This product is a Small RNA sequencing library preparation kit designed for illumina's high-throughput sequencing platform, which can prepare Small RNA sequencing libraries starting from 1 ng~2 μg of Total RNA (containing Small RNA) or 1 ng~1 μg of enriched Small RNA for analyzing a wide range of small RNAs (including miRNA. piRNA, snoRNA and snRNA, etc.), piRNA, snoRNA and snRNA, etc.). Poly (A) Polymerase is used to add a Poly (A) tail to the 3’ end of the RNA, and Oligo (dT) primers with specific junctions are used for reverse transcription, which utilizes the terminal transferase activity of the reverse transcriptase to add specific junctions to the end of the cDNA. PCR amplification with primers for illumina sequencing junctions [e.g.BiorbytNext CDI Junction Primers (Illumina, for RNA libraries) (Code No. orb3229914, orb3229915, orb3229916)] were used to obtain small RNA libraries of 150 bp ~ 350 bp for illumina sequencing platform by magnetic bead sorting. The product is easy to operate, without the need to add illumina sequencing junctions and index sequences to obtain Small RNA libraries without the need to carry out tedious steps such as junction connection; the optimized reaction system improves the efficiency of library transformation, is compatible with different template amounts, and obtains stable sequencing results. This product contains all the components required for RNA 3’ end plus Poly (A) tail, reverse transcription (RT) and PCR amplification, the reaction system has been carefully optimized, all the reagents should be used in the experiments, it is not recommended to change the dosage and concentration of any reaction components or replace them with other equivalent products, in order to avoid obtaining bad results. If replacement is needed, please verify it first.
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Application Notes
1. For Illumina Sequencing Platform: Integrates Index and Illumina connectors to build Small RNA libraries that can be directly sequenced on the Illumina High-Throughput Sequencing Platform. 2. Wide range of templates: able to analyze a variety of Small RNAs including miRNA, piRNA, snoRNA and snRNA from 1 ng~2 μg Total RNA (containing Small RNA) or 1 ng~1 μg enriched Small RNA. 3. Low preference, easy to use, no need for tedious steps such as junctions to add illumina junctions and index sequences to obtain Small RNA sequencing libraries, avoiding the preferences associated with junction ligation.
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