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10.3402/jev.v4.26048 http://scihub22266oqcxt.onion/10.3402/jev.v4.26048 C4393420!4393420!25862471     free     free     free Deprecated: Implicit conversion from float 213.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 213.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       J+Extracell+Vesicles 2015 ; 4 (ä): ä Nephropedia Template TP {{tp|p=25862471|t=2015. Potentials and capabilities of the Extracellular Vesicle (EV) Array |pdf=|usr=}}{{25862471}} gab.com Text Potentials and capabilities of the Extracellular Vesicle (EV) Array JO: J Extracell Vesicles http://www.kidney.de/pget.php?&tw=1&pmid=25862471 #FOAvip Extracellular vesicles (EVs) and exosomes are difficult to enrich or purify from biofluids, hence quantification and phenotyping of these are tedious and inaccurate. The multiplexed, highly sensitive and high-throughput platform of the EV Array presented by Jørgensen et al., (J Extracell Vesicles, 2013; 2: 10) has been refined regarding the capabilities of the method for characterization and molecular profiling of EV surface markers. Here, we present an extended microarray platform to detect and phenotype plasma-derived EVs (optimized for exosomes) for up to 60 antigens without any enrichment or purification prior to analysis. Twit Text FOAVip Potentials and capabilities of the Extracellular Vesicle (EV) Array ????J Extracell Vesicles http://www.kidney.de/pget.php?&tw=1&pmid=25862471 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=25862471 #FOAvip English Wikipedia <ref>{{Cite pmid|25862471}}</ref> Potentials and capabilities of the Extracellular Vesicle (EV) Array #MMPMID25862471 Jørgensen MM; Bæk R; Varming K J Extracell Vesicles 2015[]; 4 (ä): ä PMID25862471show ga Extracellular vesicles (EVs) and exosomes are difficult to enrich or purify from biofluids, hence quantification and phenotyping of these are tedious and inaccurate. The multiplexed, highly sensitive and high-throughput platform of the EV Array presented by Jørgensen et al., (J Extracell Vesicles, 2013; 2: 10) has been refined regarding the capabilities of the method for characterization and molecular profiling of EV surface markers. Here, we present an extended microarray platform to detect and phenotype plasma-derived EVs (optimized for exosomes) for up to 60 antigens without any enrichment or purification prior to analysis. äPotentials and capabilities of the Extracellular Vesicle (EV) Array (epmc).pdf DeepDyve Pubget Overpricing