Request for Ultracryomicrotomy equipment
Request for Ultracryomicrotomy equipment
批准号:
7591904
负责人:
SIMON C WATKINS
金额:
$17.88万
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-04-01 至 2010-03-31
关键词:
16 year oldCellsContractorCryoultramicrotomyDevicesDiseaseElectronicsEquipmentFailureFloorFundingGrantHarvestImageImmunoelectron MicroscopyIndividualLabelLettersMethodsMicrotome - medical deviceMolecularOperative Surgical ProceduresProteinsResearchResolutionRoleRunningServicesSupport SystemSystemTemperatureTimeTissuesUniversitiesWorkbaselight microscopypublic health relevancerepairedtool
中文摘要
描述(由申请人提供):本申请申请资金用于购买两个带有cryokits的超微基因组,用于匹兹堡大学生物成像中心(CBI)的EM设施。使用超薄冷冻切片进行免疫金标记的免疫电子显微镜是CBI提供的一项重要服务,该中心自1991年开始运营以来,已经连续使用了两台超显微切片机。最初,cryokits都是基于两个UltraCut E单元,一个是新的,另一个可以追溯到20世纪80年代初。当其中一个装置出现故障时,它被作为备件保存起来,并在大约13年前被一辆ultraut S Cryokit取代。2年前,s单元制冷机发生了不可修复的故障(徕卡根本不为这些系统提供任何支持,由于电子设备和低温室温度控制的多重故障,独立承包商无法修复该设备)。我们已经设法保持旧的UltraCut E单元运行使用从以前的退役系统中收集的备件,但是这个系统现在已经超过16年的失败,也不能可靠地修复,当然,即使全天使用也不能跟上我们用户群的需求。基本上这个系统也必须退役。我们将继续使用它们作为显微切片机(实际上Ultracut S单元已经完成了这个角色),但我们必须购买2个新的冷冻系统。不幸的是,由于制造过时,这只能通过购买完整的超微切片机和cryokits来完成。重要的是要认识到我们确实需要两个系统,而不是简单地要求两个设备来获得SIG拨款机制的资金上限。在第一次crycryit失败后,我们试图为单个crycrytricroome添加“填充”申请,但我们觉得这有点过分。现在我们处于一个没有双赢的局面,我们必须更换两个系统(校园里没有其他的超染色体组切片机或核心研究EM设施,整个匹兹堡都没有可用的超染色体组切片机)。这一需求在本中心的使用情况描述、个人用户的预计使用情况以及机构高级官员的支持信中得到了定义。公共卫生相关性:使用超薄冷冻切片进行免疫金标记的免疫电子显微镜是准确确定蛋白质在细胞和组织内位置的重要工具。其分辨率至少是光学显微镜的10倍。这种分辨率优势使得该方法通过定义重要分子在细胞内产生和工作的位置,成为理解潜在疾病的分子机制的极其重要的工具。
英文摘要
DESCRIPTION (provided by applicant): This request is for funds to purchase two Ultramicrotomes with cryokits for use in the EM facility within the Center for Biologic Imaging (CBI) at the University of Pittsburgh. Immuno-electron microscopy, using ultrathin cryosections for immunogold labeling, is an essential service provided by the CBI, and the center has had two ultracryomicrotomes in continuous use since it first started operations in 1991. Initially the cryokits were both based around two UltraCut E units, one was new the other dated from the early 1980's. When one of these units failed it was kept for spare parts and replaced with an Ultracut S Cryokit some 13 years ago. 2 years ago the S-unit cryokit failed irreparably (Leica does not provide any support for these systems at all, and independent contractors were unable to repair the device due to multiple failures of the electronics and temperature control of the cryochamber). We have managed to keep the older UltraCut E unit running using spare parts harvested from the previously retired system, however this system which is now over 16 years old is failing and also cannot be repaired reliably, and certainly even with all day usage does not keep up with the needs of our user base. Essentially this system must be retired also. We will continue to use them as microtomes (in fact the Ultracut S unit is already fullfilling this role) but it is imperative we purchase 2 new cryosystems. Unfortunately this can only be done by purchasing complete ultramicrotomes plus cryokits due to manufacturing obsolescence. It is important to realize we really do need two systems, and are not simply requesting two devices to get above the funding floor of the SIG grant mechanism. Following failure of the first cryokit we were tempted to put in a "padded" application for a single cryoultramicrotome, however we felt that would be a little egregious. Now we are in a no-win situation where we must replace two systems (there are no other ultracryomicrotomes or core research EM facilities on campus or functioning ultracryomicrotomes in all of Pittsburgh). This need is defined in the description of the usage of the Center, the projected usage by individual users and in letters of support from senior institutional officials Public Health Relevance: Immuno-electron microscopy, using ultrathin cryosections for immunogold labeling, is an essential tool in defining exactly where proteins are within cells and tissues. The resolution is at least 10 times better than that possible using light microscopy. This resolution advantage makes this method an extremely important tool in understanding the molecular mechanisms underlying disease by defining where molecules of import are made and work within cells.
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