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10.1002/0471142956.cy1236s70 http://scihub22266oqcxt.onion/10.1002/0471142956.cy1236s70 C4211606!4211606 !25271959     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=25271959 &cmd=llinks): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 215 Warning: imagejpeg(C:\Inetpub\vhosts\kidney.de\httpdocs\phplern\25271959 .jpg): Failed to open stream: No such file or directory in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 117       Curr+Protoc+Cytom 2014 ; 70 (ä): 12.36.1-10 Nephropedia Template TP {{tp|p=25271959 |t=2014. Correlative fluorescence and electron microscopy |pdf=|usr=}}{{25271959 }} gab.com Text Correlative fluorescence and electron microscopy JO: Curr Protoc Cytom http://www.kidney.de/pget.php?&tw=1&pmid=25271959 #FOAvip Correlative fluorescence and electron microscopy (CFEM) is a multimodal technique that combines dynamic and localization information from fluorescence methods with ultrastructural data from electron microscopy, to give new information about how cellular components change relative to the spatiotemporal dynamics within their environment. In this review, we will discuss some of the basic techniques and tools of the trade for utilizing this attractive research method, which is becoming a very powerful tool for biology labs. The information obtained from correlative methods has proven to be invaluable in creating consensus between the two types of microscopy, extending the capability of each, and cutting the time and expense associated with using each method separately for comparative analysis. The realization of the advantages of these methods in cell biology has led to rapid improvement in the protocols and has ushered in a new generation of instruments to reach the next level of correlation--integration. Twit Text FOAVip Correlative fluorescence and electron microscopy ????Curr Protoc Cytom http://www.kidney.de/pget.php?&tw=1&pmid=25271959 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=25271959 #FOAvip English Wikipedia <ref>{{Cite pmid|25271959 }}</ref> Correlative fluorescence and electron microscopy #MMPMID25271959 Schirra RT Jr ; Zhang P Curr Protoc Cytom 2014[Oct]; 70 (ä): 12.36.1-10 PMID25271959 show ga Correlative fluorescence and electron microscopy (CFEM) is a multimodal technique that combines dynamic and localization information from fluorescence methods with ultrastructural data from electron microscopy, to give new information about how cellular components change relative to the spatiotemporal dynamics within their environment. In this review, we will discuss some of the basic techniques and tools of the trade for utilizing this attractive research method, which is becoming a very powerful tool for biology labs. The information obtained from correlative methods has proven to be invaluable in creating consensus between the two types of microscopy, extending the capability of each, and cutting the time and expense associated with using each method separately for comparative analysis. The realization of the advantages of these methods in cell biology has led to rapid improvement in the protocols and has ushered in a new generation of instruments to reach the next level of correlation--integration. |Animals [MESH] |Humans [MESH] |Microscopy, Electron/*instrumentation/*methods [MESH]Correlative fluorescence and electron microscopy (epmc).pdf DeepDyve Pubget Overpricing