858110. Epub 2013 Dec 9.

Identifying and quantitating neural stem and progenitor cells in the adult brain.

Methods Cell Biol. 2008;85:243-72. doi: 10.1016/S0091-679X(08)85011-X.

A new configuration of the Zeiss LSM 510 for simultaneous optical separation of green and red fluorescent protein pairs.

Cytometry A. 2006 Aug 1;69(8):920-9. doi: 10.1002/cyto.a.20323.

引用本文的文献

Spectral Characteristics of Autofluorescence in Renal Tissue and Methods for Reducing Fluorescence Background in Confocal Laser Scanning Microscopy.

J Fluoresc. 2018 Mar;28(2):561-572. doi: 10.1007/s10895-018-2217-4. Epub 2018 Mar 20.

Elimination of autofluorescence background from fluorescence tissue images by use of time-gated detection and the AzaDiOxaTriAngulenium (ADOTA) fluorophore.

Anal Bioanal Chem. 2013 Feb;405(6):2065-75. doi: 10.1007/s00216-012-6623-1. Epub 2012 Dec 20.

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Working with GFP in the brain.

作者信息

Doyle Kristian P, Simon Roger P, Snyder Aurelie, Stenzel-Poore Mary P

机构信息

Department of Molecular Microbiology and Immunology, Oregon Health and Science University, 3181 Sam Jackson Park Road, Portland, OR 97239, USA.

出版信息

Biotechniques. 2003 Mar;34(3):492-4. doi: 10.2144/03343bm08.

DOI:10.2144/03343bm08

PMID:12669698

Abstract

摘要

相似文献

Working with GFP in the brain.

Biotechniques. 2003 Mar;34(3):492-4. doi: 10.2144/03343bm08.

Spinning disk confocal microscope system for rapid high-resolution, multimode, fluorescence speckle microscopy and green fluorescent protein imaging in living cells.

Methods Enzymol. 2003;360:597-617. doi: 10.1016/s0076-6879(03)60130-8.

Optical sectioning by two-pinhole confocal fluorescence microscopy.

Micron. 2003;34(6-7):313-8. doi: 10.1016/s0968-4328(03)00057-x.

Recent advances using green and red fluorescent protein variants.

Appl Microbiol Biotechnol. 2007 Nov;77(1):1-12. doi: 10.1007/s00253-007-1131-5. Epub 2007 Aug 18.

Predicted spatial resolution of super-resolving fluorescence microscopy using two-color fluorescence dip spectroscopy.

Appl Spectrosc. 2003 Oct;57(10):1312-6. doi: 10.1366/000370203769699234.

Toward fluorescence nanoscopy.

Nat Biotechnol. 2003 Nov;21(11):1347-55. doi: 10.1038/nbt895.

Expansion microscopy with conventional antibodies and fluorescent proteins.

Nat Methods. 2016 Jun;13(6):485-8. doi: 10.1038/nmeth.3833. Epub 2016 Apr 11.

Resolution doubling in fluorescence microscopy with confocal spinning-disk image scanning microscopy.

Proc Natl Acad Sci U S A. 2013 Dec 24;110(52):21000-5. doi: 10.1073/pnas.1315858110. Epub 2013 Dec 9.

Identifying and quantitating neural stem and progenitor cells in the adult brain.

Methods Cell Biol. 2008;85:243-72. doi: 10.1016/S0091-679X(08)85011-X.

A new configuration of the Zeiss LSM 510 for simultaneous optical separation of green and red fluorescent protein pairs.

Cytometry A. 2006 Aug 1;69(8):920-9. doi: 10.1002/cyto.a.20323.

引用本文的文献

Spectral Characteristics of Autofluorescence in Renal Tissue and Methods for Reducing Fluorescence Background in Confocal Laser Scanning Microscopy.

J Fluoresc. 2018 Mar;28(2):561-572. doi: 10.1007/s10895-018-2217-4. Epub 2018 Mar 20.

Elimination of autofluorescence background from fluorescence tissue images by use of time-gated detection and the AzaDiOxaTriAngulenium (ADOTA) fluorophore.

Anal Bioanal Chem. 2013 Feb;405(6):2065-75. doi: 10.1007/s00216-012-6623-1. Epub 2012 Dec 20.

Working with GFP in the brain.

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Working with GFP in the brain.

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