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10.1002/cpch.1 http://scihub22266oqcxt.onion/10.1002/cpch.1 C4940987!4940987 !27258688     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=27258688 &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 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Warning: imagejpeg(C:\Inetpub\vhosts\kidney.de\httpdocs\phplern\27258688 .jpg): Failed to open stream: No such file or directory in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 117       Curr+Protoc+Chem+Biol 2016 ; 8 (2 ): 83-95 Nephropedia Template TP {{tp|p=27258688 |t=2016. Pseudo-Ligandless Click Chemistry for Oligonucleotide Conjugation |pdf=|usr=}}{{27258688 }} gab.com Text Pseudo-Ligandless Click Chemistry for Oligonucleotide Conjugation JO: Curr Protoc Chem Biol http://www.kidney.de/pget.php?&tw=1&pmid=27258688 #FOAvip Particularly for its use in bioconjugations, the copper-catalyzed (or copper-promoted) azide-alkyne cycloaddition (CuAAC) reaction or 'click chemistry', has become an essential component of the modern chemical biologist's toolbox. Click chemistry has been applied to DNA, and more recently, RNA conjugations, and the protocols presented here can be used for either. The reaction can be carried out in aqueous buffer, and uses acetonitrile as a minor co-solvent that serves as a ligand to stabilize the copper. The method also includes details on the analysis of the reaction product. © 2016 by John Wiley & Sons, Inc. Twit Text FOAVip Pseudo-Ligandless Click Chemistry for Oligonucleotide Conjugation ????Curr Protoc Chem Biol http://www.kidney.de/pget.php?&tw=1&pmid=27258688 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=27258688 #FOAvip English Wikipedia <ref>{{Cite pmid|27258688 }}</ref> Pseudo-Ligandless Click Chemistry for Oligonucleotide Conjugation #MMPMID27258688 Mack S ; Fouz MF ; Dey SK ; Das SR Curr Protoc Chem Biol 2016[Jun]; 8 (2 ): 83-95 PMID27258688 show ga Particularly for its use in bioconjugations, the copper-catalyzed (or copper-promoted) azide-alkyne cycloaddition (CuAAC) reaction or 'click chemistry', has become an essential component of the modern chemical biologist's toolbox. Click chemistry has been applied to DNA, and more recently, RNA conjugations, and the protocols presented here can be used for either. The reaction can be carried out in aqueous buffer, and uses acetonitrile as a minor co-solvent that serves as a ligand to stabilize the copper. The method also includes details on the analysis of the reaction product. © 2016 by John Wiley & Sons, Inc. |Alkynes/*chemistry [MESH] |Azides/*chemistry [MESH] |Click Chemistry/*methods [MESH] |DNA/chemistry [MESH] |Oligonucleotides/*chemistry [MESH]Pseudo-Ligandless Click Chemistry for Oligonucleotide Conjugation (epmc).pdf DeepDyve Pubget Overpricing