{"id":2193,"date":"2015-04-28T08:12:50","date_gmt":"2015-04-28T08:12:50","guid":{"rendered":"http:\/\/www.neb-online.fr\/?page_id=2193"},"modified":"2022-08-03T16:12:21","modified_gmt":"2022-08-03T14:12:21","slug":"in-vitro-rna-synthesis","status":"publish","type":"page","link":"https:\/\/www.neb-online.fr\/en\/rna-biology\/in-vitro-rna-synthesis\/","title":{"rendered":"In vitro RNA Synthesis"},"content":{"rendered":"<div class=\"wpb-content-wrapper\"><p>[vc_row][vc_column width=&#8221;1\/2&#8243;][vc_column_text]<\/p>\n<h2>Background<\/h2>\n<p><em>In vitro<\/em>\u00a0synthesis of single-stranded RNA molecules is a routine laboratory procedure that is essential to the rapidly developing field of RNA research. This technique is versatile in that it allows the researcher to tailor synthesis, and introduce modifications that produce a transcript that is optimal for use in downstream applications. Though the ways in which RNA can be produced are countless, the same basic procedure is followed in all synthesis protocols.[\/vc_column_text][\/vc_column][vc_column width=&#8221;1\/4&#8243;][vc_column_text]<\/p>\n<p style=\"text-align: center;\">&#8220;RNA Synthesis &#8211; From Template to Transcript&#8221;<\/p>\n<p>[\/vc_column_text]<a class=\"btn btn-standard form-btn\"  href=\"https:\/\/www.neb-online.fr\/en\/doc-request\/\" style=\"margin-left:auto;margin-right:auto;\">Order Brochure<\/a>[\/vc_column][vc_column width=&#8221;1\/4&#8243;][vc_single_image image=&#8221;1373&#8243; img_size=&#8221;full&#8221; alignment=&#8221;center&#8221; style=&#8221;vc_box_shadow&#8221; onclick=&#8221;custom_link&#8221; img_link_target=&#8221;_blank&#8221; link=&#8221;http:\/\/www.neb-online.fr\/shop\/loadbalancer.php\/4DCGI\/ezshop?hid=61&amp;sprachnr=2&amp;WorldNr=01&amp;action=sendhtml&amp;htmlpage=infobestellung.htm&#8221;][\/vc_column][\/vc_row][vc_row][vc_column][vc_separator][\/vc_column][\/vc_row][vc_row][vc_column][vc_column_text]<\/p>\n<h2>Workflow\u00a0Details<\/h2>\n<h3>Template Generation<\/h3>\n<p>The first step in\u00a0<em>in vitro<\/em>\u00a0RNA synthesis is to prepare the DNA template corresponding to the sequence of interest. To allow run off transcription, plasmid DNA template is generally linearized with a\u00a0<a title=\"Restriction Enzymes\" href=\"http:\/\/www.neb-online.fr\/en\/neb-en\/cloning-synthetic-biology\/restriktionsenzyme\/\">restriction enzyme<\/a>. In addition to plasmid DNA, PCR products and synthetic oligonucleotides can be used as templates for transcription reactions. We recommend <a title=\"Q5 High Fidelity DNA Polymerase\" href=\"http:\/\/www.neb-online.fr\/en\/neb-en\/pcr-and-dna-amplification\/high-fidelity-pcr\/q5-high-fidelity-dna-polymerase\/\">Q5 High-Fidelity DNA Polymerase<\/a>\u00a0if you plan to use a PCR product as template.<\/p>\n<h3><em>In vitro<\/em>\u00a0 Synthesis<\/h3>\n<p>The template DNA is transcribed by a T7, T3 or SP6 RNA phage polymerase in the presence of ribonucleoside triphosphates (rNTPs). The polymerase traverses the template strand and uses base pairing with the DNA to synthesize a complementary RNA strand (using uracil in the place of thymine). The RNA polymerase travels from the 3&#8242; \u2192 5&#8242; end of the DNA template strand, to produce an RNA molecule in the 5&#8242; \u2192 3&#8242; direction.<\/p>\n<p>The\u00a0<a href=\"https:\/\/shop.neb-online.fr\/en\/art\/E2050@\" target=\"_blank\" rel=\"noopener noreferrer\">HiScribe\u2122 T7 Quick High Yield RNA Synthesis Kit<\/a>\u00a0is designed for quick set-up and production of large amounts of RNA in vitro. The reaction can be set up conveniently by combining the NTP buffer mix, T7 RNA Polymerase mix and a suitable DNA template. The kit also allows for capped RNA or dye-labeled RNA synthesis by incorporation of cap analog (<a href=\"https:\/\/shop.neb-online.fr\/en\/art\/S1411@\" target=\"_blank\" rel=\"noopener noreferrer\">ARCA<\/a>) or dye-modified nucleotides. The\u00a0<a href=\"https:\/\/shop.neb-online.fr\/en\/art\/E2040@\" target=\"_blank\" rel=\"noopener noreferrer\">HiScribe\u2122 T7 High Yield RNA Synthesis Kit<\/a>\u00a0is an extremely flexible system for\u00a0<em>in vitro<\/em>\u00a0transcription of RNA using T7 RNA Polymerase. The kit allows for synthesis many kinds of RNA including internally labeled and co-transcriptionally capped<\/p>\n<h3>Combined\u00a0RNA Synthesis and Modification<\/h3>\n<p>For combined RNA synthesis and modification NEB offers the\u00a0<a href=\"https:\/\/shop.neb-online.fr\/en\/art\/E2065@\" target=\"_blank\" rel=\"noopener noreferrer\">HiScribe\u2122 T7 ARCA mRNA Kit<\/a>\u00a0and the\u00a0<a href=\"https:\/\/shop.neb-online.fr\/en\/art\/E2060@\" target=\"_blank\" rel=\"noopener noreferrer\">HiScribe\u2122 T7 ARCA mRNA Kit (with tailing)<\/a>.