[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"doc-seo-640396-105":3,"detail-sidebar-cat-0-en-105":80,"doc-detail-640396-en":130},{"code":4,"msg":5,"data":6},0,"ok",{"site_id":7,"language":8,"slug":9,"title":10,"keywords":11,"description":12,"schema_data":13,"social_meta":73,"head_meta":75,"extra_data":77,"updated_unix":79},105,"en","sbeadex-lightning-nucleic-acid-purification-chemistry-manual","sbeadex Lightning Nucleic Acid Purification Chemistry - Manual","","sbeadex Lightning nucleic acid purification chemistry manual provides an overview of the chemistry, modular kit system, and how to run automated nucleic acid purification workflows. It explains the superparamagnetic microparticles and one-step binding mechanism with water washing to remove impurities and inhibitors effectively. The document also links to sample-type specific laboratory protocols and includes guidance for automation, covering kit components, storage, experimental procedure, optimization for plant and livestock samples, and troubleshooting.",{"@graph":14,"@context":72},[15,34,55],{"@type":16,"itemListElement":17},"BreadcrumbList",[18,23,27,31],{"item":19,"name":20,"@type":21,"position":22},"https://docshare.wps.com","Home","ListItem",1,{"item":24,"name":25,"@type":21,"position":26},"https://docshare.wps.com/document/","Document",2,{"item":28,"name":29,"@type":21,"position":30},"https://docshare.wps.com/document/technology/","Technology",3,{"item":32,"name":10,"@type":21,"position":33},"https://docshare.wps.com/document/sbeadex-lightning-nucleic-acid-purification-chemistry-manual/640396/",4,{"url":32,"name":10,"@type":35,"image":36,"author":41,"headline":10,"publisher":44,"fileFormat":47,"inLanguage":8,"description":12,"dateModified":48,"datePublished":49,"encodingFormat":47,"isAccessibleForFree":50,"interactionStatistic":51},"DigitalDocument",{"url":37,"@type":38,"width":39,"height":40},"https://docshare.wps.com/thumbnails/sbeadex-lightning-nucleic-acid-purification-chemistry-manual/640396.png","ImageObject",300,407,{"name":42,"@type":43},"Đào","Person",{"url":19,"name":45,"@type":46},"DocShare","Organization","application/pdf","2026-10-26","2026-10-22",true,{"@type":52,"interactionType":53,"userInteractionCount":26},"InteractionCounter",{"@type":54},"ViewAction",{"@type":56,"mainEntity":57},"FAQPage",[58,64,68],{"name":59,"@type":60,"acceptedAnswer":61},"What is the main principle of sbeadex Lightning chemistry?","Question",{"text":62,"@type":63},"It uses superparamagnetic microparticles and a one-step binding mechanism, followed by a single water washing step to remove impurities and potential inhibitors.","Answer",{"name":65,"@type":60,"acceptedAnswer":66},"Which downstream applications are supported by the purified nucleic acids?",{"text":67,"@type":63},"The chemistry is described as suitable for PCR, qPCR, sequencing, NGS, and restriction analysis.",{"name":69,"@type":60,"acceptedAnswer":70},"How are the sbeadex Lightning kits organized?",{"text":71,"@type":63},"The system is modular, with two core kits (A and B) that contain different binding and elution components, plus additional lysis buffers and supplements provided for sample-specific protocols.","https://schema.org",{"og:url":32,"og:type":74,"og:title":10,"og:site_name":45,"og:description":12},"article",{"robots":76,"canonical":32},"index,follow",{"doc_id":78,"site_id":7},640396,1793051508,{"code":4,"msg":81,"data":82},"success",[83,87,91,95,100,104,109,114,119,122,126],{"id":22,"doc_module":4,"doc_module_name":25,"category_name":84,"show_sort_weight":85,"slug":86},"Story & Novel",90,"story-novel",{"id":26,"doc_module":4,"doc_module_name":25,"category_name":88,"show_sort_weight":89,"slug":90},"Literature",80,"literature",{"id":33,"doc_module":4,"doc_module_name":25,"category_name":92,"show_sort_weight":93,"slug":94},"Exam",70,"exam",{"id":96,"doc_module":4,"doc_module_name":25,"category_name":97,"show_sort_weight":98,"slug":99},5,"Comic",60,"comic",{"id":101,"doc_module":4,"doc_module_name":25,"category_name":29,"show_sort_weight":102,"slug":103},6,50,"technology",{"id":105,"doc_module":4,"doc_module_name":25,"category_name":106,"show_sort_weight":107,"slug":108},7,"Healthcare",40,"healthcare",{"id":110,"doc_module":4,"doc_module_name":25,"category_name":111,"show_sort_weight":112,"slug":113},8,"Research & Report",30,"research-report",{"id":115,"doc_module":4,"doc_module_name":25,"category_name":116,"show_sort_weight":117,"slug":118},9,"Religion & Spirituality",20,"religion-spirituality",{"id":117,"doc_module":4,"doc_module_name":25,"category_name":120,"show_sort_weight":117,"slug":121},"World Cup","world-cup",{"id":123,"doc_module":4,"doc_module_name":25,"category_name":124,"show_sort_weight":123,"slug":125},10,"Lifestyle","lifestyle",{"id":127,"doc_module":4,"doc_module_name":25,"category_name":128,"show_sort_weight":96,"slug":129},19,"General","general",{"code":4,"msg":81,"data":131},{"doc_id":78,"user_id":132,"nickname":42,"user_avatar":133,"doc_module":4,"category_id":101,"category_name":29,"doc_title":10,"doc_description":12,"doc_content":134,"file_id":135,"file_url":136,"file_type":137,"file_size":138,"view_count":26,"is_deleted":4,"is_public":22,"is_downloadable":22,"audit_status":22,"page_count":139,"language":140,"language_code":8,"site_id":7,"html_lang":8,"table_of_contents":141,"faqs":142,"seo_title":143,"seo_description":12,"update_tm":144,"read_time":145},1374402968488,"https://ap-avatar.wpscdn.com/davatar_29158cc5080c5b710cf443261637dec0","Manual  \nsbeadex Lightning nucleic acid purification chemistry  \nFor Research Use Only. Not for use in diagnostic procedures.  \nManual  \nsbeadex Lightning nucleic acid purification chemistry  \nContents  \n1. Purpose of this document................................................................................................................3  \n2. Introduction to sbeadex Lightning chemistry................................................................................3  \n3. Kit contents and storage conditions...............................................................................................4  \n4. Experimental procedure ...................................................................................................................5  \n4.1 General information before starting ......................................................................................5  \n4.2 Lysis recommendations ..........................................................................................................6  \n4.2.1 Plant ...............................................................................................................................6  \n4.2.2 Livestock .......................................................................................................................6  \n4.3 Optimising input volume.........................................................................................................6  \n4.3.1 Plant samples................................................................................................................6  \n4.3.2 Livestock samples........................................................................................................7  \n4.4 Magnets and alternatives ........................................................................................................7  \n4.5 Particle resuspension..............................................................................................................7  \n4.6 Formation of precipitates in lysis buffers .............................................................................7  \n4.7 Coloration of binding buffer and precipitates ......................................................................7  \n4.8 Laboratory conditions ............................................................................................................7  \n4.9 Required materials (not included) ..........................................................................................8  \n4.10 Disruption and homogenisation of plant materials .............................................................8  \n5. Automation ........................................................................................................................................9  \n6. Protocols ...........................................................................................................................................9  \n7. Troubleshooting ..............................................................................................................................10  \n8. Frequently asked questions...........................................................................................................10  \n9. Further support ...............................................................................................................................10  \n2  \nFor Research Use Only. Not for use in diagnostic procedures.  \nManual  \nsbeadex Lightning nucleic acid purification chemistry  \n1. Purpose of this document  \nThe purpose of this document is to provide a general introduction to sbeadex ™ Lightning nucleic acid  purification chemistry and universal details about how to run sbeadex Lightning in your laboratory. The document also contains links to specific laboratory protocols required to perform nucleic acid purification from different sample types, and information and guidance on the automation of protocols.  \n2. Introduction to sbeadex Lightning chemistry  \nsbea","cbCail3tOw6XAdSw","https://ap.wps.com/l/cbCail3tOw6XAdSw","pdf",403654,11,"English","# Purpose of this document\n# Introduction to sbeadex Lightning chemistry\n# Kit contents and storage conditions\n# Experimental procedure\n## General information before starting\n## Lysis recommendations\n## Optimising input volume\n## Magnets and alternatives\n## Particle resuspension\n## Formation of precipitates in lysis buffers\n## Coloration of binding buffer and precipitates\n## Laboratory conditions\n## Required materials (not included)\n## Disruption and homogenisation of plant materials\n# Automation\n# Protocols\n# Troubleshooting\n# Frequently asked questions\n# Further support","[{\"question\":\"What is the main principle of sbeadex Lightning chemistry?\",\"answer\":\"It uses superparamagnetic microparticles and a one-step binding mechanism, followed by a single water washing step to remove impurities and potential inhibitors.\"},{\"question\":\"Which downstream applications are supported by the purified nucleic acids?\",\"answer\":\"The chemistry is described as suitable for PCR, qPCR, sequencing, NGS, and restriction analysis.\"},{\"question\":\"How are the sbeadex Lightning kits organized?\",\"answer\":\"The system is modular, with two core kits (A and B) that contain different binding and elution components, plus additional lysis buffers and supplements provided for sample-specific protocols.\"}]","sbeadex Lightning Nucleic Acid Purification Chemistry - Manual | PDF",1792708946,28]