IMAGING FACILITY FOR NEUROBIOLOGY

神经生物学成像设备

基本信息

  • 批准号:
    2040544
  • 负责人:
  • 金额:
    $ 23万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    1997
  • 资助国家:
    美国
  • 起止时间:
    1997-05-15 至 1999-05-14
  • 项目状态:
    已结题

项目摘要

With the current application, five faculty in the Division of Neurobiology at the University of Arizona seek to establish a state-of-the-art biological imaging facility to enhance their studies of the development and functional organization of experimentally favorable insect nervous systems. The Division's current Imaging Facility, staffed by a full-time Assistant Staff Scientist, has a Bio-Rad MRC-600 laser scanning confocal microscope, which the five Major Users of this proposal use heavily for NIH-funded research. The MRC-600 is inefficient compared to newer confocal systems and is so popular that one now has to sign up for time 3 - 4 weeks in advance, making the confocal microscope the rate-limiting step in most of our experiments. Moreover, some confocal-microscopy projects have advanced to the point where additional resolution, the capability to visualize fluorescently labeled structures across a broad range of brightness, and the capability to image living preparations over long time periods under very low light levels would enhance our efforts. Therefore, the PI proposes to upgrade the MRC-600 confocal microscope to a MRC-1024, and to purchase a deconvolution microscopy system. The confocal upgrade will provide a larger pixel array for larger fields of view, more filter sets and three photomultiplier tubes for improved detection of multiple fluorophores, and a more efficient computer and software package. Deconvolution, while superficially similar to confocal microscopy in its ability to produce fluorescence images of significantly higher resolution than a standard fluorescence microscope, differs from the confocal microscope in two important ways: rather than rejecting out-of-focus light with a pinhole in the detector, it collects as much light as possible from the objective lenses and uses it to mathematically reconstruct the bright object; and rather than using a photomultiplier tube, which is noisy and whose output is not linearly related to input, it uses a CCD camera for sensitive, linear reporting. Thus, the deconvolution system will meet many of our emerging needs.
根据目前的申请,该部门的五名教员

项目成果

期刊论文数量(0)
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LESLIE P TOLBERT其他文献

LESLIE P TOLBERT的其他文献

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{{ truncateString('LESLIE P TOLBERT', 18)}}的其他基金

DEVELOPMENT OF SEXUALLY DIMORPHIC OLFACTORY GLOMERULI
性二态性嗅球的发育
  • 批准号:
    7090676
  • 财政年份:
    2005
  • 资助金额:
    $ 23万
  • 项目类别:
CORE-- MICROSCOPE FACILITY
核心——显微镜设施
  • 批准号:
    7090680
  • 财政年份:
    2005
  • 资助金额:
    $ 23万
  • 项目类别:
DEVELOPMENT OF SEXUALLY DIMORPHIC OLFACTORY GLOMERULI
性二态性嗅球的发育
  • 批准号:
    6665760
  • 财政年份:
    2002
  • 资助金额:
    $ 23万
  • 项目类别:
CORE-- MICROSCOPE FACILITY
核心——显微镜设施
  • 批准号:
    6665764
  • 财政年份:
    2002
  • 资助金额:
    $ 23万
  • 项目类别:
DEVELOPMENT OF SEXUALLY DIMORPHIC OLFACTORY GLOMERULI
性二态性嗅球的发育
  • 批准号:
    6589570
  • 财政年份:
    2001
  • 资助金额:
    $ 23万
  • 项目类别:
CORE-- MICROSCOPE FACILITY
核心——显微镜设施
  • 批准号:
    6589574
  • 财政年份:
    2001
  • 资助金额:
    $ 23万
  • 项目类别:
CORE-- CONFOCAL AND ELECTRON MICROSCOPY
核心——共焦和电子显微镜
  • 批准号:
    6219174
  • 财政年份:
    1999
  • 资助金额:
    $ 23万
  • 项目类别:
CORE-- CONFOCAL AND ELECTRON MICROSCOPY
核心——共焦和电子显微镜
  • 批准号:
    6273785
  • 财政年份:
    1998
  • 资助金额:
    $ 23万
  • 项目类别:
CORE-- CONFOCAL AND ELECTRON MICROSCOPY
核心——共焦和电子显微镜
  • 批准号:
    6112370
  • 财政年份:
    1998
  • 资助金额:
    $ 23万
  • 项目类别:
CORE-- CONFOCAL AND ELECTRON MICROSCOPY
核心——共焦和电子显微镜
  • 批准号:
    6296942
  • 财政年份:
    1998
  • 资助金额:
    $ 23万
  • 项目类别:

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