<br \/>\nBoth kits include reagents need for RNA synthesis, modification and clean-up.transcripts.<\/p>\n<h3><span style=\"line-height: 1.5;\">RNA Modification<\/span><\/h3>\n<p>mRNAs synthesized\u00a0<em>in vivo<\/em>\u00a0by eukaryotic organisms are cotranscriptionally modified by the addition of a a cap structure, which consists of a 5&#8242; 7-methyl guanosine residue that protects the transcript from nuclease digestion and promotes translation. Additionally, eukaryotic mRNAs are 3\u2019-polyadenylated by a template independent polymerase. The poly(A) tail also functions in mRNA stability and translational regulation.<\/p>\n<p>For experiments where RNA will be introduced into cells by transfection or microinjection,\u00a0<em>in vitro<\/em>\u00a0transcripts can be modified to mimic mRNA by using the <a href=\"https:\/\/shop.neb-online.fr\/en\/art\/M2080@\" target=\"_blank\" rel=\"noopener noreferrer\">mRNA capping enzymes from vaccinia virus<\/a>\u00a0to add cap structures, and\u00a0<a href=\"https:\/\/shop.neb-online.fr\/en\/art\/M0276@\" target=\"_blank\" rel=\"noopener noreferrer\"><em>E. coli<\/em>\u00a0poly(A) polymerase<\/a>\u00a0to add poly(A) tails. Alternatively, cap structure analogs, such as <a href=\"https:\/\/shop.neb-online.fr\/en\/art\/S1404@\" target=\"_blank\" rel=\"noopener noreferrer\">(m7G(5&#8242;)ppp(5&#8242;)G)<\/a>, may be used to co-transcriptionally cap RNA transcripts during synthesis.<\/p>\n<p>Synthesized RNA can be used in a number of applications including RNA structure and function studies, ribozyme biochemistry, probes for RNase protection assays and hybridization based blots, anti-sense RNA and RNAi experiments, microarray analysis, microinjection,\u00a0<em>in vitro<\/em>\u00a0translation, and RNA vaccines.<\/p>\n<p>Please use our\u00a0<a href=\"https:\/\/international.neb.com\/tools-and-resources\/selection-charts\/rna-cap-analog-selection-chart\" target=\"_blank\" rel=\"noopener noreferrer\">RNA Cap Analog Selection Chart<\/a>\u00a0to find a suitable Cap Analog for your experiment.<\/p>\n<h3>RNA Clean-Up<\/h3>\n<p>After successful <em>in vitro<\/em>\u00a0transcription the template is degraded with\u00a0<a href=\"https:\/\/shop.neb-online.fr\/en\/art\/M0303@\" target=\"_blank\" rel=\"noopener noreferrer\">DNaseI<\/a>. mRNAs can be affinity purified with\u00a0<a href=\"https:\/\/www.neb-online.fr\/en\/art\/S1419S\" target=\"_blank\" rel=\"noopener noreferrer\">Oligo d(T)25 Magnetic Beads<\/a>.[\/vc_column_text][\/vc_column][\/vc_row]<\/p>\n<\/div>","protected":false},"excerpt":{"rendered":"<p>[vc_row][vc_column width=&#8221;1\/2&#8243;][vc_column_text] Background In vitro\u00a0synthesis of single-stranded RNA molecules is a routine laboratory procedure that is essential to the rapidly developing field of RNA research. This technique is versatile in that it allows the researcher to tailor synthesis, and introduce modifications that produce a transcript that is optimal for use in downstream applications. Though the&#8230;  <a class=\"excerpt-read-more\" href=\"https:\/\/www.neb-online.fr\/en\/rna-biology\/in-vitro-rna-synthesis\/\" title=\"Read In vitro RNA Synthesis\">Read more &raquo;<\/a><\/p>\n","protected":false},"author":15,"featured_media":1975,"parent":2191,"menu_order":0,"comment_status":"open","ping_status":"open","template":"page-sidebar-rna-biology.php","meta":{"footnotes":""},"class_list":["post-2193","page","type-page","status-publish","has-post-thumbnail","hentry"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.5 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>In vitro RNA Synthesis - New England Biolabs France<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.neb-online.fr\/en\/rna-biology\/in-vitro-rna-synthesis\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"In vitro RNA Synthesis - New England Biolabs France\" \/>\n<meta property=\"og:description\" content=\"[vc_row][vc_column width=&#8221;1\/2&#8243;][vc_column_text] Background In vitro\u00a0synthesis of single-stranded RNA molecules is a routine laboratory procedure that is essential to the rapidly developing field of RNA research. This technique is versatile in that it allows the researcher to tailor synthesis, and introduce modifications that produce a transcript that is optimal for use in downstream applications. Though the... 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This technique is versatile in that it allows the researcher to tailor synthesis, and introduce modifications that produce a transcript that is optimal for use in downstream applications. Though the... 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