RNA Seq Library Prep Kit

The RNA Seq Library Prep Kit, compatible with Illumina and MGI platforms, facilitates the creation of high-quality NGS libraries for next-generation sequencing. RNA sequencing, a potent tool for transcriptome analysis, enables studies on gene expression, transcription regulation, splicing, mutations, and variations. The kit requires purified RNA, such as rRNA-depleted RNA or polyA mRNA, as input. Library multiplexing is achievable with various index types. The kit's workflow offers three index options for Illumina platforms: non-index, index, and unique dual index, each with distinct capabilities and error identification features. Key features include a quick 2-hour protocol, minimal hands-on time, guaranteed high yield, uniform transcript coverage, and a simple workflow. The kit accommodates purified RNA inputs ranging from 3 ng to 100 ng. Comparative analyses demonstrate the kit's efficiency and uniform coverage. Additionally, it is part of a suite of related products.

• Purpose: High-quality NGS library construction for next-gen sequencing (Illumina & MGI platforms). RNA-seq for transcriptome analysis, including gene expression, regulation, splicing, mutations, and variations. Purified RNA input required
• Workflow: RNA Seq Library Prep Kit
• Index types for Illumina platforms:
• Non-indexed libraries (Illumina Cat.# 30055)
• Indexed libraries (Illumina Cat.# 30056): 6-base barcode, up to 48 samples, index info downloadable
• Unique dual-indexed libraries (Illumina Cat.# 30057): Up to 96 samples, 4-Base Difference Index System, error identification
• Indexes available for MGI platform kits (Cat.# 34112)
• Key Features
• Swift protocol: Libraries ready in 2 hours
• Minimal hands-on time (10 minutes)
• Guaranteed quality: High yield
• Uniform transcript coverage
• User-friendly workflow
• RNA input: 3 ng to 100 ng
• Protocol time comparison: BioDynami vs other vendors