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Rapid DNA Lib Prep Kit V2 HYD114

Rapid DNA Lib Prep Kit V2 contains the enzymes and buffers required to convert abroad range of input amounts of DNA into high quality libraries for next-generation sequencing on the Illumina® NGS platforms.Inputs of 1 ng to 1000 ng double-stranded DNA(dsDNA) are required for library preparation.

Cat No.: HYD114

Specification: 24T/96T

    Rapid DNA Lib Prep Kit V2 contains the enzymes and buffers required to convert abroad range of input amounts of DNA into high quality libraries for next-generation sequencing on the Illumina® NGS platforms.Inputs of 1 ng to 1000 ng double-stranded DNA(dsDNA) are required for library preparation. The entire four-step work flow takes place in a single tube or well, in about three hours(Figure 1). No intermediate purification steps or sample transfers are necessary, thus preventing handling errors and loss of valuable samples. Once purified and quantified, the resulting libraries are ready for Illumina NGS instruments using standard Illumina sequencing reagents and protocols. The kit provides excellent results for high-coverage deep sequencing, such as de novo sequencing, whole genome resequencing, whole exome sequencing, and other enrichment techniques.

    Reagent Composition

    Components

    24T

    96T

    End Preparation

    End Prep Buffer II

    168 μL

    672μL

    End Prep Enzymes

    72 μL

    288μL

    Adapter Ligation

    Ligation Buffer

    720 μL

    2880μL

    Ligase Enzymes II

    240 μL

    960μL

    Amplification

    2X PCR Mix

    600 μL

    2400μL

    10X ILM PCR Primers

    120 μL

    480 μL

    MGI PCR Primer Mix

    120 μL

    480 μL

    Storage Conditions

    All components should be stored at -20°C. The shelf life of each reagent is one year when stored properly.

    Notes

    Make sure to use high-quality DNA samples. Heavily nicked or damaged DNA will significantly lower library yield. We recommend Qubit® or other fluorometric methods to quantify DNA input. Residual trace RNA, nucleotides, ssDNAor other contaminants will decrease the efficiency of enzymes for optimized library preparation.

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