CN EN
P
产品中心
Product center
产品中心
Product center
  • NEXTFLEX® 16S V4 and 18S Amplicon-Seq Kit

    NEXTFLEX® 16S V4 and 18S Amplicon-Seq Kit

    The NEXTFLEX® 16S V4 and 18S Amplicon-Seq Kit is designed to prepare libraries that cover both the V4 hypervariable domain of the 16S rRNA genes present in microbial populations and the 18S regions that can identify fungal and micro-eukaryotic organisms in a single library prep.

    查看详情 +
  • NEXTFLEX® Combo-Seq™ mRNA/miRNA Kit

    NEXTFLEX® Combo-Seq™ mRNA/miRNA Kit

    The NEXTFLEX® Combo-Seq™ Kit enables the user to generate combined mRNA and small RNA libraries in a single workflow using 5 ng – 100 ng of total RNA inputs, without requiring upfront costly and tedious rRNA depletion or poly(A) selection.

    查看详情 +
  • NEXTFLEX Small RNA-seq v3 Kit with UDIs

    NEXTFLEX Small RNA-seq v3 Kit with UDIs

    The NEXTFLEX® small RNA-seq v3 kit with UDIs uses the same popular chemistry of the NEXTFLEX small RNA-seq kit v3, which incorporates technologies that reduce small RNA ligation bias, increase ligation efficiency, reduce adapter-dimer formation, and build in a new dimension of data quality, integrity, and accuracy with the integration of Unique Dual Indexes (UDIs) for Illumina® sequencing on the MiSeq®, HiSeq® 2000/2500, and NovaSeq® platforms.

    查看详情 +
  • NEXTFLEX® Rapid Directional RNA-Seq Kit 2.0

    NEXTFLEX® Rapid Directional RNA-Seq Kit 2.0

    The NEXTFLEX® rapid directional RNA-seq kit 2.0 produces libraries for Illumina® sequencing instruments with high coverage uniformity, low duplication rates, strand specificity and minimal rRNA contamination when used with the NEXTFLEX® Poly(A) Beads 2.0 (10 ng – 5 μg) or NEXTFLEX® RiboNaut™ rRNA depletion kit (human, mouse, rat) (5 ng – 1 μg).

    查看详情 +
  • NEXTFLEX® Rapid XP DNA-Seq Kit

    NEXTFLEX® Rapid XP DNA-Seq Kit

    The NEXTFLEX® Rapid XP DNA-Seq kit combines enzymatic fragmentation with end-repair and A-tailing in one reaction to create a highly efficient first step in library generation, which is followed by ligation and PCR (optional for PCR-free workflows). This effective one-tube workflow produces DNA-seq libraries with consistent library size, high yield, low GC-bias, and high coverage.

    查看详情 +
TOP